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.

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

One of #MillionsMissing since 2002 #MEcfs Diagnose 2021 🐦 @will_ins_Gruene

Interested in research into ME/CFS/MECFS, FND and related conditions. https://medium.com/@cfs_research

Our world is not pre-given, it's enacted. Physics of biology & cognition; mind & socio-material practices; political ecology. All views, expressed or not, are

Living with ME/CFS since 1983. An advocate since my diagnosis in 1988.

Gegen Stigmatisierung & Ungerechtigkeit Für evidenzbasierte (Psycho-)Therapie & Katzen

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

🍋eugenics leads to fascism🍋LC/ME/MCAS/lupus/endo🍋still with her🍋OG khive🍋smash the motherfucking white supremacist patriarchy on the right AND the left🍋

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