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Possible UC flare

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My doctors decided that I was doing well enough post-transplant (2 years now) that I could finally stop taking the Prednisone. So they had me reduce my dose from 5mg to 2.5mg. Well everything was going just fine for the first two weeks but then my bowels stareted acting up. At first I thought that I had just caught the stomach flu that my sister and her whole family had but it has been 2 weeks and it is not getting any better. Infact on Wedneday it got so bad I called my coordinator and he thought maybe I was having a UC flare because of the decrease in the Prednisone. He put me back on the 5mg dose and I was feeling better on Thursday but worst again on Friday. Satuarday was a good day and today is another bad one. Even though I have had UC for over 16 years I have only had the one flare up that gave me my diagnosis so I'm not sure what to think of this. Is this how a flare-up normally works or does this mean that the Prednisone is working and I am starting to

improve? I'm suppose to be in class all next week for my new job and I'm concerned that this isn't under control yet. What do the rest of you do to get your UC flare-ups back under control? I would really appreciate an advise you guys have. Thanks, Pat (CA) UC 1991, PSC 1999, TX 2005

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5 mg of prednisone may not be enough to control a UC flare up. Are you on

any other meds for UC? I think you should see the GI doc.

-Marie

> I'm suppose to be in class all next week for my new job and I'm

>concerned that this isn't under control yet. What do the rest of you do to

>get your UC flare-ups back under control? I would really appreciate an

>advise you guys have.

>

> Thanks,

>

> Pat (CA) UC 1991, PSC 1999, TX 2005

>

>

>---------------------------------

>Fussy? Opinionated? Impossible to please? Perfect. Join Yahoo!'s user

>panel and lay it on us.

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