C
Chap
Guest
Hi,
I just joined the forum and posted a short intro earlier. I have mild CD and would like clarification on what a flare-up is, and how it differs from the agonizing bouts when I eat the wrong thing, get a small intestine blockage, and have to go to the ER for morphine and prednisone.
I always called these trips to the ER "flare-ups" but now I'm understanding that the flare is more when the auto-immune aspect of Crohn's kicks in, which simply makes me *vulnerable* to bowel blockage. I have no clue when this happens - I don't have bloody stools or diarrhea EVER (well, so far ... ;-)
Have I got this approximately correct? If I knew when I was "flaring", I could be extra cautious about what I eat during those times.
Thanks,
Chap
I just joined the forum and posted a short intro earlier. I have mild CD and would like clarification on what a flare-up is, and how it differs from the agonizing bouts when I eat the wrong thing, get a small intestine blockage, and have to go to the ER for morphine and prednisone.
I always called these trips to the ER "flare-ups" but now I'm understanding that the flare is more when the auto-immune aspect of Crohn's kicks in, which simply makes me *vulnerable* to bowel blockage. I have no clue when this happens - I don't have bloody stools or diarrhea EVER (well, so far ... ;-)
Have I got this approximately correct? If I knew when I was "flaring", I could be extra cautious about what I eat during those times.
Thanks,
Chap