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.

Trying to live a greener life. Grateful to everyone who takes the time to share their experiences and knowledge. Wear headband Laianzhi KN95's and 3M Auras. No

Poverty-Brexit-Trump+Climate=BigMoney Mess. Fan of Logic, 360° Info, open-mindedness, innovative science, thinking out of the box+truth. Question everything Wok

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

Evidence-based medicine over eminence-based medicine. #MECFS

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

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

This account will prob be about biomed research—complex chronic illnesses and Covid—w/some material on disability justice and organizing. ME ‘05, LC ‘23, many

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