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.

Ein freundliches Hallo an alle :) (she/her) "One day at a time. We cross the bridge when we get there" Bibesch Header: Ein Rüsseltier Bibesch Profilfoto: G

Living with Myalgic Encephalomyelitis and Postural Orthostatic Tachycardi Syndrome, so no longer working. Married, and have two grown up daughters.

💙UK Registered Charity: 1205685 💙Long COVID doesn’t stop the care - neither do we. 💙Join our Campaign: #SafeAir4All

Surviving MyalgicE aka ME/CFS & AAG to tell the story, pwME & advocate w/ a JD. Into MEdical, Social, Climate Justice & Arts. ME-dical apolide, Human Neutrino,

Living with Long Covid. Doing my bit to support UK healthcare workers with Long Covid. Chair of Supporting Healthcare Heroes UK. Associate Member Long Cov

Clarinettist. Conductor. Caregiver. 4 cats, 2 kids, 1 husband.

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

Housebound by MECFS, mostly bed/ Sofa since 2022 Bildschirm triggert PEM, deshalb selten hier & Energiebudget reicht nur für liken und weiter verbreiten Lebe in

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.