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.

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

Lazy artist, with a love for snowboarding and mountain biking. Utterly horrified by our current human world. In order to change the world we have to change huma

Mom trying to make sense of it all....Long Covid, ME/CFS, CCI, EDS, MCAS, POTS.

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

(she/her), 40-something, (aro/acespec) queer, cat mama, nature enthusiast, retired nurse, spoonie, and advocate If you want to know something else, kindly ask

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.

Neurodivergent & disabled archaeologist, educator, writer & parent. she/they

Land back ✨️ Adopted/reconnecting RR Métis (Villebrun, Ducharme, Flammand, Bousquet, etc) Disabled 😷 and practicing #Doikayt on Skwxwú7mesh territory ♾️🇵🇸🧡�

Chaotic mix of politics and ME/CFS

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

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.