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Just Diagnosed

Right after you are diagnosed with ulcerative colitis, it FOR SURE is an awful time. With doctor appointments nearly every day, and medications needing to be picked up from the store and countless visits to the bathroom each day…it’s not a fun time. But like other parts of UC, the diagnosis period is part of the process to getting things under control and the stories below detail first hand experiences of what it is like.

Anyone Else a Newbie in Their UC Diagnosis?

Hi, I’m Erica and I have UC. I’m 23 years old and have been diagnosed for about 7 months. First off, let me offer a forewarning; I am currently on the “prednisone makeover” from my first flare up, so if I either ramble with something along the lines of pointless rage or exaggerated frustration, you all know why! (apologies in advance!).

New to UC – And Now Horrible Anxiety

I am new to this disease/site and while it has been very helpful it also has given me horrible anxiety. I don’t have most of the symptoms most people have and that scares me that my anxiety is that bad now I can’t even imagine what it will be when this gets worse. I have basically been reading non stop in multiple forums and that only proceeds to freak me out more.