This disease really stinks! I am so angry right now, but not for me. My friend who lived with severe UC for many years finally had a colostomy and she looked stupendous. She got her life back. I was so happy for her and it gave me a lift of extra hope.
Now she is in the hospital with a new diagnosis of crohns in her terminal ileum/anus.
I just need to vent about how much I hate this darn disease for her. It's just not fair to get so far and be pushed backwards. I am hoping she will meet the criteria for one of the newer meds or the stem cell trial to get her back in shape quickly. I just don't know what they will do for her with no large intestine.