Thanks everyone so much for your responses, I love this forum, just knowing there are people out there who understand makes it so much easier to cope. I do try really hard to avoid to make UC an...
During my last flare, I really believed that my husband was supportive and understanding. This was the first major one since being married. During an argument today, he raised (because he isn't...
Hi, if you do choose to go down the medication route for this, be careful what you take. I had joint pain before my last flare, and my GP put me on Diclofenac, which I have since heard is not good...
Hi Memmie, although I have not tried to receive benefits for UC, when my work referred me to Occupational Health, the consultant wrote in the report that the 'Disability Discrimination Act' applies...
I feel so bad for moaning, as I know most people reading this are suffering right now with their UC. My UC seems to be under control.... but just feel so bad. Although I am feeling ok, I regularly...
Thanks hippimom, as you say, with chronic illness, nothing is easy...doctors seems to blame everything on the UC! Sometimes its just good to offload dont you think! I will make sure I talk all of my...
Hi, I have ulcerative colitis, and usually just look at the posts there, but for the past six months or so (since recovering from my last flare of UC) I have been exhausted. I have no energy,...