Posts belonging to Category 'Ulcerative Colitis Crohn's'

War Is Not The World's Greatest Evil–Not Even Close

Question:

The Twelve Most Frequently Asked Questions about Colon Hydrotherapy 1. Is colon hydrotherapy safe? Yes. In fact with new colon therapy equipment, treatments are much safer than the common enema. 2. How does a colon hydrotherapy treatment compare to an enema? An enema only reaches the rectum and lower part of the colon, whereas with colon hydrotherapy, the entire length of the colon (the large intestinal tract approximately 5 to 5

Absorb Plus (Elemental Diet)

Question:

Thanks :-)

– Hide quoted text — Show quoted text – I think you did a FINE job! Well, at least I understood what you were trying to say. Debs Hi, as far as * I understand * Elemental diets are broken down into amino acids (from proteins) etc so that your intestines don’t have to do any work. I was on them for 6 months, but it was so hard not to eat anything else and only drink water! I now have Fortisip which are still drinks, but as I can now eat these just help provide extra calories – these drinks are  not broken down. When I was on the Elemental diet I had a Fortisip, which then put me in hospital as they then inflamed my intestines . Are you sure this drink is an Elemental diet drink, and not like a Fortisip? Since it contains proteins your intestines have to work to break them down into amino acids for your body to absorb. Are you supposed to be on an Elemental diet? If you are, I would check with your doctor as there could be a  difference between the two Mel :-) I’m know that there are some of you out there could help me out in explaining this properly!! yes… I’ve tried it…I didn’t care for it to much…taste…still have some to use up! I was just wondering if anyone has used this product for ulcerative colitis, Crohn’s or any other digestive ailments. It’s recommended in the book "The IBD Remission Diet" by Jini Patel Thompson (who is also the author of "Listen to Your Gut"). This is a product she created, because she wasn’t happy with any of the elemental diets available, as they had a lot of sugar and bad fats, etc. I ordered some and had high hopes. However, I merely sampled it and didn’t seem to react well. A main ingredient is Whey Protein Isolate and it’s 99.8% lactose free, so I don’t understand why and wonder if I should try it again. Knowing what anyone else has experienced would be very helpful indeed. Any feedback will be very appreciated. Thank you. Suzan

Response:

Suzan, I have no experience with elemental diets, but I don’t tolerate milk-based supplements. Whey protein isolate is a milk protein. Although it is lactose-free, it still is milk so this may be a problem if you don’t tolerate dairy. Talking to a dietitian may be helpful if you can’t tolerate certain foods. Take care, Amy. – Hide quoted text — Show quoted text – I was just wondering if anyone has used this product for ulcerative colitis, Crohn’s or any other digestive ailments. It’s recommended in the book "The IBD Remission Diet" by Jini Patel Thompson (who is also the author of "Listen to Your Gut"). This is a product she created, because she wasn’t happy with any of the elemental diets available, as they had a lot of sugar and bad fats, etc. I ordered some and had high hopes. However, I merely sampled it and didn’t seem to react well. A main ingredient is Whey Protein Isolate and it’s 99.8% lactose free, so I don’t understand why and wonder if I should try it again. Knowing what anyone else has experienced would be very helpful indeed. Any feedback will be very appreciated. Thank you. Suzan

Response:

Hi Mel, As far as I know, it’s an elemental diet, meant to give the bowels a total rest. It can be used as a supplement to add calories to one’s regular food if necessary, but it was developed to be an alternative to drugs like prednisone or surgery. Here’s something I’m copying from the info I have that will perhaps clarify better: Thanks, Suzan How was Absorb Plus Formulated?        Absorb Plus was formulated by Jini Patel Thompson, the author of LISTEN TO YOUR GUT: Natural Healing & Dealing With Inflammatory Bowel Disease & Irritable Bowel Syndrome.   After a bout of severe intestinal haemorrhaging, Jini’s weight dropped to 99 pounds (she’s 5′7") and her albumin levels showed she was severely malnourished. After receiving a blood transfusion, her doctor advised complete bowel rest – to allow the intestine heal. Continuing to eat regular food simply re-opened the wounds and started the bleeding again. Therefore, her nutrition needed to come from a completely elemental (pre-digested) liquid source.    Jini tried each of the elemental (pre-digested) products provided by the hospital, but found the taste and ingredient list unacceptable. Rather than undergoing an operation to have a tube inserted in her stomach and the elemental products pumped in, she set out to find a natural, healthy, alternative.    After an extensive search of health stores and the Internet, Jini devised her own elemental formula by mixing together 6 different products. She did this 8-9 times a day to give her body the nutrients it needed in elemental (pre-digested for maximum absorption) form. Using this formula, Jini gained 36 pounds of solid weight (not fat) in six weeks and her albumin levels were restored to normal. She went from being so weak she could barely move around her apartment, to cycling and lifting weights at the gym by the end of the six weeks at a healthy weight of 135 pounds.    Jini included directions for mixing up these elemental shakes in the first edition of her book LISTEN TO YOUR GUT (Caramal Publishing 2000). In addition, as word spread through family and friends, people with a variety of afflictions (cancer/chemotherapy, trigeminal neuralgia, age-related malnutrition and loss of appetite, etc.) began contacting Jini for her weight gain and maintenance program. However, many of these people and her readers commented that they found it too difficult and time-consuming to mix together so many different products. Having done it herself, Jini could sympathise with them! Fortunately, a year later, she met one of the founders of  and he asked her to replicate her formula in one product. She happily agreed and the result is Absorb Plus.    We know of no other product comparable to Absorb Plus in quality and composition, that is also elemental (pre-digested for maximum absorption). In addition, our own trials, and letters from our customers show that Absorb Plus really works. – Hide quoted text — Show quoted text – Hi, as far as * I understand * Elemental diets are broken down into amino acids (from proteins) etc so that your intestines don’t have to do any work. I was on them for 6 months, but it was so hard not to eat anything else and only drink water! I now have Fortisip which are still drinks, but as I can now eat these just help provide extra calories – these drinks are  not broken down. When I was on the Elemental diet I had a Fortisip, which then put me in hospital as they then inflamed my intestines . Are you sure this drink is an Elemental diet drink, and not like a Fortisip? Since it contains proteins your intestines have to work to break them down into amino acids for your body to absorb. Are you supposed to be on an Elemental diet? If you are, I would check with your doctor as there could be a  difference between the two Mel :-) I’m know that there are some of you out there could help me out in explaining this properly!! yes… I’ve tried it…I didn’t care for it to much…taste…still have some to use up! I was just wondering if anyone has used this product for ulcerative colitis, Crohn’s or any other digestive ailments. It’s recommended in the book "The IBD Remission Diet" by Jini Patel Thompson (who is also the author of "Listen to Your Gut"). This is a product she created, because she wasn’t happy with any of the elemental diets available, as they had a lot of sugar and bad fats, etc. I ordered some and had high hopes. However, I merely sampled it and didn’t seem to react well. A main ingredient is Whey Protein Isolate and it’s 99.8% lactose free, so I don’t understand why and wonder if I should try it again. Knowing what anyone else has experienced would be very helpful indeed. Any feedback will be very appreciated. Thank you. Suzan

Response:

I think you did a FINE job! Well, at least I understood what you were trying to say. Debs – Hide quoted text — Show quoted text – Hi, as far as * I understand * Elemental diets are broken down into amino acids (from proteins) etc so that your intestines don’t have to do any work. I was on them for 6 months, but it was so hard not to eat anything else and only drink water! I now have Fortisip which are still drinks, but as I can now eat these just help provide extra calories – these drinks are  not broken down. When I was on the Elemental diet I had a Fortisip, which then put me in hospital as they then inflamed my intestines . Are you sure this drink is an Elemental diet drink, and not like a Fortisip? Since it contains proteins your intestines have to work to break them down into amino acids for your body to absorb. Are you supposed to be on an Elemental diet? If you are, I would check with your doctor as there could be a  difference between the two Mel :-) I’m know that there are some of you out there could help me out in explaining this properly!! yes… I’ve tried it…I didn’t care for it to much…taste…still have some to use up! I was just wondering if anyone has used this product for ulcerative colitis, Crohn’s or any other digestive ailments. It’s recommended in the book "The IBD Remission Diet" by Jini Patel Thompson (who is also the author of "Listen to Your Gut"). This is a product she created, because she wasn’t happy with any of the elemental diets available, as they had a lot of sugar and bad fats, etc. I ordered some and had high hopes. However, I merely sampled it and didn’t seem to react well. A main ingredient is Whey Protein Isolate and it’s 99.8% lactose free, so I don’t understand why and wonder if I should try it again. Knowing what anyone else has experienced would be very helpful indeed. Any feedback will be very appreciated. Thank you. Suzan

Response:

I was just wondering if anyone has used this product for ulcerative colitis, Crohn’s or any other digestive ailments. It’s recommended in the book "The IBD Remission Diet" by Jini Patel Thompson (who is also the author of "Listen to Your Gut"). This is a product she created, because she wasn’t happy with any of the elemental diets available, as they had a lot of sugar and bad fats, etc. I ordered some and had high hopes. However, I merely sampled it and didn’t seem to react well. A main ingredient is Whey Protein Isolate and it’s 99.8% lactose free, so I don’t understand why and wonder if I should try it again. Knowing what anyone else has experienced would be very helpful indeed. Any feedback will be very appreciated. Thank you. Suzan

Response:

yes… I’ve tried it…I didn’t care for it to much…taste…still have some to use up!

– Hide quoted text — Show quoted text – I was just wondering if anyone has used this product for ulcerative colitis, Crohn’s or any other digestive ailments. It’s recommended in the book "The IBD Remission Diet" by Jini Patel Thompson (who is also the author of "Listen to Your Gut"). This is a product she created, because she wasn’t happy with any of the elemental diets available, as they had a lot of sugar and bad fats, etc. I ordered some and had high hopes. However, I merely sampled it and didn’t seem to react well. A main ingredient is Whey Protein Isolate and it’s 99.8% lactose free, so I don’t understand why and wonder if I should try it again. Knowing what anyone else has experienced would be very helpful indeed. Any feedback will be very appreciated. Thank you. Suzan

Response:

Hi, as far as * I understand * Elemental diets are broken down into amino acids (from proteins) etc so that your intestines don’t have to do any work. I was on them for 6 months, but it was so hard not to eat anything else and only drink water! I now have Fortisip which are still drinks, but as I can now eat these just help provide extra calories – these drinks are  not broken down. When I was on the Elemental diet I had a Fortisip, which then put me in hospital as they then inflamed my intestines . Are you sure this drink is an Elemental diet drink, and not like a Fortisip? Since it contains proteins your intestines have to work to break them down into amino acids for your body to absorb. Are you supposed to be on an Elemental diet? If you are, I would check with your doctor as there could be a  difference between the two Mel :-) I’m know that there are some of you out there could help me out in explaining this properly!!

– Hide quoted text — Show quoted text – yes… I’ve tried it…I didn’t care for it to much…taste…still have some to use up! I was just wondering if anyone has used this product for ulcerative colitis, Crohn’s or any other digestive ailments. It’s recommended in the book "The IBD Remission Diet" by Jini Patel Thompson (who is also the author of "Listen to Your Gut"). This is a product she created, because she wasn’t happy with any of the elemental diets available, as they had a lot of sugar and bad fats, etc. I ordered some and had high hopes. However, I merely sampled it and didn’t seem to react well. A main ingredient is Whey Protein Isolate and it’s 99.8% lactose free, so I don’t understand why and wonder if I should try it again. Knowing what anyone else has experienced would be very helpful indeed. Any feedback will be very appreciated. Thank you. Suzan

Response:

Social Security Disability…..

Question:

Thanks Doc! Christine UC Class of 01

– Hide quoted text — Show quoted text – RE: Re: Social Security Disability….. My first thought is to say a big THANK YOU to Margie for providing a web site and phone number for a company that may be able to help out many people here!  Lots of people have problems with SSD and need all the help they can get.  Also, IMHO the best way to find assistance with this and other things is from a personal recommendation.  Just like with a doctor, a hair dresser, a repair person, etc; a referral from a friend is invaluable. While I haven’t been on the ng for that long, I have noticed that Margie is one person who always had good advice and a kind word.  This is a support group and Margie is very supportive! I think it’s high time all the flaming and sniping stopped!  As far as going back several years and dragging out parts of old posts – WHO CARES?! Let’s just stop it all and go back to being a SUPPORT group. Christine UC Class of 01 – I was trying to compose something along these lines, but couldn’t get it right.  You did.  Thank You for saying what some of us feel. – – Origin: The Wild Wild West * 503-623-0185

Response:

Did you ever think she forgot with all the meds she is on and on the illness she has?

The question of kickbacks goes to the issue of credibility. When you’re considering buying a house, you first get it checked out thoroughly by a professional inspector. You could use an inspector your realtor recommends, but remember that your realtor probably has her eyes firmly on her commission, so she may well recommend an inspector she knows will give you a report that makes the house sound fine. It’s far smarter to get an inspector who has no vested interest in either the present transaction or an ongoing relationship with the realtor. Same thing with USANA. Ken only gives endorsements from doctors who are either on the USANA payroll or who have some mutual product-endorsement deal with the company. If he quoted doctors who have absolutely no connection with USANA whatsoever, he’d gain cridibility. None of this is to say that Allsup is necessarily bad. It may be full of brilliant lawyers. But you should reach that conclusion based on information that is objective, fairly measured, and not vulnerable to accusations of conflict of interest.

Response:

RE: Re: Social Security Disability….. My first thought is to say a big THANK YOU to Margie for providing a web site and phone number for a company that may be able to help out many people here!  Lots of people have problems with SSD and need all the help they can get.  Also, IMHO the best way to find assistance with this and other things is from a personal recommendation.  Just like with a doctor, a hair dresser, a repair person, etc; a referral from a friend is invaluable. While I haven’t been on the ng for that long, I have noticed that Margie is one person who always had good advice and a kind word.  This is a support group and Margie is very supportive! I think it’s high time all the flaming and sniping stopped!  As far as going back several years and dragging out parts of old posts – WHO CARES?! Let’s just stop it all and go back to being a SUPPORT group. Christine UC Class of 01

- I was trying to compose something along these lines, but couldn’t get it right.  You did.  Thank You for saying what some of us feel. – – Origin: The Wild Wild West * 503-623-0185

Response:

I don’t post very often in here, but I’m always lurking. I think it’s very sad that someone whose helped ALOT of people is getting picked apart the way she is. I’ve seen it happen in here too many times. If you’re not going to help someone why come in here and make trouble? This tells me some people have nothing better to do with their time. I’m hoping Margie stays here because she is one of the people I’ve seen post to help others and her post do count and they do help. Just my 2 cents.

– Hide quoted text — Show quoted text – My first thought is to say a big THANK YOU to Margie for providing a web site and phone number for a company that may be able to help out many people here!  Lots of people have problems with SSD and need all the help they can get.  Also, IMHO the best way to find assistance with this and other things is from a personal recommendation.  Just like with a doctor, a hair dresser, a repair person, etc; a referral from a friend is invaluable. While I haven’t been on the ng for that long, I have noticed that Margie is one person who always had good advice and a kind word.  This is a support group and Margie is very supportive! I think it’s high time all the flaming and sniping stopped!  As far as going back several years and dragging out parts of old posts – WHO CARES?! Let’s just stop it all and go back to being a SUPPORT group. Christine UC Class of 01 Did you ever think she forgot with all the meds she is on and on the illness she has?  This is down right mean NA.  For the rest of you if you go to the link supplied start at the beginning of the thread so you get the whole picture of this thread.   I am very sad that people who need support are getting trashed.  Why?  Can you answer me this because I don’t understand. With all the meds and medical stuff I have gone through in the last three years I am happy when I remember the last time I ate or what it was.  I forget daily stuff never mind stuff back too the year 2000.  UM MOM Susan I had no idea that one could recieve moneies for sending people their way.  Newsgroups: alt.support.crohns-colitis Dear Ken:   Congratulations!  By the way, to anyone who uses or used Allsup at my reccommendation, ***please give them my name.***  I have been reccommending them ever since my approval and did not find out about the referral thing until the other day!  So, I would appreciate it if you guys would give my name, Marjorie Olige, if you do decide to use them.  They are the best!  I know this sounds cheesy, but  ***I could use any monies I could get!***  Thanks.  And Ken I know you must be as happy as I was.  I did have to go through the hearing, but it wasn’t as bad as I was afraid it might be.  In fact, my case worker gave all the information to the judge, he then asked me a few questions and it was all over in less than a half an hour!  I was so thrilled to finally be approved!  My very first filing with SS was over 20 years ago when they told me to retrain, which I did and found I was able to go back to work.  In fact I was able to fulfill my dream of nursing at that time, so I guess they were right. But when I could no longer work under any circumstances, I finally went through Allsup, due to a TV commercial I saw, and they handled it all!  It took almost 2 years, but it sure was worth it!  I think they are wonderful!  Well, let me get off my soap box here and let you all get on about your business.  Ken, I wish you wellness. Love,   Margie CD Class of 67 UC Class of 96 [original post:

http://groups.google.com/groups?q=marjorie+allsup+group:alt.support.c... olitis&hl=en&lr=&ie=UTF-8&selm=20000506191645.05274.00001242%40ng-cq1.aol.c o - Hide quoted text -- Show quoted text - m&rnum=1]

Response:

I’m amazed that Perry seems to have enough time at work to read all the current posts as well as all the ones from 3 years ago — I want *his* job! Hey Sue — how about the ng charter again???? This is supposed to be a support group and I know that over the last 5 years, Margie has been a wonderful source of support for me! Perhaps others here need to remember that. Rebecca :-)

What is Alt.support.crohns-colitis? Alt.support.crohns-colitis was created in early 1994 as a forum where people suffering from ulcerative colitis, Crohn’s Disease, and irritable bowel syndrome can share their everyday struggles with these illnesses, as well as discuss medicines, treatments, surgery, diet, health care providers, related illnesses, and anything else anyone can think of that relates to these diseases.  In other words, this is the online equivalent of a support group, which means that no question is stupid and no condition embarrassing here.  It also means we’re all here to help each other out, so please be nice, be polite, and no flaming. Discussions of all types of medicine- conventional and alternative, Western and Eastern, your Aunt Harriet’s home remedies, whatever- are welcome here; however, any person discussing a potential remedy which he or she also sells must explicitly begin the "Subject" header of their post with the word "AD" or "ADVERTISEMENT" in all caps, regardless of whether or not they profit from such sales.  Spamming is expressly forbidden as violating the rules of netiquette as well as those of this newsgroup.  Finally, please keep in mind that no one knows what causes these illnesses, no one’s come up with a cure, and we need all the help we can get.

Response:

My first thought is to say a big THANK YOU to Margie for providing a web site and phone number for a company that may be able to help out many people here!  Lots of people have problems with SSD and need all the help they can get.  Also, IMHO the best way to find assistance with this and other things is from a personal recommendation.  Just like with a doctor, a hair dresser, a repair person, etc; a referral from a friend is invaluable. While I haven’t been on the ng for that long, I have noticed that Margie is one person who always had good advice and a kind word.  This is a support group and Margie is very supportive! I think it’s high time all the flaming and sniping stopped!  As far as going back several years and dragging out parts of old posts – WHO CARES?! Let’s just stop it all and go back to being a SUPPORT group. Christine UC Class of 01

– Hide quoted text — Show quoted text – Did you ever think she forgot with all the meds she is on and on the illness she has?  This is down right mean NA.  For the rest of you if you go to the link supplied start at the beginning of the thread so you get the whole picture of this thread.   I am very sad that people who need support are getting trashed.  Why?  Can you answer me this because I don’t understand. With all the meds and medical stuff I have gone through in the last three years I am happy when I remember the last time I ate or what it was.  I forget daily stuff never mind stuff back too the year 2000.  UM MOM Susan I had no idea that one could recieve moneies for sending people their way.  Newsgroups: alt.support.crohns-colitis Dear Ken:   Congratulations!  By the way, to anyone who uses or used Allsup at my reccommendation, ***please give them my name.***  I have been reccommending them ever since my approval and did not find out about the referral thing until the other day!  So, I would appreciate it if you guys would give my name, Marjorie Olige, if you do decide to use them.  They are the best!  I know this sounds cheesy, but  ***I could use any monies I could get!***  Thanks.  And Ken I know you must be as happy as I was.  I did have to go through the hearing, but it wasn’t as bad as I was afraid it might be.  In fact, my case worker gave all the information to the judge, he then asked me a few questions and it was all over in less than a half an hour!  I was so thrilled to finally be approved!  My very first filing with SS was over 20 years ago when they told me to retrain, which I did and found I was able to go back to work.  In fact I was able to fulfill my dream of nursing at that time, so I guess they were right. But when I could no longer work under any circumstances, I finally went through Allsup, due to a TV commercial I saw, and they handled it all!  It took almost 2 years, but it sure was worth it!  I think they are wonderful!  Well, let me get off my soap box here and let you all get on about your business.  Ken, I wish you wellness. Love,   Margie CD Class of 67 UC Class of 96 [original post:

http://groups.google.com/groups?q=marjorie+allsup+group:alt.support.c... olitis&hl=en&lr=&ie=UTF-8&selm=20000506191645.05274.00001242%40ng-cq1.aol.c o - Hide quoted text -- Show quoted text - m&rnum=1]

Response:

Very well said Rebecca.  Margie has been very giving in her support of all of us.  And I will continue to support her. — Take Care, Sherry  :o) (To reply remove nospam from addie.)

– Hide quoted text — Show quoted text – I’m amazed that Perry seems to have enough time at work to read all the current posts as well as all the ones from 3 years ago — I want *his* job! Hey Sue — how about the ng charter again???? This is supposed to be a support group and I know that over the last 5 years, Margie has been a wonderful source of support for me! Perhaps others here need to remember that. Rebecca :-) Did you ever think she forgot with all the meds she is on and on the illness she has?  This is down right mean NA.  For the rest of you if you go to the link supplied start at the beginning of the thread so you get the whole picture of this thread.   I am very sad that people who need support are getting trashed.  Why?  Can you answer me this because I don’t understand. With all the meds and medical stuff I have gone through in the last three years I am happy when I remember the last time I ate or what it was.  I forget daily stuff never mind stuff back too the year 2000.  UM MOM Susan I had no idea that one could recieve moneies for sending people their way.  Newsgroups: alt.support.crohns-colitis Dear Ken:   Congratulations!  By the way, to anyone who uses or used Allsup at my reccommendation, ***please give them my name.***  I have been reccommending them ever since my approval and did not find out about the referral thing until the other day!  So, I would appreciate it if you guys would give my name, Marjorie Olige, if you do decide to use them.  They are the best!  I know this sounds cheesy, but  ***I could use any monies I could get!***  Thanks.  And Ken I know you must be as happy as I was.  I did have to go through the hearing, but it wasn’t as bad as I was afraid it might be.  In fact, my case worker gave all the information to the judge, he then asked me a few questions and it was all over in less than a half an hour!  I was so thrilled to finally be approved!  My very first filing with SS was over 20 years ago when they told me to retrain, which I did and found I was able to go back to work.  In fact I was able to fulfill my dream of nursing at that time, so I guess they were right. But when I could no longer work under any circumstances, I finally went through Allsup, due to a TV commercial I saw, and they handled it all!  It took almost 2 years, but it sure was worth it!  I think they are wonderful!  Well, let me get off my soap box here and let you all get on about your business.  Ken, I wish you wellness. Love,   Margie CD Class of 67 UC Class of 96 [original post:

http://groups.google.com/groups?q=marjorie+allsup+group:alt.support.c... olitis&hl=en&lr=&ie=UTF-8&selm=20000506191645.05274.00001242%40ng-cq1.aol.c o m&rnum=1]

— Outgoing mail is certified Virus Free. Checked by AVG anti-virus system (http://www.grisoft.com).

Response:

Ditto! Debs – Hide quoted text — Show quoted text – I’m amazed that Perry seems to have enough time at work to read all the current posts as well as all the ones from 3 years ago — I want *his* job! Hey Sue — how about the ng charter again???? This is supposed to be a support group and I know that over the last 5 years, Margie has been a wonderful source of support for me! Perhaps others here need to remember that. Rebecca :-) Did you ever think she forgot with all the meds she is on and on the illness she has?  This is down right mean NA.  For the rest of you if you go to the link supplied start at the beginning of the thread so you get the whole picture of this thread.   I am very sad that people who need support are getting trashed.  Why?  Can you answer me this because I don’t understand. With all the meds and medical stuff I have gone through in the last three years I am happy when I remember the last time I ate or what it was.  I forget daily stuff never mind stuff back too the year 2000.  UM MOM Susan I had no idea that one could recieve moneies for sending people their way.  Newsgroups: alt.support.crohns-colitis Dear Ken:   Congratulations!  By the way, to anyone who uses or used Allsup at my reccommendation, ***please give them my name.***  I have been reccommending them ever since my approval and did not find out about the referral thing until the other day!  So, I would appreciate it if you guys would give my name, Marjorie Olige, if you do decide to use them.  They are the best!  I know this sounds cheesy, but  ***I could use any monies I could get!***  Thanks.  And Ken I know you must be as happy as I was.  I did have to go through the hearing, but it wasn’t as bad as I was afraid it might be.  In fact, my case worker gave all the information to the judge, he then asked me a few questions and it was all over in less than a half an hour!  I was so thrilled to finally be approved!  My very first filing with SS was over 20 years ago when they told me to retrain, which I did and found I was able to go back to work.  In fact I was able to fulfill my dream of nursing at that time, so I guess they were right. But when I could no longer work under any circumstances, I finally went through Allsup, due to a TV commercial I saw, and they handled it all!  It took almost 2 years, but it sure was worth it!  I think they are wonderful!  Well, let me get off my soap box here and let you all get on about your business.  Ken, I wish you wellness. Love,   Margie CD Class of 67 UC Class of 96 [original post: http://groups.google.com/groups?q=marjorie+allsup+group:alt.support.c... olitis&hl=en&lr=&ie=UTF-8&selm=20000506191645.05274.00001242%40ng-cq1.aol.c o m&rnum=1]

Response:

Does it (and should it) really make any difference to anyone whether or not the person giving info about an organisation  that may be of assistance to another gets a kickback?  The ONLY point should be does this mob or do they not provide assistance as suggested by the one passing their name on. Surely if the help is there, and you take advantage of it, there can be no reason for the source of your help getting something in return. Greg – Hide quoted text — Show quoted text – Last I checked, they also had an informative website at www.allsupinc.com.  There are several people on the ng who have obtained SSD using their services. To All I Promised This Number To:   This is the only reason I am posting right now.  I have promised some of you guys that I would get that number for you for the company that helped me.  I hope they can help you as well.  If it means anything to you, I get NOTHING, NOTHING, NOTHING for passing this number on except the good feeling that I may have helped someone.  So…anyway the name of the company is Allsup Inc and the number I have for them is 1-800-854-1418.  They are open from 8am to 5pm Central Time.  I wish you all well and I hope this helps.  Many of you are still on my prayer list.  Some of you I have come to dearly care about.  So stay well, and God bless. Love,  Margie CD Class of 67 UC Class of 96

Response:

At this very moment I’m very upset, what’s going on the group and especially a very good sweet person being under attack, I’m proud to say she’s my friend!!!. I haven’t posted for a long time to the NG, though I’ve been following the posts and responses, especially, this thread and the other one were Margie has been attacked several times for no reason at all!! For some strange reason I thought this was supposed to be a supportive group for people who have UC/CD their families and to share our personal experience. As we know example: one treatment may work for one person, the next person it won’t work at all, that’s not a reason to totally disrepect, and say nasty things. I totally don’t understand why all these attacks, flaming wars etc, are coming from and why they are happenning. I’m asking please respect each other, we’re a very big family, some of us know each other since the NG started!!! For the new people who are joining the NG, give us some time, to get to know us, much better!!! I totally agree with Susan!!! Margie has been a good, supportive friend, personally I have talked to her several times on the phone, while I was admitted in hospital with a small/large bowel obstruction, last year, away from my family, friends…she would call, to see how I was doing, some days, I was feeling so bad, she was always there for me if I needed to talk or cry!!!she’s the sweetest person you want to have for a friend. I have built great relationships with other friends too, on the NG. Margie, needs this support group & her friends, too support her whether she’s feeling better, having a good or bad day and share information as some of you may know with this disease you might be feeling great one day and the next day everything goes down hill!!! As far as I know Margie posted this message, in the intentions of helping someone in need, her intention wasn’t to start a war, or make people upset etc…that’s not her nature!!! At this point, whether you’re a Christian etc…Crohn’s can attack anyone regardless of your age, etc…I would like to believe that in the near future they will find a cure, for this miserable disease… Margie, please don’t go!!! We need you!!! You know how you can reach me, if you need to talk…don’t let this people get to you… For me, I can also count how many times, I’ve been in the hospital, than home and there’s an overnight bag ready with all the things I will need when I get to ER and what I will need to during my stay!!! For the people who want to cause trouble, hurt other people’s feelings, or cause even more stress, please I suggest to you STOP!!! it’s not worth it!!! Margie is a sweet person and a very good friend to have!!! Love Tania

Response:

- Hide quoted text — Show quoted text – I had no idea that one could recieve moneies for sending people their way. Newsgroups: alt.support.crohns-colitis Dear Ken:  Congratulations!  By the way, to anyone who uses or used Allsup at my reccommendation, ***please give them my name.*** I have been reccommending them ever since my approval and did not find out about the referral thing until the other day!  So, I would appreciate it if you guys would give my name, Marjorie Olige, if you do decide to use them.  They are the best!  I know this sounds cheesy, but ***I could use any monies I could get!*** Thanks.  And Ken I know you must be as happy as I was.  I did have to go through the hearing, but it wasn’t as bad as I was afraid it might be.  In fact, my case worker gave all the information to the judge, he then asked me a few questions and it was all over in less than a half an hour!  I was so thrilled to finally be approved!  My very first filing with SS was over 20 years ago when they told me to retrain, which I did and found I was able to go back to work.  In fact I was able to fulfill my dream of nursing at that time, so I guess they were right. But when I could no longer work under any circumstances, I finally went through Allsup, due to a TV commercial I saw, and they handled it all!  It took almost 2 years, but it sure was worth it!  I think they are wonderful!  Well, let me get off my soap box here and let you all get on about your business.  Ken, I wish you wellness. Love,  Margie CD Class of 67 UC Class of 96

Exactly what’s the purpose of all of this?  And why should any of us really get overly excited about posts from years ago?   Hugs, Love, Peace and Good Tidings to you all :) –Staci–

Response:

nobody had better be giving marge a hard time, or i will meet them on the street.  some of these trolls are in my kill file, i only have a few and these guys are it.  i don’t exactly know what they are up to but they had better leave marge alone! jeffy

– Hide quoted text — Show quoted text – I’m amazed that Perry seems to have enough time at work to read all the current posts as well as all the ones from 3 years ago — I want *his* job! Hey Sue — how about the ng charter again???? This is supposed to be a support group and I know that over the last 5 years, Margie has been a wonderful source of support for me! Perhaps others here need to remember that. Rebecca :-) Did you ever think she forgot with all the meds she is on and on the illness she has?  This is down right mean NA.  For the rest of you if you go to the link supplied start at the beginning of the thread so you get the whole picture of this thread.   I am very sad that people who need support are getting trashed.  Why?  Can you answer me this because I don’t understand. With all the meds and medical stuff I have gone through in the last three years I am happy when I remember the last time I ate or what it was.  I forget daily stuff never mind stuff back too the year 2000.  UM MOM Susan I had no idea that one could recieve moneies for sending people their way.  Newsgroups: alt.support.crohns-colitis Dear Ken:   Congratulations!  By the way, to anyone who uses or used Allsup at my reccommendation, ***please give them my name.***  I have been reccommending them ever since my approval and did not find out about the referral thing until the other day!  So, I would appreciate it if you guys would give my name, Marjorie Olige, if you do decide to use them.  They are the best!  I know this sounds cheesy, but  ***I could use any monies I could get!***  Thanks.  And Ken I know you must be as happy as I was.  I did have to go through the hearing, but it wasn’t as bad as I was afraid it might be.  In fact, my case worker gave all the information to the judge, he then asked me a few questions and it was all over in less than a half an hour!  I was so thrilled to finally be approved!  My very first filing with SS was over 20 years ago when they told me to retrain, which I did and found I was able to go back to work.  In fact I was able to fulfill my dream of nursing at that time, so I guess they were right. But when I could no longer work under any circumstances, I finally went through Allsup, due to a TV commercial I saw, and they handled it all!  It took almost 2 years, but it sure was worth it!  I think they are wonderful!  Well, let me get off my soap box here and let you all get on about your business.  Ken, I wish you wellness. Love,   Margie CD Class of 67 UC Class of 96 [original post:

http://groups.google.com/groups?q=marjorie+allsup+group:alt.support.c... olitis&hl=en&lr=&ie=UTF-8&selm=20000506191645.05274.00001242%40ng-cq1.aol.c o - Hide quoted text -- Show quoted text - m&rnum=1]

Response:

I’m amazed that Perry seems to have enough time at work to read all the current posts as well as all the ones from 3 years ago — I want *his* job! Hey Sue — how about the ng charter again???? This is supposed to be a support group and I know that over the last 5 years, Margie has been a wonderful source of support for me! Perhaps others here need to remember that. Rebecca :-)

– Hide quoted text — Show quoted text – Did you ever think she forgot with all the meds she is on and on the illness she has?  This is down right mean NA.  For the rest of you if you go to the link supplied start at the beginning of the thread so you get the whole picture of this thread.   I am very sad that people who need support are getting trashed.  Why?  Can you answer me this because I don’t understand. With all the meds and medical stuff I have gone through in the last three years I am happy when I remember the last time I ate or what it was.  I forget daily stuff never mind stuff back too the year 2000.  UM MOM Susan I had no idea that one could recieve moneies for sending people their way.  Newsgroups: alt.support.crohns-colitis Dear Ken:   Congratulations!  By the way, to anyone who uses or used Allsup at my reccommendation, ***please give them my name.***  I have been reccommending them ever since my approval and did not find out about the referral thing until the other day!  So, I would appreciate it if you guys would give my name, Marjorie Olige, if you do decide to use them.  They are the best!  I know this sounds cheesy, but  ***I could use any monies I could get!***  Thanks.  And Ken I know you must be as happy as I was.  I did have to go through the hearing, but it wasn’t as bad as I was afraid it might be.  In fact, my case worker gave all the information to the judge, he then asked me a few questions and it was all over in less than a half an hour!  I was so thrilled to finally be approved!  My very first filing with SS was over 20 years ago when they told me to retrain, which I did and found I was able to go back to work.  In fact I was able to fulfill my dream of nursing at that time, so I guess they were right. But when I could no longer work under any circumstances, I finally went through Allsup, due to a TV commercial I saw, and they handled it all!  It took almost 2 years, but it sure was worth it!  I think they are wonderful!  Well, let me get off my soap box here and let you all get on about your business.  Ken, I wish you wellness. Love,   Margie CD Class of 67 UC Class of 96 [original post:

http://groups.google.com/groups?q=marjorie+allsup+group:alt.support.c... olitis&hl=en&lr=&ie=UTF-8&selm=20000506191645.05274.00001242%40ng-cq1.aol.c o - Hide quoted text -- Show quoted text - m&rnum=1]

Response:

Did you ever think she forgot with all the meds she is on and on the illness she has?  This is down right mean NA.  For the rest of you if you go to the link supplied start at the beginning of the thread so you get the whole picture of this thread.   I am very sad that people who need support are getting trashed.  Why?  Can you answer me this because I don’t understand. With all the meds and medical stuff I have gone through in the last three years I am happy when I remember the last time I ate or what it was.  I forget daily stuff never mind stuff back too the year 2000.  UM MOM Susan

– Hide quoted text — Show quoted text – I had no idea that one could recieve moneies for sending people their way.  Newsgroups: alt.support.crohns-colitis Dear Ken:   Congratulations!  By the way, to anyone who uses or used Allsup at my reccommendation, ***please give them my name.***  I have been reccommending them ever since my approval and did not find out about the referral thing until the other day!  So, I would appreciate it if you guys would give my name, Marjorie Olige, if you do decide to use them.  They are the best!  I know this sounds cheesy, but  ***I could use any monies I could get!***  Thanks.  And Ken I know you must be as happy as I was.  I did have to go through the hearing, but it wasn’t as bad as I was afraid it might be.  In fact, my case worker gave all the information to the judge, he then asked me a few questions and it was all over in less than a half an hour!  I was so thrilled to finally be approved!  My very first filing with SS was over 20 years ago when they told me to retrain, which I did and found I was able to go back to work.  In fact I was able to fulfill my dream of nursing at that time, so I guess they were right. But when I could no longer work under any circumstances, I finally went through Allsup, due to a TV commercial I saw, and they handled it all!  It took almost 2 years, but it sure was worth it!  I think they are wonderful!  Well, let me get off my soap box here and let you all get on about your business.  Ken, I wish you wellness. Love,   Margie CD Class of 67 UC Class of 96 [original post:

http://groups.google.com/groups?q=marjorie+allsup+group:alt.support.c... olitis&hl=en&lr=&ie=UTF-8&selm=20000506191645.05274.00001242%40ng-cq1.aol.c o m&rnum=1]

Response:

To All I Promised This Number To:    This is the only reason I am posting right now.  I have promised some of you guys that I would get that number for you for the company that helped me.  I hope they can help you as well.  If it means anything to you, I get NOTHING, NOTHING, NOTHING for passing this number on

 Newsgroups: alt.support.crohns-colitis Dear Ken:  Congratulations!  By the way, to anyone who uses or used Allsup at my reccommendation, please give them my name.  I have been reccommending them ever since my approval and did not find out about ***the referral thing*** until the other day!  So, I would appreciate it if you guys would give my name, Marjorie Olige, if you do decide to use them.  They are the best!  I know this sounds cheesy, but ***I could use any monies I could get!***  Thanks.   [original post: http://groups.google.com/groups?q=marjorie+allsup+group:alt.support.c...]

Response:

I had no idea that one could recieve moneies for sending people their way.

 Newsgroups: alt.support.crohns-colitis Dear Ken:   Congratulations!  By the way, to anyone who uses or used Allsup at my reccommendation, ***please give them my name.***  I have been reccommending them ever since my approval and did not find out about the referral thing until the other day!  So, I would appreciate it if you guys would give my name, Marjorie Olige, if you do decide to use them.  They are the best!  I know this sounds cheesy, but  ***I could use any monies I could get!***  Thanks.  And Ken I know you must be as happy as I was.  I did have to go through the hearing, but it wasn’t as bad as I was afraid it might be.  In fact, my case worker gave all the information to the judge, he then asked me a few questions and it was all over in less than a half an hour!  I was so thrilled to finally be approved!  My very first filing with SS was over 20 years ago when they told me to retrain, which I did and found I was able to go back to work.  In fact I was able to fulfill my dream of nursing at that time, so I guess they were right. But when I could no longer work under any circumstances, I finally went through Allsup, due to a TV commercial I saw, and they handled it all!  It took almost 2 years, but it sure was worth it!  I think they are wonderful!  Well, let me get off my soap box here and let you all get on about your business.  Ken, I wish you wellness. Love,   Margie CD Class of 67 UC Class of 96 [original post: http://groups.google.com/groups?q=marjorie+allsup+group:alt.support.c...]

Response:

Navid if you would I would appreciate it if you would stop on Margie.  She is a friend I know and talk to other than the computer and as for your question, yes she will and she does for all of us even me who is not a Christian.  So please leave her alone.  She really needs this group and is feeling a little better but she is in the hospital more than she is at home and deals with some very serious problems of the disease.  Thank you for understanding.   She needs support not to be upset or chased away from the group.  Thanks again UM MOM Susan

– Hide quoted text — Show quoted text – " Navid, NA, anyone else, say what you will, I really don’t care." Margie. Margie, you should know by now, l alway’s do :o ) Margie, will you pray for my soul, even though l am not a Christian child? Navid

Response:

" Navid, NA, anyone else, say what you will, I really don’t care." Margie. Margie, you should know by now, l alway’s do :o ) Margie, will you pray for my soul, even though l am not a Christian child? Navid

Response:

Hi Margie, I’m sure there are many who really appreciate your help on this matter.  You were very kind and thoughtful to post the SSD information.  Thank you :) I am thrilled to hear you are doing so much better.  Continued success to you!   Hugs,  Linda – Hide quoted text — Show quoted text – Last I checked, they also had an informative website at www.allsupinc.com.  There are several people on the ng who have obtained SSD using their services Dear Sue:   I am so glad you put that in here.  I did check it and for what it means to anyone, until I just looked at it now, I had no idea that one could recieve moneies for sending people their way.  I apologize for that.  All I can say is, please feel free NOT to mention my name.  In fact, I would prefer it.  You see, at the time I used Allsup I don’t THINK they had this policy, but I did not pass the number on for that. So please, just call them but leave me out of it. Okay?  Thanks.  Navid, NA, anyone else, say what you will, I really don’t care. I must say I am glad to see they have that website now so you can do it all online.  All who would talk bad about me….have at it…I no longer care.   Margie CD Class of 67 UC Class of 96

Response:

Last I checked, they also had an informative website at www.allsupinc.com.  There are several people on the ng who have obtained SSD using their services

Dear Sue:   I am so glad you put that in here.  I did check it and for what it means to anyone, until I just looked at it now, I had no idea that one could recieve moneies for sending people their way.  I apologize for that.  All I can say is, please feel free NOT to mention my name.  In fact, I would prefer it.  You see, at the time I used Allsup I don’t THINK they had this policy, but I did not pass the number on for that. So please, just call them but leave me out of it. Okay?  Thanks.  Navid, NA, anyone else, say what you will, I really don’t care. I must say I am glad to see they have that website now so you can do it all online.  All who would talk bad about me….have at it…I no longer care.   Margie CD Class of 67 UC Class of 96

Response:

Last I checked, they also had an informative website at www.allsupinc.com.  There are several people on the ng who have obtained SSD using their services. – Hide quoted text — Show quoted text -To All I Promised This Number To:   This is the only reason I am posting right now.  I have promised some of you guys that I would get that number for you for the company that helped me.  I hope they can help you as well.  If it means anything to you, I get NOTHING, NOTHING, NOTHING for passing this number on except the good feeling that I may have helped someone.  So…anyway the name of the company is Allsup Inc and the number I have for them is 1-800-854-1418.  They are open from 8am to 5pm Central Time.  I wish you all well and I hope this helps.  Many of you are still on my prayer list.  Some of you I have come to dearly care about.  So stay well, and God bless.   Love,  Margie CD Class of 67 UC Class of 96

Response:

- Hide quoted text — Show quoted text – To All I Promised This Number To:    This is the only reason I am posting right now.  I have promised some of you guys that I would get that number for you for the company that helped me.  I hope they can help you as well.  If it means anything to you, I get NOTHING, NOTHING, NOTHING for passing this number on except the good feeling that I may have helped someone.  So…anyway the name of the company is Allsup Inc and the number I have for them is 1-800-854-1418.  They are open from 8am to 5pm Central Time.  I wish you all well and I hope this helps.  Many of you are still on my prayer list.  Some of you I have come to dearly care about.  So stay well, and God bless.   Love,   Margie CD Class of 67 UC Class of 96

hi i dont know what this number is and all ..i DO know that i got on ssd…when iwas turned down on the second try which is nothing more than the first one over again..and most are turned down..ss sent me a list of lawyers…in my area..i picked one..she was great..she went over my info first..before taking the case..and ironically my divorce lawyer came up with the best info of all..to keep a daily journal of symptoms and activities..she found THAT info in a law journal to do with disability hearings..it was specifically for ibd.. so i did ..and with the disability lawyer went to the hearing and 6 weeks later was on ssd..and also got back pay going back to when i first applied…2 years previously..the cost is always the same for the lawyers for disability..up to 25percent of the retroactive pay u get…it was well worth it..u get medicare automatically..parts a and b..and while i personally dont need them yet..its worth paying for them now..as i will have them later ..i only get 372 a month once medicare comes out..but…its better than nothing and pays for meds and stuff..and when i was going thru divorce and fighting to get anything..it saved me..so good luck… if anyone wants to know more about the journal and how to do it properly i can post that later.. love to all annie

Response:

To All I Promised This Number To:    This is the only reason I am posting right now.  I have promised some of you guys that I would get that number for you for the company that helped me.  I hope they can help you as well.  If it means anything to you, I get NOTHING, NOTHING, NOTHING for passing this number on except the good feeling that I may have helped someone.  So…anyway the name of the company is Allsup Inc and the number I have for them is 1-800-854-1418.  They are open from 8am to 5pm Central Time.  I wish you all well and I hope this helps.  Many of you are still on my prayer list.  Some of you I have come to dearly care about.  So stay well, and God bless.   Love,   Margie CD Class of 67 UC Class of 96

Response:

Mutants, Genes, Germs and Flames

Question:

Hi On, Sorry it took so incredibly long to get back to you.  I had a bad infection all summer which I finally got rid of by taking an antibiotic (penicillin) which I had a very bad reaction to and am still recovering from.  As I’ve got 2400 (!) posts to go before I catch up on my ng reading, I’m paying for being away for so long! In answer to your question, there are 2 types of ng – the "official" ones and the "alt" ones.  The alt ones are a lot easier to start. You type up a proposal and post in on relavant ngs for discussion. The relevant (sp?) ngs are this one and alt.config in this case. The proposal would be a basis for the ng charter which sets forth the purpose of the ng and what is and isn’t allowed.  People discuss it, and if enough people think its a good idea, someone on alt.config with system administator access will send out the newgroup control message and voila! a new newsgroup.  Note 2 additional things:  there are some strict naming conventions that have to be followed, and with an alt. group there might be some propagation problems if people weren’t really that interested in it, though I think this latter issue isn’t as much of a problem as it was before the explosive growth of the internet.  Alt.config will have a FAQ with more details about this. Hope this helps, – Hide quoted text — Show quoted text -Sue hi :) Can I ask for some advice from you? Someone made a joke about it in above post: "I guess someone snuck onto my computer and signed me up to alt.argue.crohns-colitis.   Allen" But seriously maybe its possible to start another ng for…. arguments and fights? (no kidin..) How does one start a ng ? Regards On Elpeleg Allen OK guys, things have gotten waaay out of hand.  I’ve never seen this much controversy about mutations outside of the XMen comic book.  Really immature stuff too like name calling and accusations of misspelling! Remember, a ng charter isn’t there just for the fun of it, most people’s ISPs ban violations of ng charters and will ban people from this ng or even throw them off their ISP’s if enough people complain about them.  I hate to have to remind people of this, but apparently all the really good reasons for not flaming on a support group aren’t registering this time around.  I’m not going to be around much thru Labor Day, so what say we all calm down before then so I don’t have to go thru the incredibly distasteful exercise of posting where to report ng abuse for each flamer. Once again, the ng charter: What is Alt.support.crohns-colitis? Alt.support.crohns-colitis was created in early 1994 as a forum where people suffering from ulcerative colitis, Crohn’s Disease, and irritable bowel syndrome can share their everyday struggles with these illnesses, as well as discuss medicines, treatments, surgery, diet, health care providers, related illnesses, and anything else anyone can think of that relates to these diseases.  In other words, this is the online equivalent of a support group, which means that no question is stupid and no condition embarrassing here.  It also means we’re all here to help each other out, so please be nice, be polite, and no flaming. Discussions of all types of medicine- conventional and alternative, Western and Eastern, your Aunt Harriet’s home remedies, whatever- are welcome here; however, any person discussing a potential remedy which he or she also sells must explicitly begin the "Subject" header of their post with the word "AD" or "ADVERTISEMENT" in all caps, regardless of whether or not they profit from such sales.  Spamming is expressly forbidden as violating the rules of netiquette as well as those of this newsgroup.  Finally, please keep in mind that no one knows what causes these illnesses, no one’s come up with a cure, and we need all the help we can get.

Response:

the "ignor" or kill file is too under used in here.  if ignorant people and people that degrade others are ignored, they end up going away. jeffy – Hide quoted text — Show quoted text – OK guys, things have gotten waaay out of hand.  I’ve never seen this much controversy about mutations outside of the XMen comic book.  Really immature stuff too like name calling and accusations of misspelling! Remember, a ng charter isn’t there just for the fun of it, most people’s ISPs ban violations of ng charters and will ban people from this ng or even throw them off their ISP’s if enough people complain about them.  I hate to have to remind people of this, but apparently all the really good reasons for not flaming on a support group aren’t registering this time around.  I’m not going to be around much thru Labor Day, so what say we all calm down before then so I don’t have to go thru the incredibly distasteful exercise of posting where to report ng abuse for each flamer. Once again, the ng charter: What is Alt.support.crohns-colitis? Alt.support.crohns-colitis was created in early 1994 as a forum where people suffering from ulcerative colitis, Crohn’s Disease, and irritable bowel syndrome can share their everyday struggles with these illnesses, as well as discuss medicines, treatments, surgery, diet, health care providers, related illnesses, and anything else anyone can think of that relates to these diseases.  In other words, this is the online equivalent of a support group, which means that no question is stupid and no condition embarrassing here.  It also means we’re all here to help each other out, so please be nice, be polite, and no flaming. Discussions of all types of medicine- conventional and alternative, Western and Eastern, your Aunt Harriet’s home remedies, whatever- are welcome here; however, any person discussing a potential remedy which he or she also sells must explicitly begin the "Subject" header of their post with the word "AD" or "ADVERTISEMENT" in all caps, regardless of whether or not they profit from such sales.  Spamming is expressly forbidden as violating the rules of netiquette as well as those of this newsgroup.  Finally, please keep in mind that no one knows what causes these illnesses, no one’s come up with a cure, and we need all the help we can get.

Response:

Sue hi :) Can I ask for some advice from you?  Someone made a joke about it in above post: "I guess someone snuck onto my computer and signed me up to alt.argue.crohns-colitis.   Allen" But seriously maybe its possible to start another ng for…. arguments and fights? (no kidin..) How does one start a ng ? Regards On Elpeleg Allen – Hide quoted text — Show quoted text – OK guys, things have gotten waaay out of hand.  I’ve never seen this much controversy about mutations outside of the XMen comic book.  Really immature stuff too like name calling and accusations of misspelling! Remember, a ng charter isn’t there just for the fun of it, most people’s ISPs ban violations of ng charters and will ban people from this ng or even throw them off their ISP’s if enough people complain about them.  I hate to have to remind people of this, but apparently all the really good reasons for not flaming on a support group aren’t registering this time around.  I’m not going to be around much thru Labor Day, so what say we all calm down before then so I don’t have to go thru the incredibly distasteful exercise of posting where to report ng abuse for each flamer. Once again, the ng charter: What is Alt.support.crohns-colitis? Alt.support.crohns-colitis was created in early 1994 as a forum where people suffering from ulcerative colitis, Crohn’s Disease, and irritable bowel syndrome can share their everyday struggles with these illnesses, as well as discuss medicines, treatments, surgery, diet, health care providers, related illnesses, and anything else anyone can think of that relates to these diseases.  In other words, this is the online equivalent of a support group, which means that no question is stupid and no condition embarrassing here.  It also means we’re all here to help each other out, so please be nice, be polite, and no flaming. Discussions of all types of medicine- conventional and alternative, Western and Eastern, your Aunt Harriet’s home remedies, whatever- are welcome here; however, any person discussing a potential remedy which he or she also sells must explicitly begin the "Subject" header of their post with the word "AD" or "ADVERTISEMENT" in all caps, regardless of whether or not they profit from such sales.  Spamming is expressly forbidden as violating the rules of netiquette as well as those of this newsgroup.  Finally, please keep in mind that no one knows what causes these illnesses, no one’s come up with a cure, and we need all the help we can get.

Response:

OK guys, things have gotten waaay out of hand.  I’ve never seen this much controversy about mutations outside of the XMen comic book.  Really immature stuff too like name calling and accusations of misspelling! Remember, a ng charter isn’t there just for the fun of it, most people’s ISPs ban violations of ng charters and will ban people from this ng or even throw them off their ISP’s if enough people complain about them.  I hate to have to remind people of this, but apparently all the really good reasons for not flaming on a support group aren’t registering this time around.  I’m not going to be around much thru Labor Day, so what say we all calm down before then so I don’t have to go thru the incredibly distasteful exercise of posting where to report ng abuse for each flamer. Once again, the ng charter: What is Alt.support.crohns-colitis? Alt.support.crohns-colitis was created in early 1994 as a forum where people suffering from ulcerative colitis, Crohn’s Disease, and irritable bowel syndrome can share their everyday struggles with these illnesses, as well as discuss medicines, treatments, surgery, diet, health care providers, related illnesses, and anything else anyone can think of that relates to these diseases.  In other words, this is the online equivalent of a support group, which means that no question is stupid and no condition embarrassing here.  It also means we’re all here to help each other out, so please be nice, be polite, and no flaming. Discussions of all types of medicine- conventional and alternative, Western and Eastern, your Aunt Harriet’s home remedies, whatever- are welcome here; however, any person discussing a potential remedy which he or she also sells must explicitly begin the "Subject" header of their post with the word "AD" or "ADVERTISEMENT" in all caps, regardless of whether or not they profit from such sales.  Spamming is expressly forbidden as violating the rules of netiquette as well as those of this newsgroup.  Finally, please keep in mind that no one knows what causes these illnesses, no one’s come up with a cure, and we need all the help we can get.

Response:

The important things in life.

Question:

Hi On, You seem like a very nice and very well informed (about IBD) person, but you’re missing a couple of things in this discussion because a)you’re a newbie to the ng and don’t know everyone’s background yet, and b)your English, while lightyears better than my command of any foreign language, isn’t quite at the level to grasp all the subtleties of some of the posts.  NA’s been around for months, he picks one person at a time to use as target practice and follows them around relentlessly trying to drive them off the ng.  Sometimes he uses blatant personal attacks, other times he’s more subtle and pretends to be solicitous.  The Turner/NA post you’re defending was, to anyone who’s been reading his posts for months, not an attempt to help Alan out but a thinly disguised attack. The most important rule on this ng is to always be nice, never flame. People come here for support and emotional succor, they need a refuge from the pain this illness is causing them in their lives.  Flaming, even in response to the flames of others, is against the ng charter. Did you notice the appearance and subsequent disappearance of Lisa Quinn on the thread about MAP?  She’s new, and the flames drove her off, and now she might miss advice which could really help her. I don’t know why Alan took Mr. Turner’s flamebait, he’s been very good about not doing so in the past, but we’re all human and slip up once in awhile.  You have shown yourself to be human too by not reading the ng charter in advance and refraining from flaming, not to mention not following standard Usenet protocol of reading a ng for awhile to learn about people like Alan, NA and Martin before posting replies.  No biggie, like I said, it’s obvious you’re an intelligent, nice guy who’s capable of engaging in debate without flaming or responding to flames, and as you continue to read the ng I’m sure you’ll figure out who’s who.  I’ll even bet that both you and Alan can debate each other respectfully- all you both have to do is not give Mr. Turner what he wants by letting him set the tone. Just in case you missed it before, here’s the ng charter: What is Alt.support.crohns-colitis? Alt.support.crohns-colitis was created in early 1994 as a forum where people suffering from ulcerative colitis, Crohn’s Disease, and irritable bowel syndrome can share their everyday struggles with these illnesses, as well as discuss medicines, treatments, surgery, diet, health care providers, related illnesses, and anything else anyone can think of that relates to these diseases.  In other words, this is the online equivalent of a support group, which means that no question is stupid and no condition embarrassing here.  It also means we’re all here to help each other out, so please be nice, be polite, and no flaming. Discussions of all types of medicine- conventional and alternative, Western and Eastern, your Aunt Harriet’s home remedies, whatever- are welcome here; however, any person discussing a potential remedy which he or she also sells must explicitly begin the "Subject" header of their post with the word "AD" or "ADVERTISEMENT" in all caps, regardless of whether or not they profit from such sales.  Spamming is expressly forbidden as violating the rules of netiquette as well as those of this newsgroup.  Finally, please keep in mind that no one knows what causes these illnesses, no one’s come up with a cure, and we need all the help we can get. – Hide quoted text — Show quoted text -Always look at the bright side of life…. As an unappointed advocate for NA if I may say ‘objection!..’  NA was merely trying to suggest that the material that Alan is coming with is very interesting , and should he place it in an organized form in a web site, it would win plenty of creditability and maybe more people would take the research results he comes with more seriously. (A constructive suggestion…). Sorry for sticking my nose… On Elpeleg By the way: I’m unclear why you have time to post multiple posts and responses here, but you say you don’t have time to update your web site. I think that was an uncalled for statement. I am not sure how much experience you have with website development but to put together a site that is well organized and easy to use takes a fair amount of time, to say nothing of updating it on a regular basis, while typing a response here can be done very quickly.

Response:

On, it’s all a question of credibility.  If that recent thread was all I had ever read of the ng I would feel as you feel.  In fact, that’s a big problem with flaming, people lose credibility doing it, and as a result I don’t understand why people who have serious arguments to make do it.  The thing is, as I said in the other post to you, Alan has built up a big bank of credibility on this ng over the years by remaining calm, reasonable and not flaming- he even toned down Mike considerably over MAP by arguing with him that MAP was *not* the be-all and end-all of CD treatment.  People here are giving him the benefit of the doubt because not all that credibility can be lost by one mistake, especially when that mistake is taking flamebait. OTOH, Mr. Turner has, by flaming, baiting, stooping to personal attacks when proven wrong by someone, and yes even using some of the fallacious debating techniques he derides in others, lost most of his credibility with this particular audience – which is a shame as he posts a lot of worthwhile material too. – Hide quoted text — Show quoted text – Your a strange one On. You’ll attack Alan Kennedy when he posts information on Crohn’s research and his view about where we are at with this disease. When Alans bonafides have been known to this group for several years. Hi John Science is not football :) Its not about being nice or not being nice… But if you are to put your self in a position of a judge and  give grades for who was the nicest one in the discussion…and you are to convince us that Alan is an innocent lamb…and everyone that disagrees with him is a bad woolf, I could only recommend you to go back to the discussion (MAP vs. genetics) from day one and read  it. I for one think that you are not looking at the things objectivly. But then, you’ll stick up for NA who in my view is a "loose canon" and I think thats being as nice as I can be regarding NA. I think it’s obvious that Alan’s got so much on his plate that to keep his website up to date is getting a bit ‘picky’ Again you are coming with the ‘who is the nicest one..’, I understand it… and fully respect and accept it, after all we are in some sort of support group. And people should be nice with eachother in a support group, now let me ask you something… how would you respond if I am to suggest that you are a confused, ignorant, inhuman, immature, anonymouse agitator? John you seem to have  a strong opinion of Alan being the nice guy… and NA the bad guy… Alan is the poor victim and NA is the victimizer… and you are fighting for saving the victim from their bad bad.. victimizer. You reckon it may be possible for you to try looking at things from a different angle? If Alan is to inform the world about his work, would you agree that this support group is actualy a drop in the oceane?  do you know how many IBD mailing lists exist out there? I found hundreds of them! some of them have thousands of members! But than again everything that NA says is wrong… because he is not nice. (by the way it doesnt cost anything today to run a complete website free of charge except few hours work, and i am certain that www.crohns.org would be happy to help Alan in starting such a site… or maybe you and the other fans could even contribute?). I just can’t work out where your coming from! Well since you have not asked I would answer :) in my culture a person that phrases another person as a ‘confused, ignorant, inhuman, immature, anonymouse agitator’ in a scientifical discussion.. is not taken seriously, but than again we all come from different places and cultures.. just as you suggested.  So maybe like you suggest its all a geographical problem and what one sees from here you can not see from there…  ;) Cheers, John H(I) Always look at the bright side of life…. As an unappointed advocate for NA if I may say ‘objection!..’  NA was merely trying to suggest that the material that Alan is coming with is very interesting , and should he place it in an organized form in a web site, it would win plenty of creditability and maybe more people would take the research results he comes with more seriously. (A constructive suggestion…). Sorry for sticking my nose… On Elpeleg By the way: I’m unclear why you have time to post multiple posts and responses here, but you say you don’t have time to update your web site. I think that was an uncalled for statement. I am not sure how much experience you have with website development but to put together a site that is well organized and easy to use takes a fair amount of time, to say nothing of updating it on a regular basis, while typing a response here can be done very quickly.

Response:

I personally think the comment was flame bait. . . . but, then, that is just my opinion. . . Rebecca <:-) foil hat on —-

– Hide quoted text — Show quoted text – By the way: I’m unclear why you have time to post multiple posts and responses here, but you say you don’t have time to update your web site. I think that was an uncalled for statement. I am not sure how much experience you have with website development but to put together a site that is well organized and easy to use takes a fair amount of time, to say nothing of updating it on a regular basis, while typing a response here can be done very quickly.

Response:

Epeleg and NA are cut from the same cloth i believe…..If someone has something to say that doesn’t coincide to there way of thinking they will try to bash it…   eg. I’m not for immune suppression…. I believe in building the Immune system up…we were given an immune system to protect us from diseases and whoever is responsible for it i believe he knew what he was doing. That fly’s right into the face of what NA seems to believe in so he tries to bash it whenever he can, even though most people who do good usually strengthen there immune ssystem by diet, nutrition, and exercise when fighting chronic diseases. Epeleg doesn’t believe in Companies being fair to there workers so he calls USANA a scam.  He much rather see the people on top making the money as compared to the people who do the work.  He likes the Corporate infrastucture where the CEo’s make more in a year then the employees will see in a lifetime! USANA’s CEO and founder Dr. Myron Wentz receives no wages or bonuses from USANA and yet he still has the audacity to call it a scam. But you won’t see him back up what he says…At least I haven’t. Ken.W  7 Years Med Free! Proud member of the USANA Family

– Hide quoted text — Show quoted text – Your a strange one On. You’ll attack Alan Kennedy when he posts information on Crohn’s research and his view about where we are at with this disease. When Alans bonafides have been known to this group for several years. But then, you’ll stick up for NA who in my view is a "loose canon" and I think thats being as nice as I can be regarding NA. I think it’s obvious that Alan’s got so much on his plate that to keep his website up to date is getting a bit ‘picky’ I just can’t work out where your coming from! Cheers, John H(I) Always look at the bright side of life…. As an unappointed advocate for NA if I may say ‘objection!..’  NA was merely trying to suggest that the material that Alan is coming with is very interesting , and should he place it in an organized form in a web site, it would win plenty of creditability and maybe more people would take the research results he comes with more seriously. (A constructive suggestion…). Sorry for sticking my nose… On Elpeleg By the way: I’m unclear why you have time to post multiple posts and responses here, but you say you don’t have time to update your web site. I think that was an uncalled for statement. I am not sure how much experience you have with website development but to put together a site that is well organized and easy to use takes a fair amount of time, to say nothing of updating it on a regular basis, while typing a response here can be done very quickly.

Response:

Thanks for the post, Alan. First, please know I am thinking about your mom — losing a pet is never easy, and especially one who has so brought much comfort for so many years. What a good son you are to spend some time with her. I’m sure she appreciated it. Second, I have always enjoyed your posts and contributions to the ng. You were one of the first posters I remember when I first arrived here and over the years you have given me much to think about. While I have to admit I don’t always understand all of what you post (ok, MOST of what you post <G) I appreciate your complete commitment to finding answers to our disease. Please, please, please continue to post both the technical and personal information you have to share. Many of us here (most, actually) applaud you for your tireless work! As far as the negative energy — yes, it seems to surface every once in awhile around here. The best thing to do is ignore it. Just give your foil hat a tug, so it fits nice and tight and send out a few (((((((hugs))))))) to the posters who need them, and we’ll make sure that negative energy goes away fast!  I always figure people who pick on others is really a sign of their own unhappiness and low self esteem — and that is very sad. I read a couple other ng — and we are quite lucky we don’t have more negative/hurtful people. Thanks again  — and again, my thoughts and prayers for your mom. Hope you are feeling well. Rebecca :-)

– Hide quoted text — Show quoted text – Hi All, I’ve been away for a few days, staying out in my mothers. Her 15 1/2 year old dog passed away on Monday. She was quite upset about it, because she’s had the dog since her husband (my father) passed away 15 years ago. So I went out to keep her company. On Monday, as I spent an hour burying the beloved pooch in the back garden, I had much time to reflect on life and death, happiness and unhappiness, healthiness and suffering. It was a sad time. The conclusion that I came to was the one that I always come to: That we are all lucky to have our time in this world. Some of us are less lucky, in that health problems sometimes prevent us from realising the fullness of our potential. It is particularly sad when this affects children. I realised then that I have an important job to do, and that it is not yet finished. I also realised if I’m going to achieve anything, then I need my full emotional strength, so as to be able to handle the inevitable accusations of self-interest that always arise. When I started out my long journey five years ago, I knew that I would come under sustained personal criticism, suspicion and attack. There are just too many vested interests involved for that not to be the case. It is ironic that by far the most vitriolic and anti-personal attacks originate from within the very group that I started out to help. Ironic, but not surprising, however, since the destructive nature of Crohn’s Disease forces us all to construct world pictures, sometimes based on assumptions and hopes, that permits us to live life without going insane. If someone challenges those assumptions and hopes, then it is only to be expected that we will sometimes strike out against that someone with vigorous force. I am fully aware that this is a support newsgroup. People come to this newsgroup for "Discussions of all types of medicine — conventional and alternative, Western and Eastern, your Aunt Harriet’s home remedies, whatever — are welcome here;", according to the Newsgroup charter. http://ascc.healingwell.com/info/charter.html I make posts into the newsgroup about MAP and Crohn’s Disease related news because I believe that people want to hear about them. Sometimes these announcements result in extensive debates, in which I endeavour to always support my point of view with research and facts. Many times, these debates get personal, and though I dislike being personally attacked for my point of view, I endeavour to not let it get under my skin, and to reply in a sensible and mature fashion. But some of these discussions of the previous two weeks have resulted in heated emotional discussions, with plenty of negative emotional energy flying around. Although I don’t feel responsible for infusing this negative emotional energy into the group, I still don’t want it to happen. I don’t want this newsgroup to be polluted with negative emotion, not only because it’s against the newsgroup charter, but it’s a waste of my and others valuable emotional energy. So, the question I put to the newsgroup is this: Do people in this newsgroup want me to post information bulletins about the latest of Crohn’s Disease and MAP research? If people don’t want to hear about it, then I won’t post it any more. Sincerely, Alan Kennedy.

Response:

Your a strange one On. You’ll attack Alan Kennedy when he posts information on Crohn’s research and his view about where we are at with this disease. When Alans bonafides have been known to this group for several years.

Hi John Science is not football :) Its not about being nice or not being nice… But if you are to put your self in a position of a judge and  give grades for who was the nicest one in the discussion…and you are to convince us that Alan is an innocent lamb…and everyone that disagrees with him is a bad woolf, I could only recommend you to go back to the discussion (MAP vs. genetics) from day one and read  it. I for one think that you are not looking at the things objectivly. But then, you’ll stick up for NA who in my view is a "loose canon" and I think thats being as nice as I can be regarding NA. I think it’s obvious that Alan’s got so much on his plate that to keep his website up to date is getting a bit ‘picky’

Again you are coming with the ‘who is the nicest one..’, I understand it… and fully respect and accept it, after all we are in some sort of support group. And people should be nice with eachother in a support group, now let me ask you something… how would you respond if I am to suggest that you are a confused, ignorant, inhuman, immature, anonymouse agitator? John you seem to have  a strong opinion of Alan being the nice guy… and NA the bad guy… Alan is the poor victim and NA is the victimizer… and you are fighting for saving the victim from their bad bad.. victimizer. You reckon it may be possible for you to try looking at things from a different angle? If Alan is to inform the world about his work, would you agree that this support group is actualy a drop in the oceane?  do you know how many IBD mailing lists exist out there? I found hundreds of them! some of them have thousands of members! But than again everything that NA says is wrong… because he is not nice. (by the way it doesnt cost anything today to run a complete website free of charge except few hours work, and i am certain that www.crohns.org would be happy to help Alan in starting such a site… or maybe you and the other fans could even contribute?). I just can’t work out where your coming from!

Well since you have not asked I would answer :) in my culture a person that phrases another person as a ‘confused, ignorant, inhuman, immature, anonymouse agitator’ in a scientifical discussion.. is not taken seriously, but than again we all come from different places and cultures.. just as you suggested.  So maybe like you suggest its all a geographical problem and what one sees from here you can not see from there…  ;) – Hide quoted text — Show quoted text – Cheers, John H(I) Always look at the bright side of life…. As an unappointed advocate for NA if I may say ‘objection!..’  NA was merely trying to suggest that the material that Alan is coming with is very interesting , and should he place it in an organized form in a web site, it would win plenty of creditability and maybe more people would take the research results he comes with more seriously. (A constructive suggestion…). Sorry for sticking my nose… On Elpeleg By the way: I’m unclear why you have time to post multiple posts and responses here, but you say you don’t have time to update your web site. I think that was an uncalled for statement. I am not sure how much experience you have with website development but to put together a site that is well organized and easy to use takes a fair amount of time, to say nothing of updating it on a regular basis, while typing a response here can be done very quickly.

Response:

Who are you talking to?  UM MOM Susan

– Hide quoted text — Show quoted text – PPS: I don’t feel responsible for infusing this negative emotional energy into the group Again, I urge you to take a more honest look at yourself.

Response:

Of course we do Alan.  I know you don’t visit the ng on a regular basis, so I doubt you know this, but Mr. Turner aka NA for months has been picking out one target at a time here and trying to drive him/her off with a patented mix of valid research info, sophistry and flames.  I believe the number of people who have completely screened out his messages actually exceeds the number of people who have screened out Ironman Tom the Watchman(who, interestingly since he learned to follow the ng charter and not flame appears to get more respect than Mr. Turner here).  You need to either filter him out like so many others do, complain about him to the Smithsonian Air and Space Mag along with copies of his flames, or do what you used to do in the past, what Ken W. has done so well even with NA, and that’s debate him without stooping to his level and flaming back.

Response:

Your a strange one On. You’ll attack Alan Kennedy when he posts information on Crohn’s research and his view about where we are at with this disease. When Alans bonafides have been known to this group for several years. But then, you’ll stick up for NA who in my view is a "loose canon" and I think thats being as nice as I can be regarding NA. I think it’s obvious that Alan’s got so much on his plate that to keep his website up to date is getting a bit ‘picky’ I just can’t work out where your coming from! Cheers, John H(I)

– Hide quoted text — Show quoted text – Always look at the bright side of life…. As an unappointed advocate for NA if I may say ‘objection!..’  NA was merely trying to suggest that the material that Alan is coming with is very interesting , and should he place it in an organized form in a web site, it would win plenty of creditability and maybe more people would take the research results he comes with more seriously. (A constructive suggestion…). Sorry for sticking my nose… On Elpeleg By the way: I’m unclear why you have time to post multiple posts and responses here, but you say you don’t have time to update your web site. I think that was an uncalled for statement. I am not sure how much experience you have with website development but to put together a site that is well organized and easy to use takes a fair amount of time, to say nothing of updating it on a regular basis, while typing a response here can be done very quickly.

Response:

hi alan, to be truthful, i really don’t know.  personally, i don’t read most of the map posts, i consider them about as speculative as any other "theory" going today on the "cause" of cd.  i don’t see the cause of cd coming around any too soon.  we don’t really even know how to treat the damn thing.  i think the majoity of us here would agree that of the treatments we have had or are on, it ain’t work’in.  some of us have been lucky enough to sweat it out long enough to finally fall into some form of treatment that helps, in varing degrees.  so, don’t take this as a yes or no, i really don’t know…i just don’t see enough evidence building up to prove any theory anytime soon. Jeffy

– Hide quoted text — Show quoted text – Hi All, I’ve been away for a few days, staying out in my mothers. Her 15 1/2 year old dog passed away on Monday. She was quite upset about it, because she’s had the dog since her husband (my father) passed away 15 years ago. So I went out to keep her company. On Monday, as I spent an hour burying the beloved pooch in the back garden, I had much time to reflect on life and death, happiness and unhappiness, healthiness and suffering. It was a sad time. The conclusion that I came to was the one that I always come to: That we are all lucky to have our time in this world. Some of us are less lucky, in that health problems sometimes prevent us from realising the fullness of our potential. It is particularly sad when this affects children. I realised then that I have an important job to do, and that it is not yet finished. I also realised if I’m going to achieve anything, then I need my full emotional strength, so as to be able to handle the inevitable accusations of self-interest that always arise. When I started out my long journey five years ago, I knew that I would come under sustained personal criticism, suspicion and attack. There are just too many vested interests involved for that not to be the case. It is ironic that by far the most vitriolic and anti-personal attacks originate from within the very group that I started out to help. Ironic, but not surprising, however, since the destructive nature of Crohn’s Disease forces us all to construct world pictures, sometimes based on assumptions and hopes, that permits us to live life without going insane. If someone challenges those assumptions and hopes, then it is only to be expected that we will sometimes strike out against that someone with vigorous force. I am fully aware that this is a support newsgroup. People come to this newsgroup for "Discussions of all types of medicine — conventional and alternative, Western and Eastern, your Aunt Harriet’s home remedies, whatever — are welcome here;", according to the Newsgroup charter. http://ascc.healingwell.com/info/charter.html I make posts into the newsgroup about MAP and Crohn’s Disease related news because I believe that people want to hear about them. Sometimes these announcements result in extensive debates, in which I endeavour to always support my point of view with research and facts. Many times, these debates get personal, and though I dislike being personally attacked for my point of view, I endeavour to not let it get under my skin, and to reply in a sensible and mature fashion. But some of these discussions of the previous two weeks have resulted in heated emotional discussions, with plenty of negative emotional energy flying around. Although I don’t feel responsible for infusing this negative emotional energy into the group, I still don’t want it to happen. I don’t want this newsgroup to be polluted with negative emotion, not only because it’s against the newsgroup charter, but it’s a waste of my and others valuable emotional energy. So, the question I put to the newsgroup is this: Do people in this newsgroup want me to post information bulletins about the latest of Crohn’s Disease and MAP research? If people don’t want to hear about it, then I won’t post it any more. Sincerely, Alan Kennedy.

Response:

PPS: I don’t feel responsible for infusing this negative emotional energy into the group

Again, I urge you to take a more honest look at yourself.

Response:

Always look at the bright side of life…. As an unappointed advocate for NA if I may say ‘objection!..’  NA was merely trying to suggest that the material that Alan is coming with is very interesting , and should he place it in an organized form in a web site, it would win plenty of creditability and maybe more people would take the research results he comes with more seriously. (A constructive suggestion…). Sorry for sticking my nose… On Elpeleg

– Hide quoted text — Show quoted text – By the way: I’m unclear why you have time to post multiple posts and responses here, but you say you don’t have time to update your web site. I think that was an uncalled for statement. I am not sure how much experience you have with website development but to put together a site that is well organized and easy to use takes a fair amount of time, to say nothing of updating it on a regular basis, while typing a response here can be done very quickly.

Response:

PS: some of these discussions of the previous two weeks have resulted in heated emotional discussions,

The essential nature of a newsgroup is interaction. People will always respond to your posts. You seem upset and shaken that people challenge your assertions, and post evidence that contradicts your posts, or point out errors you’ve made. If these challenges upset you so much, why not just post your MAP material on your own Website and be done with it? That way you won’t have to put up with disagreements and contradictory assertions. Every so often, you could post a simple statement on this newsgroup saying: "Please come to www.[whatever] and check out my latest MAP information." By the way: I’m unclear why you have time to post multiple posts and responses here, but you say you don’t have time to update your web site.

Response:

By the way: I’m unclear why you have time to post multiple posts and responses here, but you say you don’t have time to update your web site.

I think that was an uncalled for statement. I am not sure how much experience you have with website development but to put together a site that is well organized and easy to use takes a fair amount of time, to say nothing of updating it on a regular basis, while typing a response here can be done very quickly.

Response:

I don’t know if it’s just me but your link doesn’t work.  UM MOM Susan

– Hide quoted text — Show quoted text – PS: some of these discussions of the previous two weeks have resulted in heated emotional discussions, The essential nature of a newsgroup is interaction. People will always respond to your posts. You seem upset and shaken that people challenge your assertions, and post evidence that contradicts your posts, or point out errors you’ve made. If these challenges upset you so much, why not just post your MAP material on your own Website and be done with it? That way you won’t have to put up with disagreements and contradictory assertions. Every so often, you could post a simple statement on this newsgroup saying: "Please come to www.[whatever] and check out my latest MAP information." By the way: I’m unclear why you have time to post multiple posts and responses here, but you say you don’t have time to update your web site.

Response:

hi—please continue the posts–also–wouldn’t it be nice if similar sentiments were sent by some of the "combatants?" mel

Response:

Do people in this newsgroup want me to post information bulletins about the latest of Crohn’s Disease and MAP research?

Only if you stop relentlessly pitting MAP research against research into other avenues of IBD research, such as therapies based on immune suppression or cytokine regulation, for example. Realize that many people here are, in fact, getting relief through all sorts of non-RMAT therapies–and respect that. Enough with the "RMAT good!/conventional medicine bad!" crap. It’s tedious, and it turns people off. You only lose credibility when you indulge in your constant dark mutterings about the evils of conventional medicine, pharmaceutical development, epidemiology, etc., and your implicit claims only you and a few of your fellow MAP advocates are enlightened enough to see through the quagmire of corruption to The Truth. Frankly, the difference between your culture and ours is that ours is already exhausted by such conspiracy theories. Please also be honest with yourself, and realize that all your "I was only trying to help!" protestations have a strong whiff of self-pity to them. Not to mention self-beatification.

Response:

Your posts, reports, and other information you post are certainly of interest to me and I hope you keep posting them. Whether all, some or none of Crohns is caused by MAP is still to be determined, but I am happy there is research into more then one cause. The more research the better, and more likely finding a cause and then cure.

– Hide quoted text — Show quoted text – Hi All, I’ve been away for a few days, staying out in my mothers. Her 15 1/2 year old dog passed away on Monday. She was quite upset about it, because she’s had the dog since her husband (my father) passed away 15 years ago. So I went out to keep her company. On Monday, as I spent an hour burying the beloved pooch in the back garden, I had much time to reflect on life and death, happiness and unhappiness, healthiness and suffering. It was a sad time. The conclusion that I came to was the one that I always come to: That we are all lucky to have our time in this world. Some of us are less lucky, in that health problems sometimes prevent us from realising the fullness of our potential. It is particularly sad when this affects children. I realised then that I have an important job to do, and that it is not yet finished. I also realised if I’m going to achieve anything, then I need my full emotional strength, so as to be able to handle the inevitable accusations of self-interest that always arise. When I started out my long journey five years ago, I knew that I would come under sustained personal criticism, suspicion and attack. There are just too many vested interests involved for that not to be the case. It is ironic that by far the most vitriolic and anti-personal attacks originate from within the very group that I started out to help. Ironic, but not surprising, however, since the destructive nature of Crohn’s Disease forces us all to construct world pictures, sometimes based on assumptions and hopes, that permits us to live life without going insane. If someone challenges those assumptions and hopes, then it is only to be expected that we will sometimes strike out against that someone with vigorous force. I am fully aware that this is a support newsgroup. People come to this newsgroup for "Discussions of all types of medicine — conventional and alternative, Western and Eastern, your Aunt Harriet’s home remedies, whatever — are welcome here;", according to the Newsgroup charter. http://ascc.healingwell.com/info/charter.html I make posts into the newsgroup about MAP and Crohn’s Disease related news because I believe that people want to hear about them. Sometimes these announcements result in extensive debates, in which I endeavour to always support my point of view with research and facts. Many times, these debates get personal, and though I dislike being personally attacked for my point of view, I endeavour to not let it get under my skin, and to reply in a sensible and mature fashion. But some of these discussions of the previous two weeks have resulted in heated emotional discussions, with plenty of negative emotional energy flying around. Although I don’t feel responsible for infusing this negative emotional energy into the group, I still don’t want it to happen. I don’t want this newsgroup to be polluted with negative emotion, not only because it’s against the newsgroup charter, but it’s a waste of my and others valuable emotional energy. So, the question I put to the newsgroup is this: Do people in this newsgroup want me to post information bulletins about the latest of Crohn’s Disease and MAP research? If people don’t want to hear about it, then I won’t post it any more. Sincerely, Alan Kennedy.

Response:

I want to hear about every…EVERY…report relating to Crohn’s. The theory I have is that if WE can just live long enought they WILL find a way to fix all of our problems. Thanks

– Hide quoted text — Show quoted text – Hi All, I’ve been away for a few days, staying out in my mothers. Her 15 1/2 year old dog passed away on Monday. She was quite upset about it, because she’s had the dog since her husband (my father) passed away 15 years ago. So I went out to keep her company. On Monday, as I spent an hour burying the beloved pooch in the back garden, I had much time to reflect on life and death, happiness and unhappiness, healthiness and suffering. It was a sad time. The conclusion that I came to was the one that I always come to: That we are all lucky to have our time in this world. Some of us are less lucky, in that health problems sometimes prevent us from realising the fullness of our potential. It is particularly sad when this affects children. I realised then that I have an important job to do, and that it is not yet finished. I also realised if I’m going to achieve anything, then I need my full emotional strength, so as to be able to handle the inevitable accusations of self-interest that always arise. When I started out my long journey five years ago, I knew that I would come under sustained personal criticism, suspicion and attack. There are just too many vested interests involved for that not to be the case. It is ironic that by far the most vitriolic and anti-personal attacks originate from within the very group that I started out to help. Ironic, but not surprising, however, since the destructive nature of Crohn’s Disease forces us all to construct world pictures, sometimes based on assumptions and hopes, that permits us to live life without going insane. If someone challenges those assumptions and hopes, then it is only to be expected that we will sometimes strike out against that someone with vigorous force. I am fully aware that this is a support newsgroup. People come to this newsgroup for "Discussions of all types of medicine — conventional and alternative, Western and Eastern, your Aunt Harriet’s home remedies, whatever — are welcome here;", according to the Newsgroup charter. http://ascc.healingwell.com/info/charter.html I make posts into the newsgroup about MAP and Crohn’s Disease related news because I believe that people want to hear about them. Sometimes these announcements result in extensive debates, in which I endeavour to always support my point of view with research and facts. Many times, these debates get personal, and though I dislike being personally attacked for my point of view, I endeavour to not let it get under my skin, and to reply in a sensible and mature fashion. But some of these discussions of the previous two weeks have resulted in heated emotional discussions, with plenty of negative emotional energy flying around. Although I don’t feel responsible for infusing this negative emotional energy into the group, I still don’t want it to happen. I don’t want this newsgroup to be polluted with negative emotion, not only because it’s against the newsgroup charter, but it’s a waste of my and others valuable emotional energy. So, the question I put to the newsgroup is this: Do people in this newsgroup want me to post information bulletins about the latest of Crohn’s Disease and MAP research? If people don’t want to hear about it, then I won’t post it any more. Sincerely, Alan Kennedy.

Response:

I want to hear it. But let it be known that if I feel very strongly I will post a response. I have not and will try to never get personal. We are all on the same side here. Debs – Hide quoted text — Show quoted text – Hi All, I’ve been away for a few days, staying out in my mothers. Her 15 1/2 year old dog passed away on Monday. She was quite upset about it, because she’s had the dog since her husband (my father) passed away 15 years ago. So I went out to keep her company. On Monday, as I spent an hour burying the beloved pooch in the back garden, I had much time to reflect on life and death, happiness and unhappiness, healthiness and suffering. It was a sad time. The conclusion that I came to was the one that I always come to: That we are all lucky to have our time in this world. Some of us are less lucky, in that health problems sometimes prevent us from realising the fullness of our potential. It is particularly sad when this affects children. I realised then that I have an important job to do, and that it is not yet finished. I also realised if I’m going to achieve anything, then I need my full emotional strength, so as to be able to handle the inevitable accusations of self-interest that always arise. When I started out my long journey five years ago, I knew that I would come under sustained personal criticism, suspicion and attack. There are just too many vested interests involved for that not to be the case. It is ironic that by far the most vitriolic and anti-personal attacks originate from within the very group that I started out to help. Ironic, but not surprising, however, since the destructive nature of Crohn’s Disease forces us all to construct world pictures, sometimes based on assumptions and hopes, that permits us to live life without going insane. If someone challenges those assumptions and hopes, then it is only to be expected that we will sometimes strike out against that someone with vigorous force. I am fully aware that this is a support newsgroup. People come to this newsgroup for "Discussions of all types of medicine — conventional and alternative, Western and Eastern, your Aunt Harriet’s home remedies, whatever — are welcome here;", according to the Newsgroup charter. http://ascc.healingwell.com/info/charter.html I make posts into the newsgroup about MAP and Crohn’s Disease related news because I believe that people want to hear about them. Sometimes these announcements result in extensive debates, in which I endeavour to always support my point of view with research and facts. Many times, these debates get personal, and though I dislike being personally attacked for my point of view, I endeavour to not let it get under my skin, and to reply in a sensible and mature fashion. But some of these discussions of the previous two weeks have resulted in heated emotional discussions, with plenty of negative emotional energy flying around. Although I don’t feel responsible for infusing this negative emotional energy into the group, I still don’t want it to happen. I don’t want this newsgroup to be polluted with negative emotion, not only because it’s against the newsgroup charter, but it’s a waste of my and others valuable emotional energy. So, the question I put to the newsgroup is this: Do people in this newsgroup want me to post information bulletins about the latest of Crohn’s Disease and MAP research? If people don’t want to hear about it, then I won’t post it any more. Sincerely, Alan Kennedy.

Response:

Do people in this newsgroup want me to post information bulletins about the latest of Crohn’s Disease and MAP research?

Yes, please continue to post. I am one who is skeptical that MAP is the "cause" of CD, although I believe it may well be one of many different triggers of CD in susceptible people. But I’m willing to reexamine my beliefs in the light of new scientific data. Wayne Marsh          Minneapolis, Minnesota, USA

Response:

Alan please forward my sincere sympathy to your mother for losing her close friend. Concerning the issue of your writing here, I am a new user here and regardless of that I would like to refer to an answer I wrote to Chancy when she asked everyone here to help expelling Tom Hennessey from the list (enclosed bellow). I have no problem whatever with you ‘posting information bulletins about the latest of Crohn’s Disease and MAP research’, but should I come with critic and/or doubt concerning this information and will have to face baseless personal insults in return I would certainly have problems taking the information seriously. Regards On Elpeleg Chancy hi As long as Tom Hennessey doesn’t pretend to ‘have any of the diseases for which these groups have been set up to support, he does he care for anyone with them nor have any family with them. He has no recognised medical expertise and supports his thesis with glib quotations from NIH Medline and other sources which he dimly understands.’ I see no reason to

ban him, if he wants to argue for a certain treatment he better be good and better come with clinical trial documentation as well as references to articles in serious magazines. From what I can see he hasn’t done so yet. Reading his stuff here is harmless, but banning him may harm the list. Not just freedom of speech, but most important freedom of expression and discussion of any type of therapy. Regards On Elpeleg

– Hide quoted text — Show quoted text – Hi All, I’ve been away for a few days, staying out in my mothers. Her 15 1/2 year old dog passed away on Monday. She was quite upset about it, because she’s had the dog since her husband (my father) passed away 15 years ago. So I went out to keep her company. On Monday, as I spent an hour burying the beloved pooch in the back garden, I had much time to reflect on life and death, happiness and unhappiness, healthiness and suffering. It was a sad time. The conclusion that I came to was the one that I always come to: That we are all lucky to have our time in this world. Some of us are less lucky, in that health problems sometimes prevent us from realising the fullness of our potential. It is particularly sad when this affects children. I realised then that I have an important job to do, and that it is not yet finished. I also realised if I’m going to achieve anything, then I need my full emotional strength, so as to be able to handle the inevitable accusations of self-interest that always arise. When I started out my long journey five years ago, I knew that I would come under sustained personal criticism, suspicion and attack. There are just too many vested interests involved for that not to be the case. It is ironic that by far the most vitriolic and anti-personal attacks originate from within the very group that I started out to help. Ironic, but not surprising, however, since the destructive nature of Crohn’s Disease forces us all to construct world pictures, sometimes based on assumptions and hopes, that permits us to live life without going insane. If someone challenges those assumptions and hopes, then it is only to be expected that we will sometimes strike out against that someone with vigorous force. I am fully aware that this is a support newsgroup. People come to this newsgroup for "Discussions of all types of medicine — conventional and alternative, Western and Eastern, your Aunt Harriet’s home remedies, whatever — are welcome here;", according to the Newsgroup charter. http://ascc.healingwell.com/info/charter.html I make posts into the newsgroup about MAP and Crohn’s Disease related news because I believe that people want to hear about them. Sometimes these announcements result in extensive debates, in which I endeavour to always support my point of view with research and facts. Many times, these debates get personal, and though I dislike being personally attacked for my point of view, I endeavour to not let it get under my skin, and to reply in a sensible and mature fashion. But some of these discussions of the previous two weeks have resulted in heated emotional discussions, with plenty of negative emotional energy flying around. Although I don’t feel responsible for infusing this negative emotional energy into the group, I still don’t want it to happen. I don’t want this newsgroup to be polluted with negative emotion, not only because it’s against the newsgroup charter, but it’s a waste of my and others valuable emotional energy. So, the question I put to the newsgroup is this: Do people in this newsgroup want me to post information bulletins about the latest of Crohn’s Disease and MAP research? If people don’t want to hear about it, then I won’t post it any more. Sincerely, Alan Kennedy.

Response:

Yes, Definitly keep on posting….  It’s all good! I’ve gone through my share of doubts…don’t let the NA ’s and the Flippers of the world turn you away from what you believe in. It’s pretty hard to refute good science…. and when they do they just make themselves look bad…eg. take NA and me as an example. He blasts falsehoods about USANA and I blast him right back with the truth and it doesn’t take one long to see what kind of a person he is. Ken.W  7 Years Med Free!

– Hide quoted text — Show quoted text – Hi All, I’ve been away for a few days, staying out in my mothers. Her 15 1/2 year old dog passed away on Monday. She was quite upset about it, because she’s had the dog since her husband (my father) passed away 15 years ago. So I went out to keep her company. On Monday, as I spent an hour burying the beloved pooch in the back garden, I had much time to reflect on life and death, happiness and unhappiness, healthiness and suffering. It was a sad time. The conclusion that I came to was the one that I always come to: That we are all lucky to have our time in this world. Some of us are less lucky, in that health problems sometimes prevent us from realising the fullness of our potential. It is particularly sad when this affects children. I realised then that I have an important job to do, and that it is not yet finished. I also realised if I’m going to achieve anything, then I need my full emotional strength, so as to be able to handle the inevitable accusations of self-interest that always arise. When I started out my long journey five years ago, I knew that I would come under sustained personal criticism, suspicion and attack. There are just too many vested interests involved for that not to be the case. It is ironic that by far the most vitriolic and anti-personal attacks originate from within the very group that I started out to help. Ironic, but not surprising, however, since the destructive nature of Crohn’s Disease forces us all to construct world pictures, sometimes based on assumptions and hopes, that permits us to live life without going insane. If someone challenges those assumptions and hopes, then it is only to be expected that we will sometimes strike out against that someone with vigorous force. I am fully aware that this is a support newsgroup. People come to this newsgroup for "Discussions of all types of medicine — conventional and alternative, Western and Eastern, your Aunt Harriet’s home remedies, whatever — are welcome here;", according to the Newsgroup charter. http://ascc.healingwell.com/info/charter.html I make posts into the newsgroup about MAP and Crohn’s Disease related news because I believe that people want to hear about them. Sometimes these announcements result in extensive debates, in which I endeavour to always support my point of view with research and facts. Many times, these debates get personal, and though I dislike being personally attacked for my point of view, I endeavour to not let it get under my skin, and to reply in a sensible and mature fashion. But some of these discussions of the previous two weeks have resulted in heated emotional discussions, with plenty of negative emotional energy flying around. Although I don’t feel responsible for infusing this negative emotional energy into the group, I still don’t want it to happen. I don’t want this newsgroup to be polluted with negative emotion, not only because it’s against the newsgroup charter, but it’s a waste of my and others valuable emotional energy. So, the question I put to the newsgroup is this: Do people in this newsgroup want me to post information bulletins about the latest of Crohn’s Disease and MAP research? If people don’t want to hear about it, then I won’t post it any more. Sincerely, Alan Kennedy.

Response:

Alan, very well put.  And I for one would like you to continue the update and information on MAP.  Sorry about your mothers friend dying (the dog)  It is very hard emotionally.   Maybe in a  little time she can get another companion. UM MOM Susan

– Hide quoted text — Show quoted text – Hi All, I’ve been away for a few days, staying out in my mothers. Her 15 1/2 year old dog passed away on Monday. She was quite upset about it, because she’s had the dog since her husband (my father) passed away 15 years ago. So I went out to keep her company. On Monday, as I spent an hour burying the beloved pooch in the back garden, I had much time to reflect on life and death, happiness and unhappiness, healthiness and suffering. It was a sad time. The conclusion that I came to was the one that I always come to: That we are all lucky to have our time in this world. Some of us are less lucky, in that health problems sometimes prevent us from realising the fullness of our potential. It is particularly sad when this affects children. I realised then that I have an important job to do, and that it is not yet finished. I also realised if I’m going to achieve anything, then I need my full emotional strength, so as to be able to handle the inevitable accusations of self-interest that always arise. When I started out my long journey five years ago, I knew that I would come under sustained personal criticism, suspicion and attack. There are just too many vested interests involved for that not to be the case. It is ironic that by far the most vitriolic and anti-personal attacks originate from within the very group that I started out to help. Ironic, but not surprising, however, since the destructive nature of Crohn’s Disease forces us all to construct world pictures, sometimes based on assumptions and hopes, that permits us to live life without going insane. If someone challenges those assumptions and hopes, then it is only to be expected that we will sometimes strike out against that someone with vigorous force. I am fully aware that this is a support newsgroup. People come to this newsgroup for "Discussions of all types of medicine — conventional and alternative, Western and Eastern, your Aunt Harriet’s home remedies, whatever — are welcome here;", according to the Newsgroup charter. http://ascc.healingwell.com/info/charter.html I make posts into the newsgroup about MAP and Crohn’s Disease related news because I believe that people want to hear about them. Sometimes these announcements result in extensive debates, in which I endeavour to always support my point of view with research and facts. Many times, these debates get personal, and though I dislike being personally attacked for my point of view, I endeavour to not let it get under my skin, and to reply in a sensible and mature fashion. But some of these discussions of the previous two weeks have resulted in heated emotional discussions, with plenty of negative emotional energy flying around. Although I don’t feel responsible for infusing this negative emotional energy into the group, I still don’t want it to happen. I don’t want this newsgroup to be polluted with negative emotion, not only because it’s against the newsgroup charter, but it’s a waste of my and others valuable emotional energy. So, the question I put to the newsgroup is this: Do people in this newsgroup want me to post information bulletins about the latest of Crohn’s Disease and MAP research? If people don’t want to hear about it, then I won’t post it any more. Sincerely, Alan Kennedy.

Response:

Hi All, I’ve been away for a few days, staying out in my mothers. Her 15 1/2 year old dog passed away on Monday. She was quite upset about it, because she’s had the dog since her husband (my father) passed away 15 years ago. So I went out to keep her company. On Monday, as I spent an hour burying the beloved pooch in the back garden, I had much time to reflect on life and death, happiness and unhappiness, healthiness and suffering. It was a sad time. The conclusion that I came to was the one that I always come to: That we are all lucky to have our time in this world. Some of us are less lucky, in that health problems sometimes prevent us from realising the fullness of our potential. It is particularly sad when this affects children. I realised then that I have an important job to do, and that it is not yet finished. I also realised if I’m going to achieve anything, then I need my full emotional strength, so as to be able to handle the inevitable accusations of self-interest that always arise. When I started out my long journey five years ago, I knew that I would come under sustained personal criticism, suspicion and attack. There are just too many vested interests involved for that not to be the case. It is ironic that by far the most vitriolic and anti-personal attacks originate from within the very group that I started out to help. Ironic, but not surprising, however, since the destructive nature of Crohn’s Disease forces us all to construct world pictures, sometimes based on assumptions and hopes, that permits us to live life without going insane. If someone challenges those assumptions and hopes, then it is only to be expected that we will sometimes strike out against that someone with vigorous force. I am fully aware that this is a support newsgroup. People come to this newsgroup for "Discussions of all types of medicine — conventional and alternative, Western and Eastern, your Aunt Harriet’s home remedies, whatever — are welcome here;", according to the Newsgroup charter. http://ascc.healingwell.com/info/charter.html I make posts into the newsgroup about MAP and Crohn’s Disease related news because I believe that people want to hear about them. Sometimes these announcements result in extensive debates, in which I endeavour to always support my point of view with research and facts. Many times, these debates get personal, and though I dislike being personally attacked for my point of view, I endeavour to not let it get under my skin, and to reply in a sensible and mature fashion. But some of these discussions of the previous two weeks have resulted in heated emotional discussions, with plenty of negative emotional energy flying around. Although I don’t feel responsible for infusing this negative emotional energy into the group, I still don’t want it to happen. I don’t want this newsgroup to be polluted with negative emotion, not only because it’s against the newsgroup charter, but it’s a waste of my and others valuable emotional energy. So, the question I put to the newsgroup is this: Do people in this newsgroup want me to post information bulletins about the latest of Crohn’s Disease and MAP research? If people don’t want to hear about it, then I won’t post it any more. Sincerely, Alan Kennedy.

Response:

Newbie in despair–desperately needs encouragement and a hug

Question:

Steven- I think alot of companies are trying to be more flexible with telecommuting, etc.  I can  understand how you feel… I was out of work for 8 months when I was in a terrible flare.  Talking to a career counseler may be helpful.  Good luck, and don’t get discouraged. Be well- Tracy CD class of ‘98 my homepage: http://home.talkcity.com/ParadiseDr/goodboie/index.html  : )  smile – it makes people wonder what you’re up to!

Response:

Steven- I’m not sure where you are from, but I’m sure there are companies out there in search of a wonderful engineer.  

Due to my steadily declining state of health, I can no longer work full-time, I can no longer do any significant business traveling, and the last couple of winters I have been so sick that I couldn’t work at all. No employer wants that. I may need to think about finding some other line of work entirely. Maybe I need to talk to a career counselor. I could do tech writing from home, or something?? — Steven D. Litvintchouk                  

Response:

- Hide quoted text — Show quoted text – Hi, UM MOM Susan (sdores) recommended this NG to me, so I thought I would introduce myself. I’ve had irritable bowel syndrome (IBS) since I was 12–Librium, Donnatal, etc. etc. Actually, I managed to get it under good control. But now I have developed GERD, adult-onset asthma, chronic sinusitis, etc. etc. etc. This has necessitated changes to my diet and eating pattern, and I take lots more meds for all these conditions. All that has re-awakened my IBS (among many other side effects).  I had terrible cramping and mucosy diarrhea this morning. But the absolutely worst side effect I have ever experienced from any med, I have now experienced–inability to urinate.  That one sent me to the Emergency Room last week.  I panicked when that happened too–I got nauseous and got diarrhea and threw up right in the ER. (Think about how you would feel if you couldn’t urinate, and your bladder felt like it was about to burst.) And nobody cares.  Nobody.  Nowhere. I’m just at the end of my rope. I can’t deal with all these different conditions simultaneously, with all the meds and the side effects and the drug interactions among them all. I’ve fought and fought and fought, but my optimism has now ebbed. My illness reached a point where I was unable to work as an engineer as I used to. First major budget cut came (after 9-11), and I was laid off. I’ve hit bottom. I DESPERATELY need a hug, some encouragement, something. From anybody.  From anywhere. Thanx in advance! hey steve

(((((((((((((steve)))))))))))))))) its annie and i bet you "know" me.. you are the first person i am writing to on here…my puter has been up and down..we have been away…i cannot guarantee much til lthis is fixed..but for now 1)when u hit bottom..the only place is up…i KNOW thats a dumb cliche..but its true 2)the illnesses and symptoms will not be with you all the time…chronic things are .well.."chronic" meaning u will "have them" but the symptoms may abate and it will be like a time out from any pain etc..you gotta hang in til then 3)together in this group alone we practically fund the er’s across the country..you will spend time in them..and in doctor’s offices..and in walk in clinics at times..and in the hospital itself(which is heaven if you like lime jello, luke warm yuck-brand tea and cereal which looks like…and tastes like..well never mind…) but it happens and it happens to all of us..we end up in the er for this..that or the other…sometimes we get admitted(i almost said "committed" cos it feels like that too) sometimes not…and not knowing quite what is causing whatever is happening is the scary part…but you find out soon enough(sometimes ignorance is bliss..but it does make one frightened..me..i would rather know the worst than worry about what probably isnt..) 4) you are NOT alone…not in the world…there are lots of people ill out there..on this board and not on this board…with or without employment(thats why God created disability <g) steve..i have lost not only a job but my entire career…my first husband(if u can call that a loss) and friends who didnt believe i was sick…i have been where you are…and sometimes make a leap back there in bad moments.. you will be all right..not healthy totally…you may have a different job for a while..the economy is supposed to get better..eventually…and you will be able to find work…in your area(what kind of engineer? my husband..number two ..is a software engineer)..gee..an engineer who WRITES? you are unusual already !!!(my son is an engineer too..sort of plant, facilities and environmental…no dont ask…i cannot explain)..he doesnt write on newsgroups either…what you have to find steve..is something to hang on to…like…God…or if you dont believe..your mother who is great…she loves you ..gee..i know that for sure…or if you dont feel like hangin’ on to mom for now…humor…anything..actually..you just reach out and hang on to me..i make a good hanger on person..OUCH…not my neck…hang on but watch the neck..please<g and steve you are HERE.wow…you couldnt be in a better place on the net…i havent read the responses yet..but i bet you get a ton of support, encouragement and info on here…i know i do ..(here it is almost 2am and i am here cos i cnanot sleep..its that or wake up the cats for company).. so again(((((((((((((((((((((steve)))))))))))))))))))))))))))) and know you are loved..big time annie in boston(well you said "anywhere" and its as good a place as any

Response:

Steven- I’m not sure where you are from, but I’m sure there are companies out there in search of a wonderful engineer.  I can understand the toll that the stress of interviewing would bring, though.  I have been extremely lucky with my job.  I even have permission to work from home on occasion if I feel I can’t make it to work. You are more than welcome here.  Hope to "see you around" the newsgroup. Be well- Tracy CD class of ‘98 my homepage: http://home.talkcity.com/ParadiseDr/goodboie/index.html  : )  smile – it makes people wonder what you’re up to!

Response:

Boy did I laugh!!!  thanks.  But today started out so wonderfully that sick or not sick, I am such a happy camper!  UM MOM Susan

– Hide quoted text — Show quoted text – Those would be the "black sheep" of our family. . . <grin Rebecca :-) Don’t worry, I don’t think he is that sensitive.  Plus I didn’t take it as wanting him to leave at all, I just wanted to let you know that maybe a lot of the IBS folks are at that group.  I appreciate how everyone is welcoming Steve, though I knew you all would.  He is a good person and I think all will take him into the family,  ok a few might not and not mentioning any names ;) ))  UM MOM Susan Hi Susan: I totally agree — I hope my post didn’t sound like I wanted him to leave — just the opposite. I was just wondering outloud why we don’t have more IBS posters —- Sorry for the confusion. Rebecca :-) Rebecca, there is a IBS newsgroup, but I wanted Steven to come here for a specific reason, we are like family and support, joke and everything in between.  Steven needs a good support group to talk about any of the medical problems he has.  He is a good man and will give lots to this group. UM MOM Susan Welcome Steve! We’re glad you found us! Just a "head’s up" NA — I’m pretty sure the original charter for this ng includes IBS — perhaps Sue will reprint it so we can be sure. (Thanks Sue). For some reason we just don’t have a lot of IBS people posting — I wonder if there is a ng specifically for them that wasn’t around when this ng was formed? In any event, many here were first dxed with IBS only to find out later that is was, instead, IBD. Many of the symptoms/problems are the same and we can learn from each other’s experiences. I know a number of people here have also had trouble with GERD, so perhaps someone else can help Steve with that problem. Anyhow, just wanted to welcome Steve and send along a few hugs ((( ))). I hope by the time you read this, you are feeling a little better. Rebecca :-) Hi, UM MOM Susan (sdores) recommended this NG to me, so I thought I would introduce myself. I’ve had irritable bowel syndrome (IBS) since I was 12–Librium, Donnatal, etc. etc. Actually, I managed to get it under good control. But now I have developed GERD, You need to check out this web site: http://www.iffgd.org That organization, IFFGD, specializes in functional gastrointestinal disorders, which include IBS and GERD. This newsgroup, on the other hand, is about IBD, which is an organic illness–something different from what you have. Best of luck to you. Both IBS and GERD are very treatable.

Response:

Those would be the "black sheep" of our family. . . <grin Rebecca :-)

– Hide quoted text — Show quoted text – Don’t worry, I don’t think he is that sensitive.  Plus I didn’t take it as wanting him to leave at all, I just wanted to let you know that maybe a lot of the IBS folks are at that group.  I appreciate how everyone is welcoming Steve, though I knew you all would.  He is a good person and I think all will take him into the family,  ok a few might not and not mentioning any names ;) ))  UM MOM Susan Hi Susan: I totally agree — I hope my post didn’t sound like I wanted him to leave — just the opposite. I was just wondering outloud why we don’t have more IBS posters —- Sorry for the confusion. Rebecca :-) Rebecca, there is a IBS newsgroup, but I wanted Steven to come here for a specific reason, we are like family and support, joke and everything in between.  Steven needs a good support group to talk about any of the medical problems he has.  He is a good man and will give lots to this group. UM MOM Susan Welcome Steve! We’re glad you found us! Just a "head’s up" NA — I’m pretty sure the original charter for this ng includes IBS — perhaps Sue will reprint it so we can be sure. (Thanks Sue). For some reason we just don’t have a lot of IBS people posting — I wonder if there is a ng specifically for them that wasn’t around when this ng was formed? In any event, many here were first dxed with IBS only to find out later that is was, instead, IBD. Many of the symptoms/problems are the same and we can learn from each other’s experiences. I know a number of people here have also had trouble with GERD, so perhaps someone else can help Steve with that problem. Anyhow, just wanted to welcome Steve and send along a few hugs ((( ))). I hope by the time you read this, you are feeling a little better. Rebecca :-) Hi, UM MOM Susan (sdores) recommended this NG to me, so I thought I would introduce myself. I’ve had irritable bowel syndrome (IBS) since I was 12–Librium, Donnatal, etc. etc. Actually, I managed to get it under good control. But now I have developed GERD, You need to check out this web site: http://www.iffgd.org That organization, IFFGD, specializes in functional gastrointestinal disorders, which include IBS and GERD. This newsgroup, on the other hand, is about IBD, which is an organic illness–something different from what you have. Best of luck to you. Both IBS and GERD are very treatable.

Response:

Don’t worry, I don’t think he is that sensitive.  Plus I didn’t take it as wanting him to leave at all, I just wanted to let you know that maybe a lot of the IBS folks are at that group.  I appreciate how everyone is welcoming Steve, though I knew you all would.  He is a good person and I think all will take him into the family,  ok a few might not and not mentioning any names ;) ))  UM MOM Susan

– Hide quoted text — Show quoted text – Hi Susan: I totally agree — I hope my post didn’t sound like I wanted him to leave — just the opposite. I was just wondering outloud why we don’t have more IBS posters —- Sorry for the confusion. Rebecca :-) Rebecca, there is a IBS newsgroup, but I wanted Steven to come here for a specific reason, we are like family and support, joke and everything in between.  Steven needs a good support group to talk about any of the medical problems he has.  He is a good man and will give lots to this group.  UM MOM Susan Welcome Steve! We’re glad you found us! Just a "head’s up" NA — I’m pretty sure the original charter for this ng includes IBS — perhaps Sue will reprint it so we can be sure. (Thanks Sue). For some reason we just don’t have a lot of IBS people posting — I wonder if there is a ng specifically for them that wasn’t around when this ng was formed? In any event, many here were first dxed with IBS only to find out later that is was, instead, IBD. Many of the symptoms/problems are the same and we can learn from each other’s experiences. I know a number of people here have also had trouble with GERD, so perhaps someone else can help Steve with that problem. Anyhow, just wanted to welcome Steve and send along a few hugs ((( ))). I hope by the time you read this, you are feeling a little better. Rebecca :-) Hi, UM MOM Susan (sdores) recommended this NG to me, so I thought I would introduce myself. I’ve had irritable bowel syndrome (IBS) since I was 12–Librium, Donnatal, etc. etc. Actually, I managed to get it under good control. But now I have developed GERD, You need to check out this web site: http://www.iffgd.org That organization, IFFGD, specializes in functional gastrointestinal disorders, which include IBS and GERD. This newsgroup, on the other hand, is about IBD, which is an organic illness–something different from what you have. Best of luck to you. Both IBS and GERD are very treatable.

Response:

Welcome, Steven!  Hugs and encouraging thoughts being sent your way.  Hope you are feeling better soon! Get/stay healthy, Kathi

Response:

Hi Susan: I totally agree — I hope my post didn’t sound like I wanted him to leave — just the opposite. I was just wondering outloud why we don’t have more IBS posters —- Sorry for the confusion. Rebecca :-)

– Hide quoted text — Show quoted text – Rebecca, there is a IBS newsgroup, but I wanted Steven to come here for a specific reason, we are like family and support, joke and everything in between.  Steven needs a good support group to talk about any of the medical problems he has.  He is a good man and will give lots to this group.  UM MOM Susan Welcome Steve! We’re glad you found us! Just a "head’s up" NA — I’m pretty sure the original charter for this ng includes IBS — perhaps Sue will reprint it so we can be sure. (Thanks Sue). For some reason we just don’t have a lot of IBS people posting — I wonder if there is a ng specifically for them that wasn’t around when this ng was formed? In any event, many here were first dxed with IBS only to find out later that is was, instead, IBD. Many of the symptoms/problems are the same and we can learn from each other’s experiences. I know a number of people here have also had trouble with GERD, so perhaps someone else can help Steve with that problem. Anyhow, just wanted to welcome Steve and send along a few hugs ((( ))). I hope by the time you read this, you are feeling a little better. Rebecca :-) Hi, UM MOM Susan (sdores) recommended this NG to me, so I thought I would introduce myself. I’ve had irritable bowel syndrome (IBS) since I was 12–Librium, Donnatal, etc. etc. Actually, I managed to get it under good control. But now I have developed GERD, You need to check out this web site: http://www.iffgd.org That organization, IFFGD, specializes in functional gastrointestinal disorders, which include IBS and GERD. This newsgroup, on the other hand, is about IBD, which is an organic illness–something different from what you have. Best of luck to you. Both IBS and GERD are very treatable.

Response:

Rebecca, there is a IBS newsgroup, but I wanted Steven to come here for a specific reason, we are like family and support, joke and everything in between.  Steven needs a good support group to talk about any of the medical problems he has.  He is a good man and will give lots to this group.  UM MOM Susan

– Hide quoted text — Show quoted text – Welcome Steve! We’re glad you found us! Just a "head’s up" NA — I’m pretty sure the original charter for this ng includes IBS — perhaps Sue will reprint it so we can be sure. (Thanks Sue). For some reason we just don’t have a lot of IBS people posting — I wonder if there is a ng specifically for them that wasn’t around when this ng was formed? In any event, many here were first dxed with IBS only to find out later that is was, instead, IBD. Many of the symptoms/problems are the same and we can learn from each other’s experiences. I know a number of people here have also had trouble with GERD, so perhaps someone else can help Steve with that problem. Anyhow, just wanted to welcome Steve and send along a few hugs ((( ))). I hope by the time you read this, you are feeling a little better. Rebecca :-) Hi, UM MOM Susan (sdores) recommended this NG to me, so I thought I would introduce myself. I’ve had irritable bowel syndrome (IBS) since I was 12–Librium, Donnatal, etc. etc. Actually, I managed to get it under good control. But now I have developed GERD, You need to check out this web site: http://www.iffgd.org That organization, IFFGD, specializes in functional gastrointestinal disorders, which include IBS and GERD. This newsgroup, on the other hand, is about IBD, which is an organic illness–something different from what you have. Best of luck to you. Both IBS and GERD are very treatable.

Response:

Hi Sue, Thanks for letting Steven know that he is also welcome here.  But did you have to do the charter again?!  ;o)))   How you doing?  UM MOM Susan

– Hide quoted text — Show quoted text – Hi, UM MOM Susan (sdores) recommended this NG to me, so I thought I would introduce myself. I’ve had irritable bowel syndrome (IBS) since I was 12–Librium, Donnatal, etc. etc. Actually, I managed to get it under good control. But now I have developed GERD, You need to check out this web site: http://www.iffgd.org That organization, IFFGD, specializes in functional gastrointestinal disorders, which include IBS and GERD. This newsgroup, on the other hand, is about IBD, which is an organic illness–something different from what you have. Best of luck to you. Both IBS and GERD are very treatable. One correction to the above: IBS’ers are welcome here and indeed were included from the beginning, as evidenced by the ng charter: What is Alt.support.crohns-colitis? Alt.support.crohns-colitis was created in early 1994 as a forum where people suffering from ulcerative colitis, Crohn’s Disease, and irritable bowel syndrome can share their everyday struggles with these illnesses, as well as discuss medicines, treatments, surgery, diet, health care providers, related illnesses, and anything else anyone can think of that relates to these diseases.  In other words, this is the online equivalent of a support group, which means that no question is stupid and no condition embarrassing here.  It also means we’re all here to help each other out, so please be nice, be polite, and no flaming. Discussions of all types of medicine- conventional and alternative, Western and Eastern, your Aunt Harriet’s home remedies, whatever- are welcome here; however, any person discussing a potential remedy which he or she also sells must explicitly begin the "Subject" header of their post with the word "AD" or "ADVERTISEMENT" in all caps, regardless of whether or not they profit from such sales.  Spamming is expressly forbidden as violating the rules of netiquette as well as those of this newsgroup.  Finally, please keep in mind that no one knows what causes these illnesses, no one’s come up with a cure, and we need all the help we can get.

Response:

NA, he is still welcome to be here and I hope you agree with this.  But all have always been welcomed and Steven can get a lot of help from our group. UM MOM Susan

– Hide quoted text — Show quoted text – Hi, UM MOM Susan (sdores) recommended this NG to me, so I thought I would introduce myself. I’ve had irritable bowel syndrome (IBS) since I was 12–Librium, Donnatal, etc. etc. Actually, I managed to get it under good control. But now I have developed GERD, You need to check out this web site: http://www.iffgd.org That organization, IFFGD, specializes in functional gastrointestinal disorders, which include IBS and GERD. This newsgroup, on the other hand, is about IBD, which is an organic illness–something different from what you have. Best of luck to you. Both IBS and GERD are very treatable.

Response:

    Jesus, Steven…..I was laid off last July and am pretty much the same boat. I haven’t worked since then and have to be slective about what I look at for work because I have been so ill this last yeat. It seems when one issue clears up another begins adn occasionally I even get a break of a week or two with nothing major going haywire.     So, I can feel for you. If you figure something out, let me know. Thus far I have been helped by fmaily and friends, but how much of a burden can one expect them to take up? If I add my still running divorce on top of all that, I might actually get to see solvency in the next couple of lifetimes ( having to file bankruptcy because my ex never paid a single medical bill ). – Hide quoted text — Show quoted text – Hi Steven, Welcome, thank you Susan for introducing you to us. I’m not sure if I can help with your conditions other then tell you that your not alone in how your feelling. many of us have had these types of problems, ER that don’t respond correctly, doctors that give bad advise, and the disease takes over our lives at times. All I can say is to keep fighting, look for new doctors that do care- they are out there. and some how things do get better. The work thing is hard enough on it’s own, do you still have insurance I hope, don’t let that lapse if anyway possible. I was laid off from work a few months ago. My COBRA health insurance expires next year. I’m currently living off my savings. And I can’t even think about looking for another job in my precarious state of health. Even assuming that there are companies who will hire an engineer like me on a part-time basis with no travel (that’s the only way I was able to work at all in the year until I got laid off).

– Cry havoc! and let loose the dogs of war….. — William Shakespeare

Response:

Hi Steven can’t begin to understand how you fee as my own problems are different. But what I do know is that this Group is fantastic. A while ago, and more than likely in the future too, I needed help and support. Had loads of replies of support from people who genuinely care, and best of all those lovely {{{hugs}}} from around the world. Come back time and time again. Have a whinge and moan, and shout like hell when it hurts, we are all here listening for you. Sorry, can’t find all the words to support you but that’s the best I can do. God bless  {{{hugs}}} Pete — Outgoing mail is certified Virus Free. Checked by Expert Anti-Virus.

Response:

Rebecca, you are right.  Back in Feb, when the "specialist" said I had IBS and not CD, I was concerned. Sue posted the charter, and IBS is part of the group. Steve, welcome. You have found a wonderful place.  I’ve been gone for a while.  I completely understand your frustration and despair.  I’ve been floating around that space myself.  I too have adult onset asthma.  I know what difficulties it causes.  All I can say is that you came to a good place to get your spirits lifted, to find encouragement and advice.  And hugs. something, ANYTHING, for YOU that helps you relax.  For me, it’s movies and crochet.  Whatever it is, find something just for you. — : ) Mrs. 9 Cats Everything I know I learned from Mr. Spock

– Hide quoted text — Show quoted text – Welcome Steve! We’re glad you found us! Just a "head’s up" NA — I’m pretty sure the original charter for this ng includes IBS — perhaps Sue will reprint it so we can be sure. (Thanks Sue). For some reason we just don’t have a lot of IBS people posting — I wonder if there is a ng specifically for them that wasn’t around when this ng was formed? In any event, many here were first dxed with IBS only to find out later that is was, instead, IBD. Many of the symptoms/problems are the same and we can learn from each other’s experiences. I know a number of people here have also had trouble with GERD, so perhaps someone else can help Steve with that problem. Anyhow, just wanted to welcome Steve and send along a few hugs ((( ))). I hope by the time you read this, you are feeling a little better. Rebecca :-) Hi, UM MOM Susan (sdores) recommended this NG to me, so I thought I would introduce myself. I’ve had irritable bowel syndrome (IBS) since I was 12–Librium, Donnatal, etc. etc. Actually, I managed to get it under good control. But now I have developed GERD, You need to check out this web site: http://www.iffgd.org That organization, IFFGD, specializes in functional gastrointestinal disorders, which include IBS and GERD. This newsgroup, on the other hand, is about IBD, which is an organic illness–something different from what you have. Best of luck to you. Both IBS and GERD are very treatable.

Response:

Yeah! You beat me to it! Great minds think alike <VVEG Rebecca :-) who thanks Sue and hopes she is feeling well.

– Hide quoted text — Show quoted text – Hi, UM MOM Susan (sdores) recommended this NG to me, so I thought I would introduce myself. I’ve had irritable bowel syndrome (IBS) since I was 12–Librium, Donnatal, etc. etc. Actually, I managed to get it under good control. But now I have developed GERD, You need to check out this web site: http://www.iffgd.org That organization, IFFGD, specializes in functional gastrointestinal disorders, which include IBS and GERD. This newsgroup, on the other hand, is about IBD, which is an organic illness–something different from what you have. Best of luck to you. Both IBS and GERD are very treatable. One correction to the above: IBS’ers are welcome here and indeed were included from the beginning, as evidenced by the ng charter: What is Alt.support.crohns-colitis? Alt.support.crohns-colitis was created in early 1994 as a forum where people suffering from ulcerative colitis, Crohn’s Disease, and irritable bowel syndrome can share their everyday struggles with these illnesses, as well as discuss medicines, treatments, surgery, diet, health care providers, related illnesses, and anything else anyone can think of that relates to these diseases.  In other words, this is the online equivalent of a support group, which means that no question is stupid and no condition embarrassing here.  It also means we’re all here to help each other out, so please be nice, be polite, and no flaming. Discussions of all types of medicine- conventional and alternative, Western and Eastern, your Aunt Harriet’s home remedies, whatever- are welcome here; however, any person discussing a potential remedy which he or she also sells must explicitly begin the "Subject" header of their post with the word "AD" or "ADVERTISEMENT" in all caps, regardless of whether or not they profit from such sales.  Spamming is expressly forbidden as violating the rules of netiquette as well as those of this newsgroup.  Finally, please keep in mind that no one knows what causes these illnesses, no one’s come up with a cure, and we need all the help we can get.

Response:

Welcome Steve! We’re glad you found us! Just a "head’s up" NA — I’m pretty sure the original charter for this ng includes IBS — perhaps Sue will reprint it so we can be sure. (Thanks Sue). For some reason we just don’t have a lot of IBS people posting — I wonder if there is a ng specifically for them that wasn’t around when this ng was formed? In any event, many here were first dxed with IBS only to find out later that is was, instead, IBD. Many of the symptoms/problems are the same and we can learn from each other’s experiences. I know a number of people here have also had trouble with GERD, so perhaps someone else can help Steve with that problem. Anyhow, just wanted to welcome Steve and send along a few hugs ((( ))). I hope by the time you read this, you are feeling a little better. Rebecca :-)

– Hide quoted text — Show quoted text – Hi, UM MOM Susan (sdores) recommended this NG to me, so I thought I would introduce myself. I’ve had irritable bowel syndrome (IBS) since I was 12–Librium, Donnatal, etc. etc. Actually, I managed to get it under good control. But now I have developed GERD, You need to check out this web site: http://www.iffgd.org That organization, IFFGD, specializes in functional gastrointestinal disorders, which include IBS and GERD. This newsgroup, on the other hand, is about IBD, which is an organic illness–something different from what you have. Best of luck to you. Both IBS and GERD are very treatable.

Response:

– Hide quoted text — Show quoted text – Hi, UM MOM Susan (sdores) recommended this NG to me, so I thought I would introduce myself. I’ve had irritable bowel syndrome (IBS) since I was 12–Librium, Donnatal, etc. etc. Actually, I managed to get it under good control. But now I have developed GERD, You need to check out this web site: http://www.iffgd.org That organization, IFFGD, specializes in functional gastrointestinal disorders, which include IBS and GERD. This newsgroup, on the other hand, is about IBD, which is an organic illness–something different from what you have. Best of luck to you. Both IBS and GERD are very treatable.

One correction to the above: IBS’ers are welcome here and indeed were included from the beginning, as evidenced by the ng charter: What is Alt.support.crohns-colitis? Alt.support.crohns-colitis was created in early 1994 as a forum where people suffering from ulcerative colitis, Crohn’s Disease, and irritable bowel syndrome can share their everyday struggles with these illnesses, as well as discuss medicines, treatments, surgery, diet, health care providers, related illnesses, and anything else anyone can think of that relates to these diseases.  In other words, this is the online equivalent of a support group, which means that no question is stupid and no condition embarrassing here.  It also means we’re all here to help each other out, so please be nice, be polite, and no flaming. Discussions of all types of medicine- conventional and alternative, Western and Eastern, your Aunt Harriet’s home remedies, whatever- are welcome here; however, any person discussing a potential remedy which he or she also sells must explicitly begin the "Subject" header of their post with the word "AD" or "ADVERTISEMENT" in all caps, regardless of whether or not they profit from such sales.  Spamming is expressly forbidden as violating the rules of netiquette as well as those of this newsgroup.  Finally, please keep in mind that no one knows what causes these illnesses, no one’s come up with a cure, and we need all the help we can get.

Response:

Hi, UM MOM Susan (sdores) recommended this NG to me, so I thought I would introduce myself. I’ve had irritable bowel syndrome (IBS) since I was 12–Librium, Donnatal, etc. etc. Actually, I managed to get it under good control. But now I have developed GERD,

You need to check out this web site: http://www.iffgd.org That organization, IFFGD, specializes in functional gastrointestinal disorders, which include IBS and GERD. This newsgroup, on the other hand, is about IBD, which is an organic illness–something different from what you have. Best of luck to you. Both IBS and GERD are very treatable.

Response:

Hi Steven, Welcome, thank you Susan for introducing you to us. I’m not sure if I can help with your conditions other then tell you that your not alone in how your feelling. many of us have had these types of problems, ER that don’t respond correctly, doctors that give bad advise, and the disease takes over our lives at times. All I can say is to keep fighting, look for new doctors that do care- they are out there. and some how things do get better. The work thing is hard enough on it’s own, do you still have insurance I hope, don’t let that lapse if anyway possible.

I was laid off from work a few months ago. My COBRA health insurance expires next year. I’m currently living off my savings. And I can’t even think about looking for another job in my precarious state of health. Even assuming that there are companies who will hire an engineer like me on a part-time basis with no travel (that’s the only way I was able to work at all in the year until I got laid off). — Steven D. Litvintchouk                  

Response:

Hi Steven, Welcome, thank you Susan for introducing you to us. I’m not sure if I can help with your conditions other then tell you that your not alone in how your feelling. many of us have had these types of problems, ER that don’t respond correctly, doctors that give bad advise, and the disease takes over our lives at times. All I can say is to keep fighting, look for new doctors that do care- they are out there. and some how things do get better. The work thing is hard enough on it’s own, do you still have insurance I hope, don’t let that lapse if anyway possible. Do you have any support that can help you financially so you can focus on your health for now?  I’ve been there to and it’s very hard our work gives us so many things other then money.. I hope you can see through this and that you may need this time to get healthy. Let us know if we can help in anyway. Leeann

Response:

Hi Steven, glad Susan directed you our way. First here are lots of {{{{{hugs}}}} for you. I think we all have felt rock bottom as you do, but just try to keep in mind that there can be better times ahead. And though it may not always seem like like there are alot of people who care…this is a great bunch of people who can relate to what you are feeling, so lean on us whenever you want. Alot of times just writing it out even helps :-) Take care and try to get some rest Lisa :-) Happiness makes up in height for what it lacks in length ~Robert Frost

Response:

Hi Steven, I am new here as well but if there is anything I can do for you I am here to listen if nothing else.  This is really a great group. Jean

– Hide quoted text — Show quoted text – Hi, UM MOM Susan (sdores) recommended this NG to me, so I thought I would introduce myself. I’ve had irritable bowel syndrome (IBS) since I was 12–Librium, Donnatal, etc. etc. Actually, I managed to get it under good control. But now I have developed GERD, adult-onset asthma, chronic sinusitis, etc. etc. etc. This has necessitated changes to my diet and eating pattern, and I take lots more meds for all these conditions. All that has re-awakened my IBS (among many other side effects).  I had terrible cramping and mucosy diarrhea this morning. But the absolutely worst side effect I have ever experienced from any med, I have now experienced–inability to urinate.  That one sent me to the Emergency Room last week.  I panicked when that happened too–I got nauseous and got diarrhea and threw up right in the ER. (Think about how you would feel if you couldn’t urinate, and your bladder felt like it was about to burst.) And nobody cares.  Nobody.  Nowhere. I’m just at the end of my rope. I can’t deal with all these different conditions simultaneously, with all the meds and the side effects and the drug interactions among them all. I’ve fought and fought and fought, but my optimism has now ebbed. My illness reached a point where I was unable to work as an engineer as I used to. First major budget cut came (after 9-11), and I was laid off. I’ve hit bottom. I DESPERATELY need a hug, some encouragement, something. From anybody.  From anywhere. Thanx in advance! — Steven L.

Response:

Hi Steven and I am glad you came.Everyone Steven is having a real hard time and needs some major support esp emotionally.  I know you will all welcome him to our family.  Talk to you tomorrow Steven got to get to bed.  Flu. and flare.  UM MOM Susan

– Hide quoted text — Show quoted text – Hi, UM MOM Susan (sdores) recommended this NG to me, so I thought I would introduce myself. I’ve had irritable bowel syndrome (IBS) since I was 12–Librium, Donnatal, etc. etc. Actually, I managed to get it under good control. But now I have developed GERD, adult-onset asthma, chronic sinusitis, etc. etc. etc. This has necessitated changes to my diet and eating pattern, and I take lots more meds for all these conditions. All that has re-awakened my IBS (among many other side effects).  I had terrible cramping and mucosy diarrhea this morning. But the absolutely worst side effect I have ever experienced from any med, I have now experienced–inability to urinate.  That one sent me to the Emergency Room last week.  I panicked when that happened too–I got nauseous and got diarrhea and threw up right in the ER. (Think about how you would feel if you couldn’t urinate, and your bladder felt like it was about to burst.) And nobody cares.  Nobody.  Nowhere. I’m just at the end of my rope. I can’t deal with all these different conditions simultaneously, with all the meds and the side effects and the drug interactions among them all. I’ve fought and fought and fought, but my optimism has now ebbed. My illness reached a point where I was unable to work as an engineer as I used to. First major budget cut came (after 9-11), and I was laid off. I’ve hit bottom. I DESPERATELY need a hug, some encouragement, something. From anybody.  From anywhere. Thanx in advance! — Steven L.

Response:

Hi, UM MOM Susan (sdores) recommended this NG to me, so I thought I would introduce myself. I’ve had irritable bowel syndrome (IBS) since I was 12–Librium, Donnatal, etc. etc. Actually, I managed to get it under good control. But now I have developed GERD, adult-onset asthma, chronic sinusitis, etc. etc. etc. This has necessitated changes to my diet and eating pattern, and I take lots more meds for all these conditions. All that has re-awakened my IBS (among many other side effects).  I had terrible cramping and mucosy diarrhea this morning. But the absolutely worst side effect I have ever experienced from any med, I have now experienced–inability to urinate.  That one sent me to the Emergency Room last week.  I panicked when that happened too–I got nauseous and got diarrhea and threw up right in the ER. (Think about how you would feel if you couldn’t urinate, and your bladder felt like it was about to burst.) And nobody cares.  Nobody.  Nowhere. I’m just at the end of my rope. I can’t deal with all these different conditions simultaneously, with all the meds and the side effects and the drug interactions among them all. I’ve fought and fought and fought, but my optimism has now ebbed. My illness reached a point where I was unable to work as an engineer as I used to. First major budget cut came (after 9-11), and I was laid off. I’ve hit bottom. I DESPERATELY need a hug, some encouragement, something. From anybody.  From anywhere. Thanx in advance! — Steven L.

Response:

To ALL Persons Getting Their Supplies Thru Medicare

Question:

Boy, I blew that one.  And my foot is bigger than my mouth.  I am still straining. — PcolaPhil  When I read about the evils of drinking, I gave up reading.                                               – -Henny Youngman "NewzDesk" <InTheP…@none.com

wrote in message

news:3d1106c2$1_2@spamkiller.newsgroups.com… | | "PcolaPhil" <flaretph…@earthlink.net

wrote in message

| news:OANP8.3294$Fv1.382403@newsread2.prod.itd.earthlink.net… |

Ignore my previous John.  I shot from the hip without

thinking. |

My foot tastes horrible.

|

|

PcolaPhil

| | I’ll mail you my recipe for a wonderful foot-topping seasoning mix, Pcola. I | always keep a fresh container on hand just for this purpose. (Even carry a | supply in my purse.) |  ;-) | Newz | | |

Response:

On Fri, 21 Jun 2002 23:30:07 GMT, "PcolaPhil" <flaretph…@earthlink.net

wrote: Bill, Medicare is a government health program setup to care for citizens exceeding the age of 65. Hope that this helps you understand Medicare a bit better, if not just ask away Bill.

It makes quite a few things clearer.  Thanks for the post.  Health care provision in Europe is very different from that in the US, and I have to remember this before putting fingers to keyboard. — Bill http://billnot.com

Response:

Subject: Re: To ALL Persons Getting Their Supplies-PART II From: "harmonica" harmonica…@hotmail.zzn.com I understand your concern for quality control. And there’s no question that our products are manufactured in the US. I’ve really never had any problem with the quality of Convatec

UK, Australia and New Zealand procure  ostomy equipment that comply with specified performance standards. Ostomy equipment distributed in the European Union must be certified to comply with ISO/CEN standards. In the US, manufacturers of ostomy products are not required to comply with any performance standards. Since  quality control has a statistical base (there must be an occasional failed lot or batch) it causes me to wonder: What do the US manufacturers do with the ostomy equipment that fail the ISO/CEN standards.

Response:

Bill, Medicare is a government health program setup to care for citizens exceeding the age of 65.  There are exceptions to this though, it also cares for indigent personnel in some cases and/or other classes of citizens who have problems for which Medicare is setup to support.  coverage and payment is setup in two classes: Part A – pertains to hospital care, what is covered with hospital care and how long, and charges that Medicare will allow and pay for under this provision.  Part B – pertains to physician care, conditions covered, how much each conditions receives in reimbursement.  Part B is only in effect if the patient elects it and pays a $50 monthly fee.  Medicare then pays 80% of charges IT says is authorized.  The other 20% is paid by the patient, or an insurance company if the patient has one.  Almost all ostomy supplies are covered by Medicare for payment, and the quantities allowed are good for most people. Coverage of supplies is real good as of now, but reimbursement to producers is dismal and getting worse if this setback is allowed. Many ostomy supplies producers or carriers will not accept Medicare assignment due to the low reimbursement rates allowed. Not the best solution I grant you, but I would fight like hell if this country tries to go to Socialized medicine.  I lived that type of care for 20 years in the Army (a very good taste of socialized medicine), and it is worse! Hope that this helps you understand Medicare a bit better, if not just ask away Bill. — PcolaPhil  When I read about the evils of drinking, I gave up reading.                                               – -Henny Youngman "Bill Hayles" <bill…@billnot.com

wrote in message

news:aepki2.44.1@billnot.com… | On Tue, 18 Jun 2002 09:41:10 -0700, "NewzDesk" <InTheP…@none.com

| wrote:

| |

|

Thanks for your support, John.  This actually affects

ostomates worldwide. |

As far as I know, except for Dansac and Eakin, all other major

ostomy supply |

manufacturers are in the US.

| | Braun?  Welland?  Clinimed? | |

Most of the ostomy supplies used

|

internationally are the same ones we use here.  What you wear

in Australia |

comes from the US – where there are no quality controls

appropriate to our |

appliances/supplies/accessories – due to the FDA

classification. | | What I wear in Spain, although nominally the same (Braun Biotrol) is | subtly different from the product I received in the UK.  The | *perfect* bag would be somewhere between the two. | | |

|

Speaking of suppliers/distributors: FWIW, Convatec is the

distributor for |

Eakin seals in the US and various other countries. Australia

uses Omnigon as |

it’s distributor for Eakin. As long as Eakin products continue

to be |

produced in Ireland by the same company we’re safe.

| | Agreed.  Eakin specially ship their seals to me, as they have no | Spanish agent.  Could you see a major player doing that? | | As an aside, for we non-US citizens, could somebody explain how | Medicare works?  I understand the general idea, but not why some | people get it and others don’t, and why it’s considered a last | resort. | | | — | | Bill | http://billnot.com |

Response:

Thanks for the back-up N.D.  The emphasis is much needed and it is time for folks to awaken from their dream state and get fighting mad. — PcolaPhil  When I read about the evils of drinking, I gave up reading.                                               – -Henny Youngman "NewzDesk" <InTheP…@none.com

wrote in message

news:3d0ecad7_1@spamkiller.newsgroups.com… | Part II | | 4. con’t | | Manufacturers do not want ostomy supplies’ coverage dropped because like any | medication that goes from a prescription form to over-the-counter, the price | can drop as much as 80%.  I don’t think I will see a box of wafer for $3 in | my lifetime.  Those of you who use catheters, what about $1/doz? Who’s more | powerful? The insurance industry or manufacturers of ostomy supplies? | | The pharmaceutical corps that most of the supply manufacturers are related | to are NOT going to spend a dime or time against their blood-brothers, the | Insurance Industry, in order to save the ostomy supply business as it exists | today. For one thing, ‘IT’S NOT COST EFFECTIVE". Insurance and pharm | industries will continue profits in the billions without the supply | manufacturers.  The "supply industry" may well be restructured one day – by | their own "family". | | I probably need to tone this down a little but am in a hurry. These are my | opinions. I believe in capitalism too, I am not opposed to anyone and | everyone making enormous profits and becoming billionaires. What I don’t | like is the continued unconscionable price-gouging of these industries. | Their utter disregard for consumers and patients. | | It’s situations just like this "revision" of the reimbursement charges for | Medicare that are quietly happening, one by one, ten by ten, state by state, | agency by agency, getting by most of the population unnoticed. And for the | most part, unchallenged. UOA fought and worked tirelessly to obtain the | increase in the monthly amounts allowed in the first place. It went into | effect  April 1 2001. This is June 2002. | | Ostomates are at the bottom of the barrel. Still the invisible population. | | As PcolaPhil said, "This is one of those occasions when we might indeed be | the masters of our fate.  What we do or don’t do can make the difference. | My e-mail is in…" Mine will be too. | | NewzDesk | addyahoodotcom4reply | | |

Response:

"PcolaPhil" <flaretph…@earthlink.net

wrote in message

news:OANP8.3294$Fv1.382403@newsread2.prod.itd.earthlink.net…

Ignore my previous John.  I shot from the hip without thinking. My foot tastes horrible. PcolaPhil

I’ll mail you my recipe for a wonderful foot-topping seasoning mix, Pcola. I always keep a fresh container on hand just for this purpose. (Even carry a supply in my purse.)  ;-) Newz

Response:

I understand your concern for quality control. And there’s no question that our products are manufactured in the US. I’ve really never had any problem with the quality of Convatec or any other products I’ve used. Dansac is the main 2 piece that I use. But I’ll supplement that with either Convatec/Coloplast to give my skin a break. I’ve found all 3 products good. (I know Coloplast is Convatec) But thanks for letting me butt in. I try to avoid commenting on something that is really none of my business, but when it comes to a subject like the "Govt not subsidising Ostomy supplies" I can’t help myself. Cheers, John H(I)  Reply without the junk harmon…@tpg.nospamcom.au "NewzDesk" <InTheP…@none.com

wrote in message

news:3d0f62b1$1_3@spamkiller.newsgroups.com… – Hide quoted text — Show quoted text -> "harmonica" <harmonica…@hotmail.zzn.com

wrote in message

> news:3d0f0e0c@dnews.tpgi.com.au… > > Good luck to you both! > > I hope as many people as possible support your action to finally get the > > ostomy products you need subsidised by your Government. > > To have Q-Tips and several other mundane items listed alongside Ostomy > > products is a blistering insult! > > John (I) > Thanks for your support, John.  This actually affects ostomates worldwide. > As far as I know, except for Dansac and Eakin, all other major ostomy supply

manufacturers are in the US.  Most of the ostomy supplies used internationally are the same ones we use here.  What you wear in Australia comes from the US – where there are no quality controls appropriate to our appliances/supplies/accessories – due to the FDA classification. Your Convatec, Hollister, NuHope, and so on, are manufactured in the US

and

are in the same category as the Q-Tips.  Convatec services A to V.

Argentina

to Vietnam. Equipment failures and injuries to stoma and skin that occur around the world are a result of FDA classification here in the US. The manufacturers are not accountable. They run their own show. Countries who

do

subsidize ostomy products are paying the US manufacturers for these products. Speaking of suppliers/distributors: FWIW, Convatec is the distributor for Eakin seals in the US and various other countries. Australia uses Omnigon

as

it’s distributor for Eakin. As long as Eakin products continue to be produced in Ireland by the same company we’re safe.  If it ever changes hands and gets to the US manufacturers for control and production we’ll

lose

the high quality.  IMO, the products would be altered to reduce costs to manufacturers and our costs would increase. More importantly we’d lose the highest quality product available to ostomates and wound care patients. NewzDesk addyahoodotcom2reply

Response:

On Tue, 18 Jun 2002 09:41:10 -0700, "NewzDesk" <InTheP…@none.com

wrote:

Thanks for your support, John.  This actually affects ostomates worldwide. As far as I know, except for Dansac and Eakin, all other major ostomy supply manufacturers are in the US.

Braun?  Welland?  Clinimed?

Most of the ostomy supplies used internationally are the same ones we use here.  What you wear in Australia comes from the US – where there are no quality controls appropriate to our appliances/supplies/accessories – due to the FDA classification.

What I wear in Spain, although nominally the same (Braun Biotrol) is subtly different from the product I received in the UK.  The *perfect* bag would be somewhere between the two.

Speaking of suppliers/distributors: FWIW, Convatec is the distributor for Eakin seals in the US and various other countries. Australia uses Omnigon as it’s distributor for Eakin. As long as Eakin products continue to be produced in Ireland by the same company we’re safe.

Agreed.  Eakin specially ship their seals to me, as they have no Spanish agent.  Could you see a major player doing that? As an aside, for we non-US citizens, could somebody explain how Medicare works?  I understand the general idea, but not why some people get it and others don’t, and why it’s considered a last resort. — Bill http://billnot.com

Response:

Subject: Re: To ALL Persons Getting Their Supplies-PART II From: "PcolaPhil" flaretph…@earthlink.net

PcolaPhil: Why don’t you ask the UOA why the directive of their 1999 Board of Directors and the last House of Delegates has not been implemented. We would all be interested in their response. The directive: Investigate the FDA classification of ostomy equipment.

Response:

Ignore my previous John.  I shot from the hip without thinking. My foot tastes horrible. PcolaPhil  When I read about the evils of drinking, I gave up reading.                                               – -Henny Youngman "harmonica" <harmonica…@hotmail.zzn.com

wrote in message

news:3d0f0e0c@dnews.tpgi.com.au… | Good luck to you both! | | I hope as many people as possible support your action to finally get the | ostomy products you need subsidised by your Government. | | To have Q-Tips and several other mundane items listed alongside Ostomy | products is a blistering insult! | John (I) | | | To have Ostomy products itemised alongside | "NewzDesk" <InTheP…@none.com

wrote in message

| news:3d0ecad7_1@spamkiller.newsgroups.com… |

Part II

|

|

4. con’t

|

|

Manufacturers do not want ostomy supplies’ coverage dropped

because like | any |

medication that goes from a prescription form to

over-the-counter, the | price |

can drop as much as 80%.  I don’t think I will see a box of

wafer for $3 | in |

my lifetime.  Those of you who use catheters, what about

$1/doz? Who’s | more |

powerful? The insurance industry or manufacturers of ostomy

supplies? |

|

The pharmaceutical corps that most of the supply

manufacturers are related |

to are NOT going to spend a dime or time against their

blood-brothers, the |

Insurance Industry, in order to save the ostomy supply

business as it | exists |

today. For one thing, ‘IT’S NOT COST EFFECTIVE". Insurance

and pharm |

industries will continue profits in the billions without the

supply |

manufacturers.  The "supply industry" may well be

restructured one day – | by |

their own "family".

|

|

I probably need to tone this down a little but am in a hurry.

These are | my |

opinions. I believe in capitalism too, I am not opposed to

anyone and |

everyone making enormous profits and becoming billionaires.

What I don’t |

like is the continued unconscionable price-gouging of these

industries. |

Their utter disregard for consumers and patients.

|

|

It’s situations just like this "revision" of the

reimbursement charges for |

Medicare that are quietly happening, one by one, ten by ten,

state by | state, |

agency by agency, getting by most of the population

unnoticed.  And for | the |

most part, unchallenged. UOA fought and worked tirelessly to

obtain the |

increase in the monthly amounts allowed in the first place.

It went into |

effect  April 1 2001. This is June 2002.

|

|

Ostomates are at the bottom of the barrel. Still the

invisible population. |

|

As PcolaPhil said, "This is one of those occasions when we

might indeed be |

the masters of our fate.  What we do or don’t do can make the

difference. |

My e-mail is in…" Mine will be too.

|

|

NewzDesk

|

addyahoodotcom4reply

|

|

| | |

Response:

How about you supporting the effort that is really a UOA effort. Don’t be scared off by the Medicare title.  What Medicare does, the big insurance companies will eventually ape.  Get Mad!  You have congressmen to talk to… PcolaPhil  When I read about the evils of drinking, I gave up reading.                                               – -Henny Youngman "harmonica" <harmonica…@hotmail.zzn.com

wrote in message

news:3d0f0e0c@dnews.tpgi.com.au… | Good luck to you both! | | I hope as many people as possible support your action to finally get the | ostomy products you need subsidised by your Government. | | To have Q-Tips and several other mundane items listed alongside Ostomy | products is a blistering insult! | John (I) | | | To have Ostomy products itemised alongside | "NewzDesk" <InTheP…@none.com

wrote in message

| news:3d0ecad7_1@spamkiller.newsgroups.com… |

Part II

|

|

4. con’t

|

|

Manufacturers do not want ostomy supplies’ coverage dropped

because like | any |

medication that goes from a prescription form to

over-the-counter, the | price |

can drop as much as 80%.  I don’t think I will see a box of

wafer for $3 | in |

my lifetime.  Those of you who use catheters, what about

$1/doz? Who’s | more |

powerful? The insurance industry or manufacturers of ostomy

supplies? |

|

The pharmaceutical corps that most of the supply

manufacturers are related |

to are NOT going to spend a dime or time against their

blood-brothers, the |

Insurance Industry, in order to save the ostomy supply

business as it | exists |

today. For one thing, ‘IT’S NOT COST EFFECTIVE". Insurance

and pharm |

industries will continue profits in the billions without the

supply |

manufacturers.  The "supply industry" may well be

restructured one day – | by |

their own "family".

|

|

I probably need to tone this down a little but am in a hurry.

These are | my |

opinions. I believe in capitalism too, I am not opposed to

anyone and |

everyone making enormous profits and becoming billionaires.

What I don’t |

like is the continued unconscionable price-gouging of these

industries. |

Their utter disregard for consumers and patients.

|

|

It’s situations just like this "revision" of the

reimbursement charges for |

Medicare that are quietly happening, one by one, ten by ten,

state by | state, |

agency by agency, getting by most of the population

unnoticed.  And for | the |

most part, unchallenged. UOA fought and worked tirelessly to

obtain the |

increase in the monthly amounts allowed in the first place.

It went into |

effect  April 1 2001. This is June 2002.

|

|

Ostomates are at the bottom of the barrel. Still the

invisible population. |

|

As PcolaPhil said, "This is one of those occasions when we

might indeed be |

the masters of our fate.  What we do or don’t do can make the

difference. |

My e-mail is in…" Mine will be too.

|

|

NewzDesk

|

addyahoodotcom4reply

|

|

| | |

Response:

Part II 4. con’t Manufacturers do not want ostomy supplies’ coverage dropped because like any medication that goes from a prescription form to over-the-counter, the price can drop as much as 80%.  I don’t think I will see a box of wafer for $3 in my lifetime.  Those of you who use catheters, what about $1/doz? Who’s more powerful? The insurance industry or manufacturers of ostomy supplies? The pharmaceutical corps that most of the supply manufacturers are related to are NOT going to spend a dime or time against their blood-brothers, the Insurance Industry, in order to save the ostomy supply business as it exists today. For one thing, ‘IT’S NOT COST EFFECTIVE". Insurance and pharm industries will continue profits in the billions without the supply manufacturers.  The "supply industry" may well be restructured one day – by their own "family". I probably need to tone this down a little but am in a hurry.  These are my opinions. I believe in capitalism too, I am not opposed to anyone and everyone making enormous profits and becoming billionaires.  What I don’t like is the continued unconscionable price-gouging of these industries. Their utter disregard for consumers and patients. It’s situations just like this "revision" of the reimbursement charges for Medicare that are quietly happening, one by one, ten by ten, state by state, agency by agency, getting by most of the population unnoticed.  And for the most part, unchallenged. UOA fought and worked tirelessly to obtain the increase in the monthly amounts allowed in the first place. It went into effect  April 1 2001. This is June 2002. Ostomates are at the bottom of the barrel. Still the invisible population. As PcolaPhil said, "This is one of those occasions when we might indeed be the masters of our fate.  What we do or don’t do can make the difference. My e-mail is in…" Mine will be too. NewzDesk addyahoodotcom4reply

Response:

"harmonica" <harmonica…@hotmail.zzn.com

wrote in message

news:3d0f0e0c@dnews.tpgi.com.au…

Good luck to you both! I hope as many people as possible support your action to finally get the ostomy products you need subsidised by your Government. To have Q-Tips and several other mundane items listed alongside Ostomy products is a blistering insult! John (I)

Thanks for your support, John.  This actually affects ostomates worldwide. As far as I know, except for Dansac and Eakin, all other major ostomy supply manufacturers are in the US.  Most of the ostomy supplies used internationally are the same ones we use here.  What you wear in Australia comes from the US – where there are no quality controls appropriate to our appliances/supplies/accessories – due to the FDA classification. Your Convatec, Hollister, NuHope, and so on, are manufactured in the US and are in the same category as the Q-Tips.  Convatec services A to V. Argentina to Vietnam. Equipment failures and injuries to stoma and skin that occur around the world are a result of FDA classification here in the US. The manufacturers are not accountable. They run their own show. Countries who do subsidize ostomy products are paying the US manufacturers for these products. Speaking of suppliers/distributors: FWIW, Convatec is the distributor for Eakin seals in the US and various other countries. Australia uses Omnigon as it’s distributor for Eakin. As long as Eakin products continue to be produced in Ireland by the same company we’re safe.  If it ever changes hands and gets to the US manufacturers for control and production we’ll lose the high quality.  IMO, the products would be altered to reduce costs to manufacturers and our costs would increase. More importantly we’d lose the highest quality product available to ostomates and wound care patients. NewzDesk addyahoodotcom2reply

Response:

Subject: Re: To ALL Persons Getting Their Supplies-PART II From: "harmonica" harmonica…@hotmail.zzn.com To have Q-Tips and several other mundane items listed alongside Ostomy products is a blistering insult! John (I)

What are you and other ostomates going to do about it. UOA  Board of Directors, in 1999, directed their Advocacy/Govt. Affairs committee to investigate the FDA classification. Nothing has been done.

Response:

Good luck to you both! I hope as many people as possible support your action to finally get the ostomy products you need subsidised by your Government. To have Q-Tips and several other mundane items listed alongside Ostomy products is a blistering insult! John (I) To have Ostomy products itemised alongside "NewzDesk" <InTheP…@none.com

wrote in message

news:3d0ecad7_1@spamkiller.newsgroups.com… – Hide quoted text — Show quoted text -

Part II 4. con’t Manufacturers do not want ostomy supplies’ coverage dropped because like

any

medication that goes from a prescription form to over-the-counter, the

price

can drop as much as 80%.  I don’t think I will see a box of wafer for $3

in

my lifetime.  Those of you who use catheters, what about $1/doz? Who’s

more

powerful? The insurance industry or manufacturers of ostomy supplies? The pharmaceutical corps that most of the supply manufacturers are related to are NOT going to spend a dime or time against their blood-brothers, the Insurance Industry, in order to save the ostomy supply business as it

exists

today. For one thing, ‘IT’S NOT COST EFFECTIVE". Insurance and pharm industries will continue profits in the billions without the supply manufacturers.  The "supply industry" may well be restructured one day –

by

their own "family". I probably need to tone this down a little but am in a hurry.  These are

my

opinions. I believe in capitalism too, I am not opposed to anyone and everyone making enormous profits and becoming billionaires.  What I don’t like is the continued unconscionable price-gouging of these industries. Their utter disregard for consumers and patients. It’s situations just like this "revision" of the reimbursement charges for Medicare that are quietly happening, one by one, ten by ten, state by

state,

agency by agency, getting by most of the population unnoticed.  And for

the

most part, unchallenged. UOA fought and worked tirelessly to obtain the increase in the monthly amounts allowed in the first place. It went into effect  April 1 2001. This is June 2002. Ostomates are at the bottom of the barrel. Still the invisible population. As PcolaPhil said, "This is one of those occasions when we might indeed be the masters of our fate.  What we do or don’t do can make the difference. My e-mail is in…" Mine will be too. NewzDesk addyahoodotcom4reply

Response:

"PcolaPhil" <flaretph…@earthlink.net

wrote in message

news:4hxP8.1865$uH2.477@newsread1.prod.itd.earthlink.net…

THIS IS IMPORTANT!!! If you obtain your ostomy supplies thru Medicare, whether you are a member of UOA or not, the information in the article which I have copied and the links therein is for you.  Recent reimbursement changes made are in danger of being reversed!!!

Part I 1.  This affects ALL ostomates, yes, jpouchers too. Medicare or not. At some point, all of us in the US are going to have Medicare, unless billgates-wealthy. Every single change (and this is a big one) affects everyone and is NOT only about ostomy supplies and accessories. 2.  Insurance companies, and the employers who are courted by them for Employee Plans, are ever reducing and/or discontinuing benefits. As premiums continue to rise. Medicare is a guideline used by MANY insurance companies/managed care groups and, OF course, straight HMO’s to set rates/fees/charges/prices/allowable coverages. Many "good" insurance plans no longer cover items, ostomy or otherwise, if Medicare does not cover them.  Those on Medicare with a secondary health plan are screwed too. A secondary health plan will NOT pick up costs on items Medicare does not cover. Reducing Medicare coverage for ostomy supplies is great for the insurance industry. In more ways than cutting back on our ostomy supplies/accessories. Remember the costs of these supplies. From catheters to wafers/pouches, etc., it can run a few hundred a month depending on the individual and circumstances. There are Seniors out there on SocSec only. Rent or ostomy supplies? Forget medications or food. If we turn a blind eye to them what’s next for the rest of us? We will all be affected, one way or another. Now or later. 3.  Many insurance companies have dropped coverage of supplies. Many more will follow.  Any ostomate who had a diagnosis of ulcerative colitis, crohn’s, or the other IBD’s that result in an ostomy keeps that diagnosis FOREVER.  Being "cured" by surgery does not remove that diagnosis. It is pre-existing regardless of how many years’ old.  If a jpoucher needs a bandage for a sprained wrist down the line, could they be refused as a result of restricted policies (fill in your own scenario) regarding pre-existing history of UC? This may well be in our future. All of us. This is why I am adamant about issues re the future of ostomates in this continuing downward spiral of healthcare in this country. We are getting lost in the shuffle. Along with millions of others for a variety of reasons. 4. I have no confidence that insurance companies/Medicare will continue to cover ostomy supplies/accessories in the future.  Or us as an IBD-diagnosed population.  WHY would they continue to cover our UNNECESSARY supplies? Yes, this IS part of this issue. The insurance companies have been gearing in this direction for some time.  The FDA classification for ostomy supplies and accessories is in the same class as Q-Tips. Are Q-Tips a medical necessity? Issues of quality control are meaningless NOW. What happens in the future? Continued on next post, Part II NewzDesk

Response:

THIS IS IMPORTANT!!! If you obtain your ostomy supplies thru Medicare, whether you are a member of UOA or not, the information in the article which I have copied and the links therein is for you.  Recent reimbursement changes made are in danger of being reversed!!! UOA needs YOUR help, by June 28 The United Ostomy Association has a very important meeting scheduled on July 1 – we will meet with the officials of the US Centers for Medicare and Medicaid Services (CMS), to discuss their intent to roll back some improvements that just went into effect on April 1st. After many years of inadequate reimbursement by Medicare, the 4/1 changes made it possible for Medicare beneficiaries to get their supplies and pay less from their own pocket. But CMS, who initially approved the changes, now thinks they should be revised again, and it will definitely have a negative financial impact on senior Americans. YOU CAN HELP, before July 1, by visiting the UOA Advocacy Page (see link below) and using the information there to contact your elected officials. Simply select and read the "alert" about contacting CMS, enter your zip code to go to a list of your Congressmen, select both Senators and your Rep and hit "compose", then review the pre-worded letter – feel free to make any changes to personalize it. Follow the rest of the directions to either email it or print it out to mail through the USPS. A copy of your email will go automatically to CMS Administrator Tom Scully. Every American who relies on Medicare for their supplies will be affected by what you do to help – and I know they will be grateful for your support. Linda Aukett, Chair UOA Government Affairs Committee advoc…@uoa.org UOA Advocacy Page: http://www.uoa.org/advocacy/ —————————————————————– ————— This is one of those occasions when we might indeed be the masters of our fate.  What we do or don’t do can make the difference.  My e-mail is in… PcolaPhil  The Daily Dose "I told the doctor I broke my leg in two places. He told me to quit going to those two places."                         — Comedian Henny Youngman

Response:

Got my Biopsy back

Question:

think about it for a couple of days and talks with a few people and get back to me?  That was almost two weeks ago?

Tell him you thought about it too, and are changing doctors. You don’t need this type of doctor  for "possible" crohn’s disease. What else could all these red inflamed area’s of the bowels and colon be

I really would get a second opinion….

Response:

Thanks Donna — Interesting that there is always an exception to every rule. And you are right about the constipation (although that is NOT a problem with me). Heard it can be as bad as the big *D*. Rebecca :-)

– Hide quoted text — Show quoted text – Next, and this is a question for everyone. My understanding is that alternating diarrhea/constipation is more a symptom of IBS than IBD (which is usually diarrhea all the time, or constipation all the time instead of alternating). Am I correct on this? Also — UC almost always presents blood (except in my case of course <G). I think it is a good sign you are not bleeding. Hi Rebecca… My surgeon told me that in RARE cases some people with IBD experience both constipation and diarrhea…. You’re right about the IBS symptoms of alternating diarrhea and constipation….often a doc excludes IBD as a possibility if you have the constipation as well…..which is a big mistake!!!…. Donna

Response:

I’ve never had blood (even at my worst) either (and blood is supposed to be one *proof* of UC). But, I’ve also never had constipation, ever, ever. Rebecca :-)

– Hide quoted text — Show quoted text – I had both when my CD was active, and I NEVER had blood, even at my worst.  Go figure. My surgeon told me that in RARE cases some people with IBD experience both constipation and diarrhea…. You’re right about the IBS symptoms of alternating diarrhea and constipation….often a doc excludes IBD as a possibility if you have the constipation as well…..which is a big mistake!!!…. Donna

Response:

Have you been tested for various infections of the bowel?

Response:

Wow! 50 lbs?! You must feel like a whole different person! As I am sure you know, if you continue to lose weight (weight that you don’t want to lose) — talk to your doc ASAP. Many IBDers have trouble keeping weight on (I am not one of those) and you can get dangerously thin. I hear you about all the different meds — I’d still try and chart everything just to see if there are any patterns. But, then, I am a *charting* kind of person (type A personality all the way). Good luck!!! Rebecca :-)

– Hide quoted text — Show quoted text – x-no-archive: yes Hi: Just a quick suggestion and a couple of comments. First, have your biopsies sent to another lab. I did this with mine (sent them out of state) just to make sure the dx was correct (both labs said UC). Oh — and if the slides still exist from your first set of biopsies, have those sent as well. Next, and this is a question for everyone. My understanding is that alternating diarrhea/constipation is more a symptom of IBS than IBD (which is usually diarrhea all the time, or constipation all the time instead of alternating). Am I correct on this? Also — UC almost always presents blood (except in my case of course <G). I think it is a good sign you are not bleeding. Another thought as I read your comments. Besides the cramps getting worse, now that you are off all your meds have any other symptoms gotten better/worse? Headaches? Joint pain? Gas? Bloating? Stool consistency? Stool color? Cramps? Etc. Etc. If I were you, I’d chart all this everyday and let the doc know. It might help decide what to do next. Also chart foods/drinks/stress/anything else you can think of that causes any trouble. Basically, chart your every move and every feeling for a while and see what patterns emerge <grin. Good luck, getting the proper dx seems to be half the battle in this disease! Oh, and I’d call you doc right away — two weeks is too long to be off all meds and in pain!! Shame on him/her for not getting back to you pronto! Holler if you need a hug. Rebecca :-) Half of my problem is that originally I did have the bleeding etc, Normally I do have the Diarrhea all the time it’s only since this last colonoscopy that it’s been alternating between the big D and the Big C, that and some of my Meds have been changed around for some of my other problems which is another reason why it’s hard for me to keep track of what goes on daily. I have a lot of things wrong with me so it’s hard to tell exactly what is being caused by what disease or disability that I have <G.  The UC or whatever the hell it is I have does seem to be a bit better since I’ve been on the topamax for my FMS but then again as I said now I just don’t eat any more either <G. On the bright side the Topamax has allowed me to lose over 50 lbs since I’ve been on it, another few pounds and I’ll be down to the perfect weight for my height, age and build.  What happens after I reach my perfect weight while still on the Topamax is beyond me?

Response:

I had both when my CD was active, and I NEVER had blood, even at my worst.  Go figure. – Hide quoted text — Show quoted text -My surgeon told me that in RARE cases some people with IBD experience both constipation and diarrhea…. You’re right about the IBS symptoms of alternating diarrhea and constipation….often a doc excludes IBD as a possibility if you have the constipation as well…..which is a big mistake!!!…. Donna

Response:

Next, and this is a question for everyone. My understanding is that alternating diarrhea/constipation is more a symptom of IBS than IBD (which is usually diarrhea all the time, or constipation all the time instead of alternating). Am I correct on this? Also — UC almost always presents blood (except in my case of course <G). I think it is a good sign you are not bleeding.

Hi Rebecca… My surgeon told me that in RARE cases some people with IBD experience both constipation and diarrhea…. You’re right about the IBS symptoms of alternating diarrhea and constipation….often a doc excludes IBD as a possibility if you have the constipation as well…..which is a big mistake!!!…. Donna

Response:

Well when I switched docs in 1995 he sent my biopsies to 3 labs.  2 came back CDand one came back UC and he determined I have pan-colonic CD.  He said one of the CD findings was by someone he considers the top guy in the field here in WA.  So it’s not unusual to have conflicting findings from the lab. – Hide quoted text — Show quoted text -x-no-archive: yes OK if anyone remembers what’s been going on, I had the ct scan a few weeks ago that came back normal then I had the colonoscopy 2 weeks ago.  I’ve had UC for over a year now and been on all kinds of meds with nothing working for me so far.  The only med I’ve not been on has been the High Dose prednisone. Ok so the Biopsy comes back and my doc calls me, he says it comes back and looks exactly like it did last year when I had the colonoscopy, but microscopically it really does not show like it should for colitis, ulcerative colitis, Crohn’s or IB?  In fact he’s not really sure just what it is? I have all the symptoms of all of those but no blood for a long time which is good, but none of the medication has worked on me? So he had me stop everything I was on except the levbid and told me he would think about it for a couple of days and talks with a few people and get back to me?  That was almost two weeks ago? So far I have not heard back from him, the cramps are far worst then before and now I am going back and forth between bought of Diarrhea and Constipation and I only eat once per day 8 times a week but that is mainly because of another medication I’m on for my FMS. SO with all of the experience in this NG of people with these problems what would you guys do? During the colonoscopy the doc found several areas of the red inflamed areas all through my bowels and colon, I saw the pictures and matched them up with pictures on the internet, pick one of the diseases UC, Crohn’s or whatever and they match but according to the biopsies he took they don’t come back as anything specific, but what scares me is he said they came back exactly as they did last year when he said I had UC? What else could all these red inflamed area’s of the bowels and colon be that are giving me severe cramps on the left and right sides, diarrhea and constipation all the time every day every week every month of the year? Could it be I just had an idiot who did the Biopsies at wherever they were sent, most likely the hospital I had the colonoscopy done at?  I am quite sure all of these problem are not nothing.  I am also quite sure I am not ready to live the rest of my life like this without some kind of medication to try and help me and without a name for what I have? Confused?  You bet I am, at least before I had a name for it and I thought we were making some progress by trying and ruling out different medications until we found one that was going to work for me?  Now I am just in limbo again! — I don’t like Google They have no business archiving my articles without my permission!

Response:

Hi: Just a quick suggestion and a couple of comments. First, have your biopsies sent to another lab. I did this with mine (sent them out of state) just to make sure the dx was correct (both labs said UC). Oh — and if the slides still exist from your first set of biopsies, have those sent as well. Next, and this is a question for everyone. My understanding is that alternating diarrhea/constipation is more a symptom of IBS than IBD (which is usually diarrhea all the time, or constipation all the time instead of alternating). Am I correct on this? Also — UC almost always presents blood (except in my case of course <G). I think it is a good sign you are not bleeding. Another thought as I read your comments. Besides the cramps getting worse, now that you are off all your meds have any other symptoms gotten better/worse? Headaches? Joint pain? Gas? Bloating? Stool consistency? Stool color? Cramps? Etc. Etc. If I were you, I’d chart all this everyday and let the doc know. It might help decide what to do next. Also chart foods/drinks/stress/anything else you can think of that causes any trouble. Basically, chart your every move and every feeling for a while and see what patterns emerge <grin. Good luck, getting the proper dx seems to be half the battle in this disease! Oh, and I’d call you doc right away — two weeks is too long to be off all meds and in pain!! Shame on him/her for not getting back to you pronto! Holler if you need a hug. Rebecca :-)

– Hide quoted text — Show quoted text – x-no-archive: yes OK if anyone remembers what’s been going on, I had the ct scan a few weeks ago that came back normal then I had the colonoscopy 2 weeks ago.  I’ve had UC for over a year now and been on all kinds of meds with nothing working for me so far.  The only med I’ve not been on has been the High Dose prednisone. Ok so the Biopsy comes back and my doc calls me, he says it comes back and looks exactly like it did last year when I had the colonoscopy, but microscopically it really does not show like it should for colitis, ulcerative colitis, Crohn’s or IB?  In fact he’s not really sure just what it is? I have all the symptoms of all of those but no blood for a long time which is good, but none of the medication has worked on me? So he had me stop everything I was on except the levbid and told me he would think about it for a couple of days and talks with a few people and get back to me?  That was almost two weeks ago? So far I have not heard back from him, the cramps are far worst then before and now I am going back and forth between bought of Diarrhea and Constipation and I only eat once per day 8 times a week but that is mainly because of another medication I’m on for my FMS. SO with all of the experience in this NG of people with these problems what would you guys do? During the colonoscopy the doc found several areas of the red inflamed areas all through my bowels and colon, I saw the pictures and matched them up with pictures on the internet, pick one of the diseases UC, Crohn’s or whatever and they match but according to the biopsies he took they don’t come back as anything specific, but what scares me is he said they came back exactly as they did last year when he said I had UC? What else could all these red inflamed area’s of the bowels and colon be that are giving me severe cramps on the left and right sides, diarrhea and constipation all the time every day every week every month of the year? Could it be I just had an idiot who did the Biopsies at wherever they were sent, most likely the hospital I had the colonoscopy done at?  I am quite sure all of these problem are not nothing.  I am also quite sure I am not ready to live the rest of my life like this without some kind of medication to try and help me and without a name for what I have? Confused?  You bet I am, at least before I had a name for it and I thought we were making some progress by trying and ruling out different medications until we found one that was going to work for me?  Now I am just in limbo again! — I don’t like Google They have no business archiving my articles without my permission!

Response:

Hi. Confusion is a common feeling with IBD, I have felt it myself many, many times when trying to figure out what is going on. I don’t recall anyone ever telling me they could tell if I had CD based on how it looked under a microscope, although I don’t know about UC or the other varients of IBD. I would make an apointment with the doctor, because if it is getting worse, then it is not getting better. Sounds kind of simple, but that is a good enough reason to try something different. Maybe a second opinion if your doctor does not respond. You have all your medical records, or can have them sent somewhere, so you won’t have to go through all the tests again. Good luck, I hope you get some releif soon. Cliff

– Hide quoted text — Show quoted text – x-no-archive: yes OK if anyone remembers what’s been going on, I had the ct scan a few weeks ago that came back normal then I had the colonoscopy 2 weeks ago.  I’ve had UC for over a year now and been on all kinds of meds with nothing working for me so far.  The only med I’ve not been on has been the High Dose prednisone. Ok so the Biopsy comes back and my doc calls me, he says it comes back and looks exactly like it did last year when I had the colonoscopy, but microscopically it really does not show like it should for colitis, ulcerative colitis, Crohn’s or IB?  In fact he’s not really sure just what it is? I have all the symptoms of all of those but no blood for a long time which is good, but none of the medication has worked on me? So he had me stop everything I was on except the levbid and told me he would think about it for a couple of days and talks with a few people and get back to me?  That was almost two weeks ago? So far I have not heard back from him, the cramps are far worst then before and now I am going back and forth between bought of Diarrhea and Constipation and I only eat once per day 8 times a week but that is mainly because of another medication I’m on for my FMS. SO with all of the experience in this NG of people with these problems what would you guys do? During the colonoscopy the doc found several areas of the red inflamed areas all through my bowels and colon, I saw the pictures and matched them up with pictures on the internet, pick one of the diseases UC, Crohn’s or whatever and they match but according to the biopsies he took they don’t come back as anything specific, but what scares me is he said they came back exactly as they did last year when he said I had UC? What else could all these red inflamed area’s of the bowels and colon be that are giving me severe cramps on the left and right sides, diarrhea and constipation all the time every day every week every month of the year? Could it be I just had an idiot who did the Biopsies at wherever they were sent, most likely the hospital I had the colonoscopy done at?  I am quite sure all of these problem are not nothing.  I am also quite sure I am not ready to live the rest of my life like this without some kind of medication to try and help me and without a name for what I have? Confused?  You bet I am, at least before I had a name for it and I thought we were making some progress by trying and ruling out different medications until we found one that was going to work for me?  Now I am just in limbo again! — I don’t like Google They have no business archiving my articles without my permission!

Response:

Do You Use Androgel?

Question:

I thought he might be a medical professionnal and maybe a caregiver… But no way to tell for sure as long as he doesn’t tell us who he is. I hope he’ll learn to behave and find a more human attitude so he can find his place in this ng. Noella – Hide quoted text — Show quoted text – Like you Susan, I read the post about bone problems- either he’s been on pred or he’s a postmenopausal woman :-0.  Also, there’s just no way anyone’s reading CCFA’s IBD journal unless they have this illness or they’re a medical professional specializing in it. writes: Sue didn’t say.  She just said he did have IBD.  Sorry can’t help more. UM MOM Susan So, does s/he have UC or CD? I guess I missed that post. Rebecca :-) Sue very well put.  And I am glad you cleared up that NA does have IBD. I have asked because it is hard to take advice from someone who hasn’t been in our shoes.  I believe I read the other day that he said something about bone problems or something.  I too feel he is a very bright intelligent person and has some excellent input.  I just wish he would learn to stop the flaming and realize it doesn’t help anyone including himself.  UM MOM Susan That’s right, anyone and everyone is welcome here so long as they follow the (few) ng rules as set forth in the charter. If Fran had no connection at all to IBD, so long as she followed those rules she would be welcome here.  As it is, she is indeed a caregiver: she’s been helping out a very close friend whose little girl has IBD and who isn’t as Usenet savvy as Fran, and this situation while improved is far from resolved. OTOH, even people with IBD (and yes, NA does have IBD) have to follow the rules or they risk instructions being posted on the ng on how to complain to their ISPs. The not flaming rule isn’t applied evenly: on one end of the spectrum, people who come here simply to get their jollies starting flamewars are shown the door pretty quickly, on the other end, people who are long time regulars and slip up once in awhile find their slipups ignored or are mildly admonished, which typically leads to an apology, and all is right with the world again. NA is a rather odd amalgalm of helpful and flamer.  I say rather odd because usually people with IBD who have ‘flaming’ personalities (I await the double entendres on that last phrase!) typically either come to realize that the flaming ruins the giving and receiving of support, and quit it, or decide the ng is ‘no fun’ and go away. This realization usually comes especially quickly to those who appear from their posts, as NA does, to be extremely intelligent.  I *think* what’s going on in NA’s head is that by flaming people who make a lot of errors, or who he views as ‘poseurs’, he’ll be driving them away and improving the signal to noise ratio in the ng. In reality, it’s easy enough to correct people’s mistakes without flaming, and flaming invariably, without exception, degrades the quality of the ng. It’s sad, because NA does often make very positive contributions to the ng, and increasing numbers of people don’t even see them because they block him so as not to see the flames.  And in yet another way in which he’s showing poor judgment, it sure seems from tracing his address and looking at the pattern of posting that he is doing so from work.  At some point he’s going to ’stalk’ someone here who then turns around and posts the name of the place he’s posting from, the exact server he’s posting from, and the names, addresses and phone numbers of 2 people to complain to at that place.  Since there isn’t that much expertise needed, it’s only a matter of time. I want to join Rebecca in thanking everyone for not flaming, and exhorting people to ignore NA by not responding to his flames, or by blocking him if he really bothers you. And now, by popular request, the ng charter: What is Alt.support.crohns-colitis? Alt.support.crohns-colitis was created in early 1994 as a forum where people suffering from ulcerative colitis, Crohn’s Disease, and irritable bowel syndrome can share their everyday struggles with these illnesses, as well as discuss medicines, treatments, surgery, diet, health care providers, related illnesses, and anything else anyone can think of that relates to these diseases.  In other words, this is the online equivalent of a support group, which means that no question is stupid and no condition embarrassing here.  It also means we’re all here to help each other out, so please be nice, be polite, and no flaming. Discussions of all types of medicine- conventional and alternative, Western and Eastern, your Aunt Harriet’s home remedies, whatever- are welcome here; however, any person discussing a potential remedy which he or she also sells must explicitly begin the "Subject" header of their post with the word "AD" or "ADVERTISEMENT" in all caps, regardless of whether or not they profit from such sales.  Spamming is expressly forbidden as violating the rules of netiquette as well as those of this newsgroup. Finally, please keep in mind that no one knows what causes these illnesses, no one’s come up with a cure, and we need all the help we can get.

Response:

Like you Susan, I read the post about bone problems- either he’s been on pred or he’s a postmenopausal woman :-0.  Also, there’s just no way anyone’s reading CCFA’s IBD journal unless they have this illness or they’re a medical professional specializing in it. – Hide quoted text — Show quoted text -Sue didn’t say.  She just said he did have IBD.  Sorry can’t help more.  UM MOM Susan So, does s/he have UC or CD? I guess I missed that post. Rebecca :-) Sue very well put.  And I am glad you cleared up that NA does have IBD. I have asked because it is hard to take advice from someone who hasn’t been in our shoes.  I believe I read the other day that he said something about bone problems or something.  I too feel he is a very bright intelligent person and has some excellent input.  I just wish he would learn to stop the flaming and realize it doesn’t help anyone including himself.  UM MOM Susan That’s right, anyone and everyone is welcome here so long as they follow the (few) ng rules as set forth in the charter. If Fran had no connection at all to IBD, so long as she followed those rules she would be welcome here.  As it is, she is indeed a caregiver: she’s been helping out a very close friend whose little girl has IBD and who isn’t as Usenet savvy as Fran, and this situation while improved is far from resolved. OTOH, even people with IBD (and yes, NA does have IBD) have to follow the rules or they risk instructions being posted on the ng on how to complain to their ISPs. The not flaming rule isn’t applied evenly: on one end of the spectrum, people who come here simply to get their jollies starting flamewars are shown the door pretty quickly, on the other end, people who are long time regulars and slip up once in awhile find their slipups ignored or are mildly admonished, which typically leads to an apology, and all is right with the world again. NA is a rather odd amalgalm of helpful and flamer.  I say rather odd because usually people with IBD who have ‘flaming’ personalities (I await the double entendres on that last phrase!) typically either come to realize that the flaming ruins the giving and receiving of support, and quit it, or decide the ng is ‘no fun’ and go away.  This realization usually comes especially quickly to those who appear from their posts, as NA does, to be extremely intelligent.  I *think* what’s going on in NA’s head is that by flaming people who make a lot of errors, or who he views as ‘poseurs’, he’ll be driving them away and improving the signal to noise ratio in the ng. In reality, it’s easy enough to correct people’s mistakes without flaming, and flaming invariably, without exception, degrades the quality of the ng. It’s sad, because NA does often make very positive contributions to the ng, and increasing numbers of people don’t even see them because they block him so as not to see the flames.  And in yet another way in which he’s showing poor judgment, it sure seems from tracing his address and looking at the pattern of posting that he is doing so from work.  At some point he’s going to ’stalk’ someone here who then turns around and posts the name of the place he’s posting from, the exact server he’s posting from, and the names, addresses and phone numbers of 2 people to complain to at that place.  Since there isn’t that much expertise needed, it’s only a matter of time. I want to join Rebecca in thanking everyone for not flaming, and exhorting people to ignore NA by not responding to his flames, or by blocking him if he really bothers you. And now, by popular request, the ng charter: What is Alt.support.crohns-colitis? Alt.support.crohns-colitis was created in early 1994 as a forum where people suffering from ulcerative colitis, Crohn’s Disease, and irritable bowel syndrome can share their everyday struggles with these illnesses, as well as discuss medicines, treatments, surgery, diet, health care providers, related illnesses, and anything else anyone can think of that relates to these diseases.  In other words, this is the online equivalent of a support group, which means that no question is stupid and no condition embarrassing here.  It also means we’re all here to help each other out, so please be nice, be polite, and no flaming. Discussions of all types of medicine- conventional and alternative, Western and Eastern, your Aunt Harriet’s home remedies, whatever- are welcome here; however, any person discussing a potential remedy which he or she also sells must explicitly begin the "Subject" header of their post with the word "AD" or "ADVERTISEMENT" in all caps, regardless of whether or not they profit from such sales.  Spamming is expressly forbidden as violating the rules of netiquette as well as those of this newsgroup.  Finally, please keep in mind that no one knows what causes these illnesses, no one’s come up with a cure, and we need all the help we can get.

Response:

Sue didn’t say.  She just said he did have IBD.  Sorry can’t help more.  UM MOM Susan

– Hide quoted text — Show quoted text – So, does s/he have UC or CD? I guess I missed that post. Rebecca :-) Sue very well put.  And I am glad you cleared up that NA does have IBD. I have asked because it is hard to take advice from someone who hasn’t been in our shoes.  I believe I read the other day that he said something about bone problems or something.  I too feel he is a very bright intelligent person and has some excellent input.  I just wish he would learn to stop the flaming and realize it doesn’t help anyone including himself.  UM MOM Susan That’s right, anyone and everyone is welcome here so long as they follow the (few) ng rules as set forth in the charter. If Fran had no connection at all to IBD, so long as she followed those rules she would be welcome here.  As it is, she is indeed a caregiver: she’s been helping out a very close friend whose little girl has IBD and who isn’t as Usenet savvy as Fran, and this situation while improved is far from resolved. OTOH, even people with IBD (and yes, NA does have IBD) have to follow the rules or they risk instructions being posted on the ng on how to complain to their ISPs. The not flaming rule isn’t applied evenly: on one end of the spectrum, people who come here simply to get their jollies starting flamewars are shown the door pretty quickly, on the other end, people who are long time regulars and slip up once in awhile find their slipups ignored or are mildly admonished, which typically leads to an apology, and all is right with the world again. NA is a rather odd amalgalm of helpful and flamer.  I say rather odd because usually people with IBD who have ‘flaming’ personalities (I await the double entendres on that last phrase!) typically either come to realize that the flaming ruins the giving and receiving of support, and quit it, or decide the ng is ‘no fun’ and go away.  This realization usually comes especially quickly to those who appear from their posts, as NA does, to be extremely intelligent.  I *think* what’s going on in NA’s head is that by flaming people who make a lot of errors, or who he views as ‘poseurs’, he’ll be driving them away and improving the signal to noise ratio in the ng. In reality, it’s easy enough to correct people’s mistakes without flaming, and flaming invariably, without exception, degrades the quality of the ng. It’s sad, because NA does often make very positive contributions to the ng, and increasing numbers of people don’t even see them because they block him so as not to see the flames.  And in yet another way in which he’s showing poor judgment, it sure seems from tracing his address and looking at the pattern of posting that he is doing so from work.  At some point he’s going to ’stalk’ someone here who then turns around and posts the name of the place he’s posting from, the exact server he’s posting from, and the names, addresses and phone numbers of 2 people to complain to at that place.  Since there isn’t that much expertise needed, it’s only a matter of time. I want to join Rebecca in thanking everyone for not flaming, and exhorting people to ignore NA by not responding to his flames, or by blocking him if he really bothers you. And now, by popular request, the ng charter: What is Alt.support.crohns-colitis? Alt.support.crohns-colitis was created in early 1994 as a forum where people suffering from ulcerative colitis, Crohn’s Disease, and irritable bowel syndrome can share their everyday struggles with these illnesses, as well as discuss medicines, treatments, surgery, diet, health care providers, related illnesses, and anything else anyone can think of that relates to these diseases.  In other words, this is the online equivalent of a support group, which means that no question is stupid and no condition embarrassing here.  It also means we’re all here to help each other out, so please be nice, be polite, and no flaming. Discussions of all types of medicine- conventional and alternative, Western and Eastern, your Aunt Harriet’s home remedies, whatever- are welcome here; however, any person discussing a potential remedy which he or she also sells must explicitly begin the "Subject" header of their post with the word "AD" or "ADVERTISEMENT" in all caps, regardless of whether or not they profit from such sales.  Spamming is expressly forbidden as violating the rules of netiquette as well as those of this newsgroup.  Finally, please keep in mind that no one knows what causes these illnesses, no one’s come up with a cure, and we need all the help we can get.

Response:

So, does s/he have UC or CD? I guess I missed that post. Rebecca :-)

Sue very well put.  And I am glad you cleared up that NA does have IBD.  I have asked because it is hard to take advice from someone who hasn’t been in our shoes.  I believe I read the other day that he said something about bone problems or something.  I too feel he is a very bright intelligent person and has some excellent input.  I just wish he would learn to stop the flaming and realize it doesn’t help anyone including himself.  UM MOM Susan

– Hide quoted text — Show quoted text – That’s right, anyone and everyone is welcome here so long as they follow the (few) ng rules as set forth in the charter. If Fran had no connection at all to IBD, so long as she followed those rules she would be welcome here.  As it is, she is indeed a caregiver: she’s been helping out a very close friend whose little girl has IBD and who isn’t as Usenet savvy as Fran, and this situation while improved is far from resolved. OTOH, even people with IBD (and yes, NA does have IBD) have to follow the rules or they risk instructions being posted on the ng on how to complain to their ISPs. The not flaming rule isn’t applied evenly: on one end of the spectrum, people who come here simply to get their jollies starting flamewars are shown the door pretty quickly, on the other end, people who are long time regulars and slip up once in awhile find their slipups ignored or are mildly admonished, which typically leads to an apology, and all is right with the world again. NA is a rather odd amalgalm of helpful and flamer.  I say rather odd because usually people with IBD who have ‘flaming’ personalities (I await the double entendres on that last phrase!) typically either come to realize that the flaming ruins the giving and receiving of support, and quit it, or decide the ng is ‘no fun’ and go away.  This realization usually comes especially quickly to those who appear from their posts, as NA does, to be extremely intelligent.  I *think* what’s going on in NA’s head is that by flaming people who make a lot of errors, or who he views as ‘poseurs’, he’ll be driving them away and improving the signal to noise ratio in the ng. In reality, it’s easy enough to correct people’s mistakes without flaming, and flaming invariably, without exception, degrades the quality of the ng. It’s sad, because NA does often make very positive contributions to the ng, and increasing numbers of people don’t even see them because they block him so as not to see the flames.  And in yet another way in which he’s showing poor judgment, it sure seems from tracing his address and looking at the pattern of posting that he is doing so from work.  At some point he’s going to ’stalk’ someone here who then turns around and posts the name of the place he’s posting from, the exact server he’s posting from, and the names, addresses and phone numbers of 2 people to complain to at that place.  Since there isn’t that much expertise needed, it’s only a matter of time. I want to join Rebecca in thanking everyone for not flaming, and exhorting people to ignore NA by not responding to his flames, or by blocking him if he really bothers you. And now, by popular request, the ng charter: What is Alt.support.crohns-colitis? Alt.support.crohns-colitis was created in early 1994 as a forum where people suffering from ulcerative colitis, Crohn’s Disease, and irritable bowel syndrome can share their everyday struggles with these illnesses, as well as discuss medicines, treatments, surgery, diet, health care providers, related illnesses, and anything else anyone can think of that relates to these diseases.  In other words, this is the online equivalent of a support group, which means that no question is stupid and no condition embarrassing here.  It also means we’re all here to help each other out, so please be nice, be polite, and no flaming. Discussions of all types of medicine- conventional and alternative, Western and Eastern, your Aunt Harriet’s home remedies, whatever- are welcome here; however, any person discussing a potential remedy which he or she also sells must explicitly begin the "Subject" header of their post with the word "AD" or "ADVERTISEMENT" in all caps, regardless of whether or not they profit from such sales.  Spamming is expressly forbidden as violating the rules of netiquette as well as those of this newsgroup.  Finally, please keep in mind that no one knows what causes these illnesses, no one’s come up with a cure, and we need all the help we can get.

Response:

Sue very well put.  And I am glad you cleared up that NA does have IBD.  I have asked because it is hard to take advice from someone who hasn’t been in our shoes.  I believe I read the other day that he said something about bone problems or something.  I too feel he is a very bright intelligent person and has some excellent input.  I just wish he would learn to stop the flaming and realize it doesn’t help anyone including himself.  UM MOM Susan – Hide quoted text — Show quoted text – That’s right, anyone and everyone is welcome here so long as they follow the (few) ng rules as set forth in the charter. If Fran had no connection at all to IBD, so long as she followed those rules she would be welcome here.  As it is, she is indeed a caregiver: she’s been helping out a very close friend whose little girl has IBD and who isn’t as Usenet savvy as Fran, and this situation while improved is far from resolved. OTOH, even people with IBD (and yes, NA does have IBD) have to follow the rules or they risk instructions being posted on the ng on how to complain to their ISPs. The not flaming rule isn’t applied evenly: on one end of the spectrum, people who come here simply to get their jollies starting flamewars are shown the door pretty quickly, on the other end, people who are long time regulars and slip up once in awhile find their slipups ignored or are mildly admonished, which typically leads to an apology, and all is right with the world again. NA is a rather odd amalgalm of helpful and flamer.  I say rather odd because usually people with IBD who have ‘flaming’ personalities (I await the double entendres on that last phrase!) typically either come to realize that the flaming ruins the giving and receiving of support, and quit it, or decide the ng is ‘no fun’ and go away.  This realization usually comes especially quickly to those who appear from their posts, as NA does, to be extremely intelligent.  I *think* what’s going on in NA’s head is that by flaming people who make a lot of errors, or who he views as ‘poseurs’, he’ll be driving them away and improving the signal to noise ratio in the ng. In reality, it’s easy enough to correct people’s mistakes without flaming, and flaming invariably, without exception, degrades the quality of the ng. It’s sad, because NA does often make very positive contributions to the ng, and increasing numbers of people don’t even see them because they block him so as not to see the flames.  And in yet another way in which he’s showing poor judgment, it sure seems from tracing his address and looking at the pattern of posting that he is doing so from work.  At some point he’s going to ’stalk’ someone here who then turns around and posts the name of the place he’s posting from, the exact server he’s posting from, and the names, addresses and phone numbers of 2 people to complain to at that place.  Since there isn’t that much expertise needed, it’s only a matter of time. I want to join Rebecca in thanking everyone for not flaming, and exhorting people to ignore NA by not responding to his flames, or by blocking him if he really bothers you. And now, by popular request, the ng charter: What is Alt.support.crohns-colitis? Alt.support.crohns-colitis was created in early 1994 as a forum where people suffering from ulcerative colitis, Crohn’s Disease, and irritable bowel syndrome can share their everyday struggles with these illnesses, as well as discuss medicines, treatments, surgery, diet, health care providers, related illnesses, and anything else anyone can think of that relates to these diseases.  In other words, this is the online equivalent of a support group, which means that no question is stupid and no condition embarrassing here.  It also means we’re all here to help each other out, so please be nice, be polite, and no flaming. Discussions of all types of medicine- conventional and alternative, Western and Eastern, your Aunt Harriet’s home remedies, whatever- are welcome here; however, any person discussing a potential remedy which he or she also sells must explicitly begin the "Subject" header of their post with the word "AD" or "ADVERTISEMENT" in all caps, regardless of whether or not they profit from such sales.  Spamming is expressly forbidden as violating the rules of netiquette as well as those of this newsgroup.  Finally, please keep in mind that no one knows what causes these illnesses, no one’s come up with a cure, and we need all the help we can get.

Response:

That’s right, anyone and everyone is welcome here so long as they follow the (few) ng rules as set forth in the charter. If Fran had no connection at all to IBD, so long as she followed those rules she would be welcome here.  As it is, she is indeed a caregiver: she’s been helping out a very close friend whose little girl has IBD and who isn’t as Usenet savvy as Fran, and this situation while improved is far from resolved. OTOH, even people with IBD (and yes, NA does have IBD) have to follow the rules or they risk instructions being posted on the ng on how to complain to their ISPs. The not flaming rule isn’t applied evenly: on one end of the spectrum, people who come here simply to get their jollies starting flamewars are shown the door pretty quickly, on the other end, people who are long time regulars and slip up once in awhile find their slipups ignored or are mildly admonished, which typically leads to an apology, and all is right with the world again. NA is a rather odd amalgalm of helpful and flamer.  I say rather odd because usually people with IBD who have ‘flaming’ personalities (I await the double entendres on that last phrase!) typically either come to realize that the flaming ruins the giving and receiving of support, and quit it, or decide the ng is ‘no fun’ and go away.  This realization usually comes especially quickly to those who appear from their posts, as NA does, to be extremely intelligent.  I *think* what’s going on in NA’s head is that by flaming people who make a lot of errors, or who he views as ‘poseurs’, he’ll be driving them away and improving the signal to noise ratio in the ng. In reality, it’s easy enough to correct people’s mistakes without flaming, and flaming invariably, without exception, degrades the quality of the ng. It’s sad, because NA does often make very positive contributions to the ng, and increasing numbers of people don’t even see them because they block him so as not to see the flames.  And in yet another way in which he’s showing poor judgment, it sure seems from tracing his address and looking at the pattern of posting that he is doing so from work.  At some point he’s going to ’stalk’ someone here who then turns around and posts the name of the place he’s posting from, the exact server he’s posting from, and the names, addresses and phone numbers of 2 people to complain to at that place.  Since there isn’t that much expertise needed, it’s only a matter of time. I want to join Rebecca in thanking everyone for not flaming, and exhorting people to ignore NA by not responding to his flames, or by blocking him if he really bothers you. And now, by popular request, the ng charter: What is Alt.support.crohns-colitis? Alt.support.crohns-colitis was created in early 1994 as a forum where people suffering from ulcerative colitis, Crohn’s Disease, and irritable bowel syndrome can share their everyday struggles with these illnesses, as well as discuss medicines, treatments, surgery, diet, health care providers, related illnesses, and anything else anyone can think of that relates to these diseases.  In other words, this is the online equivalent of a support group, which means that no question is stupid and no condition embarrassing here.  It also means we’re all here to help each other out, so please be nice, be polite, and no flaming. Discussions of all types of medicine- conventional and alternative, Western and Eastern, your Aunt Harriet’s home remedies, whatever- are welcome here; however, any person discussing a potential remedy which he or she also sells must explicitly begin the "Subject" header of their post with the word "AD" or "ADVERTISEMENT" in all caps, regardless of whether or not they profit from such sales.  Spamming is expressly forbidden as violating the rules of netiquette as well as those of this newsgroup.  Finally, please keep in mind that no one knows what causes these illnesses, no one’s come up with a cure, and we need all the help we can get.

Response:

NA, I can explain very easily why Fran is very much an asset to this group. First, she came here to get knowledge about IBD to help Arrianne and Beth. That is true love and friendship.  Second, Fran is a mother to her own children and though they don’t have IBD thank goodness there are medical and emotional needs for all children and she manages to tend to her own family and still find time to try to learn to help another family.  And finally, she helps those of us when we are sick to not give up and reminds us why.  I think all these things are a big asset and valuable contribution to this group and that is why she is my friend.  I don’t think I can say it any plainer.  Love and compassion is a powerful tool for everyone.  UM MOM Susan

– Hide quoted text — Show quoted text – Ignore her. She has no experience with IBD. Why this healthy person is so entranced with the topic of inflamed intestines is a mystery. If this is something that would interest the group (and somehow I doubt it, given its name, but I’m prepared to be proven wrong) then all discussion should be kept within the group. — Fran

Response:

Thanks to everyone for not turning this into a flame war — just two observations: 1. As far as I know (and please correct me if I am wrong, Sue) there is no where in the ng charter that says ONLY people with IBD may post here. In fact, some of the most knowledgeable, wonderful, supportive people we have here are caregivers of people with IBD. Fran would fall into that category. 2. As far as I remember (and anyone can correct me on this one) NA has never once said that he/she has any form of IBD (or is a caregiver). So, if we were to apply his logic to himself — then we should just "ignore" him/her. Rebecca :-)

– Hide quoted text — Show quoted text – Ignore her. She has no experience with IBD. Why this healthy person is so entranced with the topic of inflamed intestines is a mystery. If this is something that would interest the group (and somehow I doubt it, given its name, but I’m prepared to be proven wrong) then all discussion should be kept within the group. — Fran

Response:

megabite said… If you use Androgel, I would like to chat with you. Contact me with your email address. Thanks. If this is something that would interest the group (and somehow I doubt it, given its name, but I’m prepared to be proven wrong) then all discussion should be kept within the group. — Fran

Actually, megabite has posted a couple of times asking the ng about androgel and if memory serves me received no replies, so maybe s/he feels more feedback would occur via email.

Response:

http://www.androgel.com/  This is some really nasty stuff.  I did a search on it and this a steroid abused by athletes to make themselves bigger and stronger.  Here is just one of the links.  UM MOM Susan, who would never touch this stuff.

– Hide quoted text — Show quoted text – If you use Androgel, I would like to chat with you. Contact me with your email address. Thanks.

Response:

Interesting. Never heard of it.         Elizabeth – Hide quoted text — Show quoted text – http://www.androgel.com/  This is some really nasty stuff.  I did a search on it and this a steroid abused by athletes to make themselves bigger and stronger.  Here is just one of the links.  UM MOM Susan, who would never touch this stuff. If you use Androgel, I would like to chat with you. Contact me with your email address. Thanks.

Response:

Ignore her. She has no experience with IBD. Why this healthy person is so entranced with the topic of inflamed intestines is a mystery.   – Hide quoted text — Show quoted text – If this is something that would interest the group (and somehow I doubt it, given its name, but I’m prepared to be proven wrong) then all discussion should be kept within the group. — Fran

Response:

I don’t need you to tell me whose posts to read.         Elizabeth – Hide quoted text — Show quoted text – Ignore her. She has no experience with IBD. Why this healthy person is so entranced with the topic of inflamed intestines is a mystery. If this is something that would interest the group (and somehow I doubt it, given its name, but I’m prepared to be proven wrong) then all discussion should be kept within the group. — Fran

Response:

If you use Androgel, I would like to chat with you. Contact me with your email address. Thanks.

Response:

Hey Fran, There is no need to act like a jackass. I’ve had Crohn’s for a long time. I’m going to start using this product to help counteract problems that I have had due to Crohn’s and the use of medications that I have used. I posted here for help not insults. Have a nice day.

– Hide quoted text — Show quoted text – megabite said… If you use Androgel, I would like to chat with you. Contact me with your email address. Thanks. If this is something that would interest the group (and somehow I doubt it, given its name, but I’m prepared to be proven wrong) then all discussion should be kept within the group. — Fran

Response:

is there a FAQ page

Question:

Thanks Howard, my ISP was all messed up for about 5 days and I’m just catching up on the (way over 1000) posts.  Here’s the Welcome to asc-c message for y’all: Welcome to alt.support.crohns-colitis!  Here are some important links to get you started, and the newsgroup charter to give you an idea of what we’re all about here: Want the FAQs, plus lots of other useful information about IBD and this newsgroup?  Check out these websites http://qurlyjoe.bu.edu/cduchome.html   AND http://ascc.healingwell.com Confused ’cause you’ve got mail from Gail?  Check out http://ascc.healingwell.com/info/gailfaq.htm And now (drumroll please) our charter: What is Alt.support.crohns-colitis? Alt.support.crohns-colitis was created in early 1994 as a forum where people suffering from ulcerative colitis, Crohn’s Disease, and irritable bowel syndrome can share their everyday struggles with these illnesses, as well as discuss medicines, treatments, surgery, diet, health care providers, related illnesses, and anything else anyone can think of that relates to these diseases.  In other words, this is the online equivalent of a support group, which means that no question is stupid and no condition embarrassing here.  It also means we’re all here to help each other out, so please be nice, be polite, and no flaming. Discussions of all types of medicine- conventional and alternative, Western and Eastern, your Aunt Harriet’s home remedies, whatever- are welcome here; however, any person discussing a potential remedy which he or she also sells must explicitly begin the "Subject" header of their post with the word "AD" or "ADVERTISEMENT" in all caps, regardless of whether or not they profit from such sales.  Spamming is expressly forbidden as violating the rules of netiquette as well as those of this newsgroup.  Finally, please keep in mind that no one knows what causes these illnesses, no one’s come up with a cure, and we need all the help we can get.

Response:

THANK YOU THANK YOU THANK YOU!!!!!! I really appreciated the following line! <G Ceresse  I know that I need all the help I can get! – Hide quoted text — Show quoted text –  Finally, please keep in mind that no one knows what causes these illnesses, no one’s come up with a cure, and we need all the help we can get.

Response:

Thanks for the link. I have been using the NG for a few years it seems but I just read a newbies post and thought .. I bet there are answers out there as to etiquette and standards that I assume we all know. now I will know. thanks again lisa – Hide quoted text — Show quoted text – lisa The FAQ’s are posted here on the newsgroup every couple weeks, but they are also on several web pages. Bill Robertson’s Crohn’s Disease and Ulcerative Colitis Page http://qurlyjoe.bu.edu/cduchome.html Steve H’s alt.support.crohns-colitis on the web. http://ascc.healingwell.com/ The first has the FAQ’s for IBD (inflammatory bowel disease) The second has them as well as some info about ASCC. Howard I was just wondering if there is a FAQ page or guide lines for this newsgroup? Just wondering lisa

Response:

lisa The FAQ’s are posted here on the newsgroup every couple weeks, but they are also on several web pages. Bill Robertson’s Crohn’s Disease and Ulcerative Colitis Page http://qurlyjoe.bu.edu/cduchome.html Steve H’s alt.support.crohns-colitis on the web. http://ascc.healingwell.com/ The first has the FAQ’s for IBD (inflammatory bowel disease) The second has them as well as some info about ASCC. Howard – Hide quoted text — Show quoted text – I was just wondering if there is a FAQ page or guide lines for this newsgroup? Just wondering lisa

Response:

Thanks Howard, I knew you wouldn’t let me down! :)  mgbio – Hide quoted text — Show quoted text – lisa The FAQ’s are posted here on the newsgroup every couple weeks, but they are also on several web pages. Bill Robertson’s Crohn’s Disease and Ulcerative Colitis Page http://qurlyjoe.bu.edu/cduchome.html Steve H’s alt.support.crohns-colitis on the web. http://ascc.healingwell.com/ The first has the FAQ’s for IBD (inflammatory bowel disease) The second has them as well as some info about ASCC. Howard I was just wondering if there is a FAQ page or guide lines for this newsgroup? Just wondering lisa

Response:

I was just wondering if there is a FAQ page or guide lines for this newsgroup? Just wondering lisa

Response:

There is a FAQ, Sue should post it as soon as she sees your message. It is a standard FAQ, no flaming, any commercial posts needs AD in the header, no bad language as we do have children that visit. etc. Mike I was just wondering if there is a FAQ page or guide lines for this newsgroup? Just wondering lisa

Please Visit www.ibdcure.com and sign the petition for an IBD postage stamp. All opinions expressed are mine unless otherwise noted. Leah’s Body Sugaring Recipe Remove unwanted hair http://www.for-romance.com/sugar "those that can be offended, will be" … Pastor Don

Response:

Lisa, Yes, there is a FAQ.  I believe Steve has it on his web page (sorry, I can’t recall the URL but Howard should know it) and Sue posts it regularly.  You may want to search the archives using Google to find it. :)  mgbio – Hide quoted text — Show quoted text – I was just wondering if there is a FAQ page or guide lines for this newsgroup? Just wondering lisa

Response: