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.

LongCovid Leftism (the normal, boring kind)

ME after covid infection Feb'22. Bedbound. 🛌 #ThereForME #GreatestMEdicalScandal #PEM 🇬🇧🇲🇫🇪🇦🇧🇪

Medical doctor, Public Health, social medicine and medical informatics. Sozidoc on Wordpress.

Independent historical researcher (involuntarily self-taught), writing at a frustratingly slow 🐌 pace due to severe chronic illness.

ME-dically gaslit for 10yrs.

News and information about interventional trials for Long Covid, ME/CFS, POTS, and other post-viral illnesses. Message or tag me if you’re in a trial or otherwi

Ohne Gier wäre die Welt besser!

Collectif qui porte la voix des malades d'encéphalomyélite myalgique #EMSFC en France via des actions publiques et en ligne. To make #MECFS voices heard, voxEM

Crafter by necessity to stay occupied whilst dealing with health issues. MCAS PoTS Hypothyroidism (need T3 for life) ME. Please entertain me and let’s connect.

95% of posts on #MyalgicEncephalomyelitis, #LongCovid or #chronicillness. With ME/CFS 37 years, severe ME 32 years. @IrishMECFSAssoc trustee 29 years 26 publ

I studied computer science so I guess I must be a computer scientist. Or just some feminist bi poly geek. Cis. White. On the spectrum. Raumzeitlaborantin. Gesic

#MECFS lange mild | arbeitsunfähig seit SARS-CoV-2 2022 | #LongCovid #MCAS #POTS | Wissenschaft, Forschung, Therapie & Aufklärung | #MEAwareness 💙 | Hoffnung

Irish Myalgic Encephalomyelitis/Chronic Fatigue Syndrome Association-for Information, Support & Research NB: Posts ≠ advice. Registered Charity RCN 20100254.