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@lkirnbauer

I had 18” of my Sigmoid Colon removed due to severe diverticulitis back in April of 2022. For years I suffered with on and off issues of diverticulitis and was put on antibiotics along with Flagyl (which is an awful medication that made me nauseous). I had my usual colonoscopy’s and then more frequent ones because my gastroenterologist was removing polyps almost every time, though benign. Finally, my gastroenterologist recommended that I have a resection due to narrowing of my colon and pooping was becoming a problem. I now can eat seeds without a problem and have been more regular with bowel movements. I would begin a regimen of really good pro and prebiotics. They will help with bowel movements and digestion. They will also help your gut with gut flora. Antibiotics kill that off, so be cautious how many of those you’re taking and your doctor should be aware of that. They really are just a band aide for what’s really going on in your gut. Since I had my colon resection, I got Covid in December of that same year, 2022. I lost my taste and smell and still don’t have it back. It’s been awful. Going on 1 year and 8 months soon without tasting or smelling much of anything. The only constant smell I have is my coffee grounds in the morning…I can’t taste anything but salty, sweet or sour. I’ve had 4 Stellate Ganglion Block injections with only a slight improvement. I am running out of things to try to regain it. If anyone reading this has a helpful suggestion, I would be happy to hear it. Good luck on your health journey.

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Replies to "I had 18” of my Sigmoid Colon removed due to severe diverticulitis back in April of..."

Hi,
Thank you for sharing your experience.

Curious, what symptoms were you experiencing with diverticulitis? And how often did it come back? Did you also have IBS or SIBO for years prior to your diverticulitis? Also, what age did it occur?

My symptoms are also IBS type symptoms which I’ve had for years with suspected SIBO. Also my CT scans are negative for diverticulitis. My doc says 53 is young to have diverticulitis. And diarrhea started my onset from my taking long term Paxlovid for LC so more likely not diverticulitis.

I also find it significant that Rifaximin helped me tremendously with everything even beyond gut symptoms such as brain fog, energy levels, decreased PVC’s, improved allergies and no more hypoglycemic feelings that weren’t hypoglycemia. This to me points to gut infections causing my LC issues as well as my long term IBS being a precursor. I could be wrong, only time will tell. But…

Rifaximin has been shown to improve gut flora when taken cyclically. Also, doxycycline has been shown to improve symptoms without full systemic treatment. Here’s an interesting article https://patientresearchcovid19.com/hypothesis-matrix-metalloproteinase-inhibition-with-low-dose-doxycycline-in-long-covid-and-me-cfs-pghj-issue1-may2023/
Here’s a good article on Rifaximin helping down regulate bacterial infections:
https://www.mayoclinicproceedings.org/article/S0025-6196(15)00350-X/fulltext
Rifaximin for IBS, a meta analysis: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10558962/

When you had diverticulitis, what were your precursors and symptoms? Did you try Rifaximin? If so, did it help?

Also how long between episodes of diverticulitis did you have?