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.

Bodybuilder😁, trans, Herbstfreak mit Yetigenen, Kuchenmöger und Schlafenthusiast. Spoonie und Chronic Badass. He/Him🏳️‍⚧️🦣

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

Retired FE lecturer, interested in nature and science.

She/her Halifax, Nova Scotia Halisky Long Covid Knitting Dogs & cats Urban gardening (zone 6b) Climate change Transit

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

Informed decisions & verifiable facts please, not opinion & belief. UK. 🇬🇧 Mine of occasionally useful information. NHS and healthcare 💙 #Equality #Justbe #I

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

Wannabe Artist. Making photos. Introverted, HSP. Still a bit sherlocked, right now a bit TWD-ed as well. Born in Poland, living in Germany. Team CovidIsNotOver/

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,

BUY CANADIAN #Pots #Dysautonomia #MCAS #ElbowsUp #Happy Doggo #Enhypen7 #SKZ #Ateez #BTS #&TEAM #Cortis #TxT #P1Harmony 🇺🇦 🏳️‍⚧️ 🏳️‍🌈 🇬🇱 🇩🇰 🇨🇦

Science defender and eco-worrier. (she/her) No DMs please (can't access).

Seit 2021 setzt sich die Initiative #ProtectTheKids für #saubereLuft in öffentlichen Innenräumen ein | #PublicHealth in Schulen und Kitas | #CleanAir4Kids | #Ai

Serendipidist in training

TwiXXer: @BavastroEva Mastodon:EvaBavastro@sueden.social Email: bavastro-eva@gmx.de Coronaschutzimpfung Stuttgart für alle ab 6 Monaten

Housebound by MECFS, mostly bed/ Sofa since 2022 Bildschirm triggert PEM, deshalb selten hier & Energiebudget reicht nur für liken und weiter verbreiten Lebe in

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.