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.

🏴󠁧󠁢󠁳󠁣󠁴󠁿🏳️‍🌈Human She/Her. The original and best Minion Herder since October 2014. Not on Xitter. /a'na:l naθ'rax, u:rθ va:s be'θud, dox'je:l 'djenve:/

Mainly plants

we will win. "I would very much like to be excluded from this narrative." civis civitatis novi eboraci. dum spiro spero.

They/E/She Disabled Genderqueer Bisexual Disaster, est. 1989 BLM ACAB 🍉 RPs may be 🔞 FFXIV NA: Naia🌊 Guldstyr🌟 Blooming🌹 pic: tacticiankate

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

Disabled by very Severe Post-COVID ME/CFS. Not always able to use phone. Bedridden. Unable to Speak. I care. Ⓐ💚, (FR/DE/EN, but posts in english) Clinging

Informed decisions & verifiable facts please, not opinion & belief. UK. 🇬🇧 Mine of occasionally useful information. NHS and healthcare 💙 #Equality #Justbe #I

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

I make good soup. Trans rights are human rights Black Lives Matter Women are equal Children have agency Artist/Burner/Disabled AuDHD/PASC/POTS/MCAS I ma

M.E(Over26years so far🐦‍🔥🪫🙄)🥄Depression,Millennial,Vegan🌱Sloth🦥Magpie✨Love:Animals🐾🐘,Piercings,Tattoos,Soaps,📸,Crystals💎LipBalm💄J2🖤1R🎵TT🎵+Coffee☕

I occasionally try to explain and comment on ME research, or even contribute to it. And I advocate for more and better research.

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

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,

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

Finance & Art. History & Sociology & Fashion History. ME/CFS & LC 🫩

ME/CFS patient advocate and caregiver. Mom to Whitney. Spouse of Ron Davis. Child Psychologist.

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

Socialism with Mr. Rogers characteristics Humanities and science oriented Harm Reduction Anti-AI Industry, Pro-Cybernetics Lover of orcs and beefy/big men A goo

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

Plants. Cats. ME/CFS. Paleobotany, dinosaurs & earth sciences. Medieval History. #Disabled #FreePalestine #TransRights #Anarchist They/them Wales. #GardeningWit

Was: Facilitation & organisational culture nerd for do-gooders; climate & sustainability. Healthy, athletic; MTB, ski, mountaineering, outdoors. Everything on p

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

Economist, writer, strange nerd. she/her. trans. lesbian. White, anti-whiteness. Opinions solely my own. On unceded Eno territory.

New main account: @violet.eurosky.social #PwME #MEcfs #PoTS #CPTSD #MCAS #SFN #FQtoxicity #CR41W #IchBinArmutsbetroffen Wishlists: https://paths.to/Viole

#EncefalomielitisMialgica #ME #MEcfs #EMsfc #CIE10-G93.3 #MillonesAusentes #CIE11-8E49

Interests: ME/CFS, Long Covid, politics, science, nature and animals. Norwegian but post mostly in English. Newbie allotment gardener.

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

23 | #MECFS #SFN | hausgebunden

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

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

Previously a psychotherapist. Bedridden #ME 32years Daughter severe ME, eldest son MS. I like art, nature, books, people, music, poetry and podcasts!

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

Author of "stranger and stranger”, letter writer, advocate and fundraiser for biomedical ME/CFS research.

Has the world gone insane? Brit in France. Ex-scientist. DPhil. Owned by cats. ME /CFS. Avatar: Proud Goose, Tui Sankamol

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