I thought I was in a UC flair for 6 months that would simply not abate...minor bleeding, spasms after a BM, pain, mushy stool at the end of a BM etc etc; BUT as some of you may remember my colonoscopy and biopsies came back with no IBD present! So it must be IBS and just knowing that helps me feel better and makes it much easier on me knowing that it's NOT my UC but IBS....the bleeding appears to be coming from an old fissure or internal hemmie.
I wonder how many here are thinking their stubborn flairs are IBD when in fact it may not be at all?
Hope this helps some here : ).
7 Pentasa per day (4/3)
Corti Foam p.m. 2X per week
Probiotics, Bowel Soother, Fish Oil, Calcium, Multi Vitamin and Melatonin
Trying to reduce sugar in my diet but cannot tolerate artificial sweetners
I excersice daily
Did I happen to mention I HATE this disease!!!
Post Edited (bbc) : 11/22/2008 8:52:40 PM (GMT-7)