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

Owned by a cat. Refugee from the hell place. ME/CFS for 34 years and counting. "Anti-recovery activist" ( some chance!) Boring.

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

Severe ME patient currently on a 10% battery, the gas goes out more than I do. I also compile ME/CFS Awareness videos. https://linktr.ee/abrokenbattery

Vegetation ecologist & research laboratory manager - on pause (MECFS / LC). Also: fire behaviour, libraries, cultural preservation, music, guinea pigs, TNR cats

Housebound by ME (myalgic encephalomyelitis), married, has a dog, agender, AuDHD, lives in the forest. Gender neutral pronouns preferred. Trying to be kind.

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.

#DieMaskebleibtauf, #NoAfD, #NoFacism, #NoRacism

I play language. Mostly irreverent. Debugger. AI. Global warming. Integrity. Health. Science. Chronically ill punk rocker. I think about the future a lot.

ME. Spouse w LC, ME. Writer, bread baker, daydreamer. Still waiting on fair funding and apology from HHS. Masking like someone’s life depends on it.

Lisa Smith. Writer, narrator, migraine advocate, connector of dots, Masshole. Sarcasm free of charge. She/her. (I block lots of ppl for tons of reasons, rarely

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.