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.

🏴󠁧󠁢󠁳󠁣󠁴󠁿🏳️‍🌈Human She/Her. The original and best Minion Herder since October 2014. Not on Xitter. /a'na:l naθ'rax, u:rθ va:s be'θud, dox'je:l 'djenve:/

we will win. "I would very much like to be excluded from this narrative." civis civitatis novi eboraci. dum spiro spero.

Former healthcare worker #MECFS #FM

Senior Advisor, UC Berkeley Labor Center (retired). All views are my own.

ME researcher at the University of Edinburgh.

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

🧬 Biology of ageing 🌍 Exploring systems, synthetic, regenerative, computational biology, and complexity science 🇪🇺🏴󠁧󠁢󠁳󠁣󠁴󠁿😷

Writer, Musician, pwME.

20+ yr biotech atty at www.adkinscounsel.com, vaxxed and wearing a mask, and happily reacquainting myself with the 8-yr-old tree-climbing, horse-riding, fearles

Professor. Co-Chief-Editor Environmental & Resource Economics. Behavioural, Environmental, Experimental, Development. Mostly Ibaraki. バーコードなし. Sky Blue.

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,

Twin Peaks, Long Covid, tarot, bipolar, Buffy, wrestling, cats (sometimes wrestling cats). I correct people for money.

Queer. Autistic. Polyam. Bleeding edge of GenX. Childless, no cats. She/her ME/CFS, Fibro, POTS A former Hoosier now in Kentucky via Pennsylvania and Colora

Disease genomics & molecular mechanisms; ME/cfs: http://decodeme.org.uk, SequenceME @ Edinburgh University. Views - my own. He/him.

Plants. Cats. ME/CFS. Paleobotany, dinosaurs & earth sciences. Medieval History. #Disabled #FreePalestine #TransRights #Anarchist They/them Wales. #GardeningWit

ME-dically gaslit for 10yrs.

♿ australian living on unceded wadarni noongar land (southwest WA)・she/her・very sweary! #SevereME #POTS #auDHD #OCD #cPTSD #CSAsurvivor #AccessibilityMatters #D

Covid informed #PlusLife user looking for all the smart people I followed on the other place… #MECFS ally #sisterofpwme #millionsmissing #cleanair #covidisairbo

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.