Have rC-diff - 7th time in less than 2 1/2 yrs. Tried all antibiotics (dificid, Rifaximin, etc.) for C-diff, plus human monoclonal antibody infusion two times (Bezlotoxumab). Vancomycin is only one that works, but only for 3 - 4 months.
Researching FMT, but have reservations. Is there anyone who has had FMT who is willing to share
after-effects, success/failure rate, and which procedure was used?
Thank you, Elaine

I feel your pain and concerns. I have had cdiff 3 times this year and twice before that. The doctors are working on getting me a pill form for the fecal micro transplant. Ask your doctor about Vowst. I don’t like the idea of what the cure is but I will do what I need to do to stop cdiff. I will let you know if I can get it and how it went. Look up Vowst on the internet. There is lots of information on it.

Thank you SO much, Janet, for sharing that info. The hospital in CO at which my Dr. practices has not (yet) approved the pill form, but has just approved Rebyota.

So sorry that you, too, have been suffering with recurrent, debilitating bouts. My heart goes out to you.

Would very much appreciate hearing about your outcome.

In the past, has your Dr. recommended any probiotic to take? Or any special diet to follow?

I'm currently on pulse & taper of Vancomycin, which only works for a few months.

Thanks for responding.
All the best,
Elaine

Oh, I know exactly what you mean. C-diff controls every aspect of our life, and having to isolate does not help our mood.

Hoping you have a good Gastroenterologist.

I'm new to this discussion, but feel the connectivity to others who understand.

Do your own research, too, to find what procedure you'd be comfortable with. Mayo Clinic seems to have fact-based answers.

Wishing you success in your search.

I feel your pain! I had c-diff 3 times in 2023 and had it twice prior to that. Did the long term vancomycin three times My doctor finally got me approved for Vowst. It’s a fecal micro transplant in pill form. I took it the last of December 2023 and have been c-diff free since then. I would talk to your doctor about it. Hope that helps.

I JUST FINISHED THE FECAL TRANSPLANT, VOWST AND WHILE IT LOWERED MY BMS, THE CDIFF ODOR IS LIKE ALL OVER ME, AND IM REAL ANAL ABOUT CLEANLINESS, I KNOW I DEFINITELY STILL HAVE IT, I WAS WONDERING IF YOU HAD SUCH A REACTION. GOOD LUCK TO YOU. EVERYONE WITH THIS HORRRIBLE CONDITION YOU ARE IN MY PRAYERS.

Has anyone been treated with Vowst