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Has anyone else seen the new Rapamycin trial for ME/CFS? It's giving me a bit of hope.

By November 15, 2025 - 2:25am

I've been housebound with ME/CFS for years and have tried everything with little success. I just stumbled upon this article about a clinical trial where weekly Rapamycin significantly improved symptoms for some patients. It's only an early trial, but it's the first thing that has made me feel hopeful in a long time. I know it's not a cure, but it feels like a real lead for the first time. What does everyone think?

I found the summary of the trial findings here.

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