LongCovid Leftism (the normal, boring kind)

I occasionally try to explain and comment on ME research, or even contribute to it. And I advocate for more and better research.

Interested in research into ME/CFS/MECFS, FND and related conditions. https://medium.com/@cfs_research

News and information about interventional trials for Long Covid, ME/CFS, POTS, and other post-viral illnesses. Message or tag me if you’re in a trial or otherwi

NSFW therian.COVID maxxer.owen.30.auDHD.cPTSD.2xdepression.LC.mayosapien. cheese brained ramblings of a tired trans dragon man. hoard: deer mice anticapitalist

95% of posts on #MyalgicEncephalomyelitis, #LongCovid or #chronicillness. With ME/CFS 37 years, severe ME 32 years. @IrishMECFSAssoc trustee 29 years 26 publ

Irish Myalgic Encephalomyelitis/Chronic Fatigue Syndrome Association-for Information, Support & Research NB: Posts ≠ advice. Registered Charity RCN 20100254.