Hello to everyone. I am so thankful to have found this forum. I started with symptoms of crohn's when I was 13, but wasn't diagnosed until I was 21, when I was hospitalized with severe, constant back pain for over a year. I went to every doctor imaginable (including GI) who could not find anything amiss. Some suggested psychiatric help. Finally, I went to an orthopedic surgeon who hospitalized me (5 weeks) and was detemined to find out what was wrong and they finally discovered a huge retroperitoneal abcess. At 29 I had a resection of the terminal ileum and cecum, which had ruptured before the surgery. My husband was told they didn't expect me to live because the peritonitis was so severe and I was septic. But I pulled through (another 5 weeks in the hospital) and have been fairly stable with about 4-6 flare-ups a year. I'm still in the bathroom 8-10 times a day but this has been my life for so long that it is my normal. Recently I've been having more flare-ups and feeling lousy. My doctor put me on 6-MP with no good results--I think I feel worse. I have numerous times where I have to rush to find the nearest bathroom--as many of you know--the WORST feeling. Anyway, I will be trying Humira but am also on Celexa and was wondering if anyone also on Celexa found their symptoms of Crohn's to become worse while taking it. Hope to correspond with many of you on this site in the future!