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ME/CFS

🥄 Quick readanonymous

Has anyone tried Low-Dose Naltrexone (LDN)?

No effect for me after six months at various doses. Disappointing. My immunologist wasn't surprised — she said response rates in ME seem quite variable. Moving on to trying mestinon next.

ldnme-cfstreatment

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Has anyone tried Low-Dose Naltrexone (LDN)? — Spoons · ME/CFS