- Joined
- Aug 3, 2010
- Messages
- 1
I was finally diagnosed with Crohn's in 1994 after years of being told I had "Chronic Fatigue Syndrome" following a terrible bout of Glandular Fever which wiped out one whole year of school. Initially I had just awful recurring mouth ulcers and extreme tiredness and was told I had oral Crohn's with no bowel involvement. Over the years I have developed bowel issues - nowhere near as bad as other sufferers - but still bad enough to be debilitating on some days. My worst problems these days are mouth ulcers, sore throats, awful and constant sinus headaches, painful and stiff joints in my hands, feet, knees and back, and the worst of all, tiredness. I have two daughters (the first I conceived when I was on Imuran and Prednisone) and it is sometimes so hard to get out of bed to get them to school.