Well, first they tried IV steroids which also didn't do anything so I got started on Remicade as an inpatient. In retrospect, I think that I was probably mismanaged when I was diagnosed (couldn't complete the scope due to inflammatory narrowing but only put on pentasa) and a really poor advocate for myself. I didn't want to be an annoying patient so I never called my doctor when I was feeling worse. Plus, I got zero education and assumed that feeling horrible was part of the crohns that was inevitable. No way to know, but I've always felt that if I had been treated more aggressively at diagnosis, maybe I could have avoided that whole stretch.