Singing is the best medicine for whatever ails you. Covid Cautious out of love & humanity (& because I have Long Covid). A better world is possible. She/her.

NZ museums and heritage aficionado, shoe fancier, curator baiter, demure chocoholic, and all-round-caffeine fiend. Personal views; Not those of my employer.

HS teacher with AuDHD and a fondness for structuralism; disability advocate, student advocate, LGBTQIA+ ally. Worrying about the climate since 1978; fighting th

https://simondelfavero.com

#CannabisMedizin🥦 #MEcfs🪫😷 #IchBinArmutsbetroffen💣 #GGUltra📎 ᓚᘏᗢᗢᘏᓗ ✨Anne Brorhilker Fan Club✨ I may be sick, but I won't be still.📢 Profilbild, schlafend

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,

Chaotic mix of politics and ME/CFS

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.

he/him @sobyv@mastodon.online Inuk/Inuit Canada Disabled long covid +adhd

I play language. Mostly irreverent. Debugger. AI. Global warming. Integrity. Health. Science. Chronically ill punk rocker. We must know. We will know.

person with ME/CFS professional slug

ME after covid infection Feb'22. Bedbound. 🛌 #ThereForME #GreatestMEdicalScandal #PEM 🇬🇧🇲🇫🇪🇦🇧🇪

Retired My wife and I are a retired couple who live near Santa Fe, New Mexico USA.

Well, it seems I'm still on this plane of existence! Disability rights stuff, fashion history. Cumbria (UK). Autistic. She, for the moment.

Formerly assistant professor of philosophy • bedbound since 2022 with severe myalgic encephalomyelitis, a type of long COVID • philosophy of science, epistemolo

Severe ME/CFS, mostly bedbound. @voxem.bsky.social

Life on hold by severe #MECFS, currently 99% bedbound 🛌 Documenting my life like it is now, advocacy through photography 📷 📍Finland https://nikosuvisto.c

God first! | #mecfs | Oecotrophologin | Redakteurin

Disabled by very Severe Post-COVID ME/CFS. Not always able to use phone. Bedridden. Unable to Speak. I care. Ⓐ💚, (FR/DE/EN, but posts in english) Clinging

Sou'West UK. Have M.E. Likes; Nature, engineering, brewing and history.

New main account of @violetta.bsky.social #PwME #MEcfs #PoTS #CPTSD #MCAS #SFN #FQtoxicity #TalkCollapse #CR41W Wishlists: https://paths.to/VioletsWishl

Die Büroklammer war nervig, aber sie wollte nur helfen. https://youtu.be/2_Dtmpe9qaQ?si=B73eFFE0YzSoQ94t

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

Es gibt immer noch eine große Lücke zwischen dem, was die Öffentlichkeit über COVID-19 weiß, und dem, was sie wissen sollte. Deshalb hier Infos über COVID-19.