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.

German, English, Spanish Sociology, Medicine, General Practice

Mostly bedbound by severe #ME/CFS #POTS #EDS #MCAS + more. Chronically hopeful for better days. Determined to fight against injustice so people with ME + Long C

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

ME/CFS | Long COVID | IACC

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

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

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

Public Health, former MSF, Journo in past life, on a Zero Carbon mission. London, Hong Kong, Kunming, Chicago. 新聞自由 #EndFossilFuels #COVIDisAirborne

Retired UK journo and charity PR/fundraiser. Proud dad and grandad. Such an Oddfellow. Soft spots for @MillMedia.bsky.social, @newjournal.bsky.social and @Fenla

University of Sussex Social Policy Alumna; Carer; LGBTQ+/Disability ally; Hater of Fascists; Nature, Health, Science & Politics; Based in UK

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.