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My chiro recommended I look into low dose naltrexone for auto-immune/pouchitis, has anyone tried this? He has patients with MS, RA, & UC that are doing really with it. My PCP called him about it & decided she did not want to prescribe it, but I was considering bringing it up to my GI if this next round of Flagyl & Canasa doesn't do the trick...

Anyone with experience?!?!

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Pulled this from an internet article. Sounds to me like a drug with few side effects. A low dose is needed to heal inflamed mucosa. May be worth trying and thanks for passing the info along for others. Amazing how a chiro can suggest something your gi may have never thought to.

Naltrexone. Originally developed to help treat heroin addiction, lower doses of naltrexone have shown a range of remarkable immunological activities. A placebo-controlled study on the use of low-dose naltrexone (4.5 mg per day at bedtime) suggested that the drug could resolve mucosal inflammation and induce clinical remission in patients with moderate-to-severe Crohn’s disease (Smith 2011). This confirms one earlier uncontrolled study of low-dose naltrexone’s efficacy for Crohn’s disease (Smith 2007). Naltrexone appears to relieve inflammatory bowel disease in part by decreasing expression of proinflammatory cytokines and promoting tissue repair (Matters 2008). At low dosages, the drug may cause drowsiness, but other side effects are uncommon.
J
pouchmonkey - look at healingwell.com - there are numerous posts re. naltrexone experiences there, particularly with Crohn's patients.

I've wanted to try it, but none of my "mainstream" docs would prescribe it. I don't know why they are so resistant, as it appears there's very little to no harm in trying it. I haven't pursued other means of getting a scrip (alternative doctors) yet. Please keep us posted if you try.
n/a
My chiro recommended it specifically because he has other pt's who have used it for auto-immune issues & have done extremely well with it. I have read the online info that notes that it is used for opioid addiction, but that's at 50mg, not the 4.5 mg dose. The pt's he has that have been using it have MS, UC, & Crohn's. My GI (who I have not spoken with yet about LDN, I wanted to finish out my cycle of Flagyl & Canasa first) pretty well told me that pouchitis, or mine specifically in rectal inflammation, can basically be just like UC, so in theory, if the LDN works for UC, could it not work for pouchitis? If anyone runs across someone with personal experience, please let us all know!
pouchmonkey

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