I saw my gastroenterologist today. I always remind myself to try to remember everything she says so I can write it down here, but I’m not very good at it.
She said my colonoscopy back in July looked very good. I think she said she took a bunch of biopsies, which surprised me, because I didn’t think they had. In previous colonoscopies, there were times where it hurt, and I figured that was because they were taking a biopsy, but during my last colonoscopy, it didn’t hurt at all. She said something about the left side, I think maybe there was inflammation there. But I think she basically said it looks like there wasn’t any active Crohn’s.
I had my second colonoscopy on Monday. My first colonoscopy was a little more than two years ago. That post is one of the most popular posts on my blog, so I figured I’d write about this one too.
First off, I’m twenty-two years old, and I’m in my fourth year of university. I live in southern Ontario, Canada, and I was diagnosed with Crohn’s disease in December 2009, after a terrible year where I was very sick, and the doctors didn’t know what was wrong with me. I went to the hospital in December (thinking I had appendicitis) and had some tests done. They found that I had a perforated bowel, so I had a bowel resection. I had my first colonoscopy in February 2010. I wasn’t on any medication until June 2011, when I took Prednisone for a few months. That was a miracle, and I have been quite well ever since. This colonoscopy was just a precaution to make sure we aren’t sitting ducks for something bad to happen.