Philosophy graduate | former science event organiser | former performance artist | ‘former’ and ‘ex’ at most of everything due to #MEcfs

Severe ME patient currently on a 10% battery, the gas goes out more than I do. I also compile ME/CFS Awareness videos. https://linktr.ee/abrokenbattery

#MECFS post-viral #longhauler | ally of #LongCOVID | quoter of @mecfsquotes | previously, 🚵🏼‍♂️ 🏂 🏃🏻🏕️ 📖

ME secondary to Covid vaccination. pro vax/vax injured. Zero tolerance for personal abuse. Do unto others as you would have others do unto you.

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

One of #MillionsMissing since 2002 #MEcfs Diagnose 2021 🐦 @will_ins_Gruene

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,

He/him. Gay guy from London, very ex-physicist, into all kinds of science and geeky stuff. Left wing, when's the fully automated luxury communism arriving?

Animagus. Hearty but not hale. Celebrant of beautiful action. Likes bicycles. Note: The only time I post with my real name is in scientific journals. Kaurna Co

New main account: @violet.eurosky.social #PwME #MEcfs #PoTS #CPTSD #MCAS #SFN #FQtoxicity #CR41W #IchBinArmutsbetroffen Wishlists: https://paths.to/Viole

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

Livet har alltid og til alle tider handlet om å henge i ei liane utfor et stup, med en tiger over og en tiger under, se en mus komme og gnage på liana, strekke

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