Hi, I saw this and just thought I would chime in. I'm 27 and had UC
for 6 years, it got to the point where I decided surgery was the best
option and I am very happy with the results, not only do I not take
any medication now, I finally have control back over my life. Most
people who have the j-pouch surgery for UC always say they wish they
had done it sooner, I am now one of those, but feel it was the right
time for me, I needed to be ready to make that decision and while in
hindsight I would have done it sooner, I'm glad I did not wait any
longer. I tried all the alternative and traditional meds and while
they helped it is so much better now. j-pouch.org is a good source
for informtion about the surgery and keep in mind it is a support
group for people that are having problems with their surgery, most
people don't go there when they are doing just fine, myself included.
Surgery has a finality to it, there is no going back, and to me it
means finally no more UC and never going back to having it again!
hi all, my name is terry, i have recently been diagnosed with colitis. don't know the specifics of what kind. i also have autoimmune vasculitis, called...
HI Terry Welcome to the group..You will find folks on here that care and more than willing to answer any questions that you have to the best of their...
niteowl618@...
Jul 29, 2002 2:31 am
Hi! My name is Samantha and I'm a 17 year old female living in Australia. About 3 weeks ago I noticed a change in my bowel movements and started to bleed and...
Welcome to the group, Samantha! I was just like you a year and a half ago. I never used to be sick aside from the occasional cold and maybe flu. Then all of a...
Hi Samantha, Welcome to the group. My name is Amy, I am 26, and I live in Melbourne. Feel free to email me with any questions you have. I was diagnosed almost...
Hey, My name is Rachel and I am 22. I just got Crohns Colitis last thursday.. very depressing for me. My family never had it. I feel I am the only one in the...
... I ... always ... on ... I'd ... answer ... sick ... my ... like ... now. ... Hello, my name is Rene and I was diagnossed with chrons disease oct 2005. It...
Welcome Samantha, First of all, feel free to ask whatever you want. I'm from Brazil and I was diagnosed with Crohn's Disease three years ago, when I was 21....
Roberto Soares
rfirmeza@...
May 28, 2003 9:55 pm
Hi, I am 36 and was diagnosed with UC about 7 months ago. I was on Asacol for the past 7 months but it didn't stop me from having 3 flare ups in seven months...
I do go to the health food store a lot when I am not in a flare up. I am on Asulphazine which is like prednisone but long term with no side affects. I also...
Hello there all. My name is Steph and I have just been diagnosed with UC in the last few months. It has been tough for me because I already have another...
Hey I'm Rachel.. and nice to meet you online.. ha. and I just found out I have Crohns Colitis last thursday... and sad that i have that diease not a good...
Hi, I saw this and just thought I would chime in. I'm 27 and had UC for 6 years, it got to the point where I decided surgery was the best option and I am very...
Hi Steph, I'm from Indiana, too. I was diagnosed with UC in March 2003. Right now, I'm on 3 Asacols 3 times a day, doc wants to start reducing, but I freaked...
Lanette, Well the doc took me off the canasa because I a barely having any rectal bleeding and that is what it was for. I think I am doing ok, but today as a...
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