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Pouchitis
IgG4 pouchitis and Pepto Bismol effects?Go ![]() | New ![]() | Find ![]() | Notify ![]() | Tools ![]() | Reply ![]() | |
i have been reading more and more people having success against pouchitis when using Pepto Bismol . For those of us who are IgG4 positive(antibiotic resistant), would this help us out any? "It's always somethin'..." Diagnosed UC 1996 Surgery due to Low Grade Dysplasia Step 1- April 4th, 2008,8 week stay due to ecoli infection Step 2 - Aug.8th 2008,2 week stay due to c-diff infection Had surgery at The Cleveland Clinic in Cleveland,OH. NOV.30th. 2009- 1st.Bowel Obstruction/NG Tube. diagnosed IgG4 positive 4/2011, ongoing cuffitis 4/6/12 diagnosed with fistula now. | |||
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Hi there, I have not yet been confirmed positive for IgG4, but I have suspected I am for years now. I read a medical abstract a few years ago by Dr. Shen about this "new" autoimmune disease and have been researching it ever since. None of the doctors in my area have any idea about a J-Pouch, much less the more specialized IgG4. I NEVER thought something as simple as Pepto Bismol would help. I had been on every biological and combination-everything. I continue to suffer from cuffitis and pouchitis, and basically have since 2 weeks after my pouch. But, after my mother insisting I give it a whirl, I was so surprised that PB actually helped, and not by a small amount, but more than any drug I had yet to try!! I have scoured the research for any adverse reactions to long time use of PB and haven't found any. I would say to try it. Not much to lose...right? I use two tablets (or you can do chewables or liquids-another great thing about it) every 3-4 hours. I hope it works for you too. | ||||
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I take Pepto Bismol chewable tablets between antibiotic doses if I start feeling irritated. I feel it helps. DJBHusky UC - 1972 as a 9 year old Takedown 1992 Chronic Pouchitis Onset 1995 Still J Pouching 2012 | ||||
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I too am IgG4 positive - not being treated specifically for it, but taking canasa for cuffitis and tindamax for fistula, feeling pretty well. However, a few weeks ago I started with the more frequent, small bms., getting up more at night, accidents, inflammatory feelings - started getting a little freaked out - but I restarted the PB and am doing well once again. Once in the am, once before bed seems to do the trick for me. I absolutely think it's worth a try, and can't hurt, far as I'm aware. You may want to send your dr. a note, letting him know that you're giving it a shot. | ||||
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The pepto worked amazingly for my IGG4 Pouchitis, gave me my life back. It worked for about 6 months, but quit. I've tried several times since, and it doesn't seem to work anymore. Well worth a try though, a very cheap and safe treatment! | ||||
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michelb how much were you taking at a time ..maybe noy enough or you needed to up it..i am using in between my antibiotics that are not working as well when i end one and start anotther(i rotate antibiotic) i take 6 at a time...usually amounting to two times in the day beween the antibiotic.. but if you take no antibiotics increase your pb higher.see if it helps rebe Rebecca | ||||
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my son had mild pouchitis for the first year and a half post takedown - he's been taking 2 pepto a day, 2 Align & 2 fiber pills (one in the am and one in the pm). He's been healthy and symptom free for over a year (knock on wood) son diagnosed with UC 2006 (age 6) colectomy & jpouch surgery 7/08 (age 8) takedown surgery 11/08 (age 9) do great now - healthy, growing normal obnoxious | ||||
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Rebecca, I was taking 8 a day, 2 at a time. I was told 10 was the limit I should take. I'll try to up it and see what happens, as I'm not on any other antibiotics. | ||||
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IgG4 pouchitis and Pepto Bismol effects?
