I posted this last night under a thread already started in the Ostomy section about Barbie Butt, then realized I should put it in a more general category because it might be overlooked otherwise.
How's this for irony? My biggest fear about having perm ileo surgery has been the potential for picking up infection in the hospital. I finally have a date set to go in a few weeks and, guess what. . . I found out last nigth that I have C Dif! Never had it before and I'm glad we caught it before I went into the hospital, but I am also very disappointed. I started vancomycin 250 mg 4x/day for two weeks and then possibly continuing with a taper. My GI recommended a probtioic, which I already take, but I also plan to take saccharomyces boulardi while I'm on the antibiotic. Sounds like I might need to postpone surgery.
It's weird, though, because I feel really good and have gained weight and have been excited to move forward with the surgery. The only way the C Dif was discovered was when I had a scope and my GI saw some unfamiliar dots mixed in with the ulcerations in my pouch, so he had it checked.
My first response to my GI was asking to do fecal transplant. He adamantly refused and said that that was only for cases when nothing else worked. . .
Does anyone have experience with C Difficile and/or vancomycin, including how they both relate to surgery? Any suggestions?
Thank you!
How's this for irony? My biggest fear about having perm ileo surgery has been the potential for picking up infection in the hospital. I finally have a date set to go in a few weeks and, guess what. . . I found out last nigth that I have C Dif! Never had it before and I'm glad we caught it before I went into the hospital, but I am also very disappointed. I started vancomycin 250 mg 4x/day for two weeks and then possibly continuing with a taper. My GI recommended a probtioic, which I already take, but I also plan to take saccharomyces boulardi while I'm on the antibiotic. Sounds like I might need to postpone surgery.
It's weird, though, because I feel really good and have gained weight and have been excited to move forward with the surgery. The only way the C Dif was discovered was when I had a scope and my GI saw some unfamiliar dots mixed in with the ulcerations in my pouch, so he had it checked.
My first response to my GI was asking to do fecal transplant. He adamantly refused and said that that was only for cases when nothing else worked. . .
Does anyone have experience with C Difficile and/or vancomycin, including how they both relate to surgery? Any suggestions?
Thank you!