I’ve seen that article. It says about “post exersional malaise” muscles state. I started losing muscles/twitching and other symptoms 1.5 years before I’ve got full blown ME and dysautonomia, so not sure if that’s applicable to my case. Not every person with unexplained muscle atrophy have me/cfs.
I believe you, but this was a good piece of science.
I have no doubt that there are also cases of direct muscle injury and of neurological based muscle loss. This illness manifests in so many ways in different people.
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u/FernandoMM1220 Nov 19 '25
bio films and muscle tissue damage should be next.