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    chronic inflammation of J-pouch
    avatar
    sim59 posted:
    was just informed that, after a pouchoscopy, my J-pouch is in a state of chronic inflammation. I've had my pouch since 1995, no major issues other than one or 2 bouts of pouchitis. current doctor is recommending an ongoing course of 6-MP to help manage what he's calling ulcerative colitis around the pouch.

    has anyone else had this issue, or can tell me more about their involvement with 6-MP? I recall taking it orally when i was first diagnosed with UC back in the mid 1980's (when it was first introduced and experimental), and then need to monitor WBC and kidney functions via regular bloodword.

    Thanks in advance!
    Reply
     
    avatar
    miserable_sob responded:
    Welcome to the club. I've been stuck with a j-pouch since 1988. Pouchitis and all that crap is part of the territory. About the only thing I can do at times to make my miserable pouch more tolerable is diet or starve myself. 6-MP is new to me. I've pretty much had it with trying drug after drug only to learn you can't defeat the laws of physics. If I had it my way, I'd gladly live with my diseased colon again. I actually miss it now.
     
    avatar
    hannahleigh89 responded:
    I have a j-pouch but mine is fairly new. I got it in 2010. I also have Crohn's disease though so my case is a little different. I still have chronic inflammatory problems because of the Crohn's, and I receive an infusion every 28 days to deal with that. I can't take 6-MP so I don't have much information to offer you about it. As far as I know, the drug hasn't changed any in the vast number of years it's been available as a treatment. They do have to do regular blood work to check your counts and your liver function, primarily. Do you have any specific questions about it?


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