Permanent SIBO due to removal of ileocecal valve
Is there anyone who has no cure options for SIBO due to the removal of the ileocecal valve? If so, how do you minimize possible long term damage to your intestinal tract? Do you find that digestive enzymes, L-Glutamine, Enteragam or any natural supplements aid in a healthier immune system? if so,
please pass along your best advice. Thanks.
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I found him through the referral my Family Nurse Practitioner put in when she couldn't figure out what was wrong with me. I had so many blood and stool tests with no finding to explain my chronic diarrhea and feeling unwell everyday.
I am in an HMO and on medicare advantage plan. I cannot self direct my care. Just by luck I had my consult with a gastroenterologist who understands SIBO/ SIFO in post hemicolectomy surgery with removal of the ileocecal valve.
My doctor also said it will be life long. I have had this for several years so I believe him.
I was on Cipro and Metronidazole and now on Augmentin.
I had an emergency right hemicolectomy and ileectomy in 2016 from a cecal volvulus. It's been a rough ride. I too had problems with chronic SIBO. My GI dr did a hydrogen breath test and it was sky high. He put me on several weeks on xifaxan,(rifaximin) and I did great. But, it always came back after a few weeks. Finally he put me on xifaxan 3x daily indefinitely. I had incredible insurance that paid 100% of the cost. Two years ago I was able to get the dosage down to twice a day and am still doing well although I still have a lot of irregularity flareups but I just live with that. Now, I am on Medicare. It is a tier 5 drug which is the most expensive. We got the best drug plan we could find in order to get this drug covered although it will still be expensive until we meet the catastrophic coverage amount. Xifaxan honestly has allowed me to have a better quality of life overall. I can't imagine what it would be like if I was forced to go off. I suffered with IBS since I was a child — always had intestinal problems and now I know that I had a bowel deformity (rotated cecum) that wasn't detected until I obstructed, I'm pretty sure my dr prescribed it for IBS since it is approved for that. Without the IV there's just no way to keep bacteria out of the small intestine. I wish all of us who have had to have this surgery would get a special rate for this crazy insane cost medicine!
I suffered the same history as you. Lifelong bowel problems that plagued me until a volvulus caused me to have a right hemicolectomy with removal of the ileocecal valve in 2015. My quality of life deteriorated and I became more and more ill. Chronic diarrhea, abdominal pain, bone pain, muscle weakness and ternderness, and brain fog. In the last 6 months I have had so much blood work with nothing showing up positive. Finally my PCP referred me to a gastroenterologist that read my surgery history and labs and colitis on CT and said you have bacterial overgrowth due to your hemicolectomy with ileocecal valve removal. I have been on 3 different antibiotics. When I am on them I get better but when the course of antibiotic is finished the diarrhea returns.
I just met my gastroenterologist last week. I see him in 4 weeks to determine what course to take from there. He said patients with SIBO usually remain on treatment the rest of their lives.
Do you get monthly b12 injections?
I hope all of of here who have had an ileectomy and cecum removal are getting monthly (or more often) b12 Injections. Our bodies are no longer able to absorb b12 because the only place it can be absorbed is through the cecum. B12 deficiency can major problems.
I take super B Complex, B levels consistently low
It is medically necessary for b12 injections for those of us with no cecum or ileum. It's shocking how many doctors don't understand how dire and necessary these injections are, you can take as high of mg you want of b12 orally but your body has no way to absorb it. Please talk to your dr about this!
Thank you. When I see him March 2nd this will be on my list of questions.
It's good to hear of another GI dr, besides my own, that understands that chronic SIBO is a real thing for those of us with no ileocecal valve.
I had multiple intestinal surgeries for adhesions due to complications from Gastro bypass. I tack injections b12 weekly , vit d 50,000 and iron infusion annually (fereheme) my illiocecal valve , appendix and gallbladder all removed. The illiocecal valve and surrounding small and large intestine that absorbs those vitamins have been removed