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.

Most of the time a homebound chronic ill person living with my hubby and bunny (Sammie🪽 RIP 07/sept/26) in Belgium

Science, gardening, reading old church books

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

New main account of @violetta.bsky.social #PwME #MEcfs #PoTS #CPTSD #MCAS #SFN #FQtoxicity #TalkCollapse #CR41W Wishlists: https://paths.to/VioletsWishl

NZ museums and heritage aficionado, shoe fancier, curator baiter, demure chocoholic, and all-round-caffeine fiend. Personal views; Not those of my employer.

Senior researcher in bioinformatics, proteomics and immunology. Enthusiastic about science, biodiversity, mountains, and women's rights.

Prematurely grey. Former Fukushima resident. Born on Bindal country, grew up on Jinibara/Gubbi Gubbi country, now living on Ngunnawal/Ngambri country. Fandom Ol

Former DJ/Event Manager | Administrator #MEcvs Infokanaal (Youtube) | Advocate for more biomedical research for post-infectious #MEcfs & #LongCovid | 🇧🇪 🇪🇺

Immunologist curious about viruses, cancer, evolution and all things human Likes all #systems thinking and still working out all the #omics 🤓 #immunosky #medsk

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.