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.

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

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.

Zorbian lifestyle with a twist - including amongst other things: sequencing, genomics and extreme project management.

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,

ME-dically gaslit for 10yrs.

Horizontal advocate for #pwME. 🇳🇱 in 🏴󠁧󠁢󠁳󠁣󠁴󠁿. Ally. Cis. PwME/LC. Volunteer with @meactionscotland.bsky.social. He/Him. #SaveSavannah #BIPOCLivesMatte

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

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

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.