Will a scheduled colonoscopy cause a relapse of C-Diff?
Currently 3 weeks recovery from C-Diff after taking vancomycin . I have two questions.
I am scheduled for a routine colonoscopy in November (5 years since last colonoscopy). That will only be 2 months of recovery time from C-Diff. Will the colonoscopy create a relapse of C-Diff? Should I wait to have the colonoscopy since this is a routine 5 year check?
Second question is I am due for a tetanus shot (10 years since last one) Can I get the tetanus shot or will it create a relapse of C-Diff?
I do not want a relapse of C-Diff and I am only 3 weeks into recovery!
Interested in more discussions like this? Go to the Digestive Health Support Group.
@subie Hi there please see my message where I added your comment to a discussion. I wanted to ask if you are having symptoms of C Diff or if you have been diagnosed?
Hi there, I trust you are well. Which lactobacillus Acidophilus did you use? Can you add a photo of it?
Here you go, I ordered it thru Amazon
Thank you so much, appreciate it.
My hubby suffered with c-diff, and his story is quite different. He was diagnosed with Ulcerative colitis last year September. He was put on prednisone and asacol and did really well until March this year,2021. He was feeling a bit of gastritis so we went to the Dr who put him on antibiotics - after taking the antibiotics he flared and the Dr put him on steroids again, after tapering the steroids he would flare again, even though his diet remained the same. The Dr would put him back on steroids and he would flare again. Since march this year, he flared every time they tapered him off steroids. So in total, he flared 7 times. Eventually got so bad , he ended up in hospital. He was tested straight away with c - diff being positive. They treated him in hosp for this and then tested again out of hospital which the results came back positive again, only this time making him extremely sick almost felt like he was flaring. So the Dr put him back on steroids treating it as a flare even thou he did not have full blown flare symptoms. He finished vancomycin for the 2nd time and was re-tested. Thankfully the c -diff was negative. His inflammation was also the lowest its ever been since last year. I pray for everyone going through such horrible diseases. Btw, the previous dr did not test my hubby for c-diff while having numerous flares. Thank god, the dr on duty at the time in hospital did otherwise he would've kept going on steroids thinking it was a flare yet it was c-diff that was present for months. Love to all who are suffering, there is always light at the end of the tunnel.
I contracted C-diff after taking Clyndamycin for a dental issue. It was horrible! I truly thought I was not going to make it and neither did my husband. It has taken months to recover thoroughly. I am normally an active person who exercises 6 days a week and tries to stay healthy. This set me back immensely. I was weak for quite a while. Gradually I've improved to the point where my life has returned to "my normal". I also have a "tortuous intestine" (more intestine than needed for a person my size), which has caused me grief and constipation all my life. And actually, through this site, and sharing, I found Prunelax that has helped me more than I can say. I would never want C-diff again but I'm grateful for finding this site. When I was recovering I took pro-biotics for two months along with Miralax, (which did nothing) stool softener, etc. Nothing worked like the Prunelax. I still make sure I'm getting the proper fiber, water intake, and I am taking magnesium but I plan on dropping that when I finish the bottle. It's always a learning process and adjustments need to be made that work best for you as an individual. But as far as recovering from C- diff it took me 9 months to almost get back to the real me. I have lost 10 pounds that I can't seem to gain back and that puzzles me but I'm doing well. I hope that everyone finds what works for them. I know it can be scary and very frustrating to go through this. And initially I was just trying to survive so I understand the fear. Best wishes to all! Merry Christmas! Jacque
Oh my goodness. Terrible. How did you get rid of the C. Diff? Flagyl, Vancomycin, Deficid? Any of these work for you?
I just read here that Mayo Dr. told someone that she will always test positive for C-diff. Is this true? I just tested positive again on a stool sample after finishing Vanco a week later. From reading here, Dificid is the best to try so I just told my Dr. to prescribe it. My co-payment is $50 and the meds cost $7000 for 2 wk supply. That is so unheard of...
After my husband suffered from C-diff for six months, his gastroenterologist prescribed cholestyramine which is actually a cholesterol lowering drug. None of the antibiotics helped but cholestyramine stabilized his gut.
I am on the same drug for chronic diarrhea. It got so bad I felt I could not leave my house. I have never had c-diff and although I was diagnosed with Crohns 50+ years ago, I have been on no medicine and healthy. My problem was the diarrhea from having all but 9 inches of my colon removed 50 years ago. Cholestrymine keeps it to a manageable level. BTW it was an internist, not a gastro that prescribed it and saved me.