Hi, I'm 19, had what I thought was just Irritable Bowel Syndrome since I was about 10, would always have a bit of tummy trouble after eating certain foods. Then after it getting worse and worse around December 2009 when I was 17, I went to my GP and he had no idea what it could be. He first thought it was an ulcer, so did H.pylori testing. After that we discovered small tender nodes by my iliac lymph area, so he thought maybe ovarian cancer so I had a very uncomfortable ultrasound up to my ovaries, found nothing. By this point I was very frustrated and starting to throw up 2 times a day at least, became lactose intolerant and could not handle protein. Severe stomach cramping and diarrhea when I ate anything. Finally my GP decided it would be smart to send me to a Gastroenterologist, who was in Vancouver. This was a costly flight to go there often. I thank him so much though, for finally figuring it out. I underwent a colonoscopy, and he found moderate Crohn's disease. This all happened right after I had finished losing 60 pounds, barely made it through finals, provincials and graduation. We tried high doses of prednisone, which almost made things worse, then we tried imuran, and after that did not work I was set to receive Remicade (Infliximab). I am currently on 5 boxes every 6 weeks, but I still get symptoms in the week before the next infusion. It was a long year and a half struggle to get where I am now. Recently suffering through what I believe is a flare-up, which would happen to be right before finals for University.