Has anyone tried Low-Dose Naltrexone (LDN)?

Three months on LDN for ME/CFS. Honestly can't tell if it's doing much. The first few weeks were rough — more fatigue, more malaise — then it levelled out. I'm at 3mg now. Some days I think there's a slight improvement in my cognitive function but I could be wrong. Still taking it.

↑ 18 · all posts are anonymous by default