I was diagnosed with Crohn's about a year ago after I had my gall bladder removed and the surgeon said he could see the what looked like Crohn's. This made sense to me because I always had abdominal pain but thought that was just how I was. I am now 36 but can remember symptoms back to 23. My main symptom has always been abdominal pain and occasional diarrhea. So for the last year I have been on budesonide but it seems to have stopped working. I had bloody stools for a few days so the GI switched me to Pentasa and Prednisone. I also had a CT that showed a narrowing or stricture in the terminal ileum. Not sure if they are the same thing? Not sure how bad it is I don't have my appointment with him until November 13th. Ever since I started the Prednisone I have been so bloated that I feel like my stomach is going to pop. A couple of nights ago I felt like the food was just sitting in my stomach not going anywhere and I finally had to vomit to get relief. Was that a blockage? or does prednisone cause that? Since then I have been worried to eat. Should I keep eating or switch to liquids? This is the first time I have actually vomited from this disease. Any advice would be appreciated.