What the hell is life Disabled, They/them pronouns

Former hcw with Myalgic Encephalomyelitis aka ‘the living death’ aka ME/CFS x16 yrs LandBack AbolishICE 🍉 “Like a bird in the tree, the prisoners must be fre

*318ppm #introvert #longcovid #mecfs Kulturpessimistin, Untergangsprophetin, Nölerin und Nörglerin, empörte Berufskritikerin.

Disabled, former paralegal posting into the void about covid, climate, and collapse. Still masking. Probably in Denver, Seattle, or Johnson City, TN. Fascists,

NIE WIEDER muß heißen, wir schützen auch andere vor einem WIEDER! 🇺🇦 Twixxer-handle: @FellaJS

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

Surviving MyalgicE aka ME/CFS & AAG to tell the story, pwME & advocate w/ a JD. Into MEdical, Social, Climate Justice & Arts. ME-dical apolide, Human Neutrino,

begrudgingly online for chronic illness research & disability justice community. living meaningfully & unapologetically as a hermit against my will.

Explainer video production: https://clausernst.com/en/ Moderate Long Covid since "mild" SARS-CoV-2 infection in Jan. 2021

Living with ME/CFS since 1983. An advocate since my diagnosis in 1988.

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.