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.

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

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

#ME/CFS Betroffene und Aktivistin (Liegenddemo Köln) echt #kölsch Mädche https://youtube.com/@initiativeliegenddemokoln?si=iIVmVB-FGFyTExsO Studien zu COVID-1

Hauptsächlich wegen aktueller Covid-Information hier (leider nicht beim ÖRR verfügbar) - nur selten da Es ist cool Ingenieurin zu sein (wenn man uns die Welt

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

Grief support & writing workshops to help you heal ancestral relationships, connect with nature, and to put your best story forward. #AuDHD #spoonie 🏳️‍🌈🏳️‍

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.