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.

🏳️‍🌈 ME/CFS | ADHS liegen aushalten durchhalten Film & Kunst Albtraum: Perimenopause! PB: Minimalistisches Kunstwerk von Monika Gardyla: 2 Halbkreise in N

Classical music and opera journalist. Blogs at irontongue.blogspot.com. Alto, martial artist. Former tech writer. Music, books, politics, food, public health.

#BEready, #Bern #Preparedness Offizieller Kanal. News rund um die BEready Kohorte. Motto: Bern, get ready. Impressum: http://www.BEready.unibe.ch

ME/CFS | Long COVID | IACC

Artist | Author of THE LANGUAGE OF TREES | Host of Sunday Salons | Rights of Nature 🌍 Long COVID 😷 Dysautonomia | Irish in NYC / Ardee | Born @331ppm | Clim

Myalgic Encephalomyelitis - M.E + POTS for 38 years Donor to the UK MEcfs Biobank for 10 years & @DecodeMEstudy Please watch http://dialogues-mecfs.co.uk/vide

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

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.

Anthropologist in the margin

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

ME. Spouse w LC, ME. Writer, bread baker, daydreamer. Still waiting on fair funding and apology from HHS. Masking like someone’s life depends on it.

begrudgingly online for chronic illness research & disability justice community. living meaningfully & unapologetically as a hermit against my will.

Interested in history, disability, politics, chronic illness. Loves animals, dry white wine, chocolate and my bed. Irish. ADHD, ME sufferer. Cat and dog pers

Disease genomics & molecular mechanisms; ME/cfs: http://decodeme.org.uk, SequenceME @ Edinburgh University. Views - my own. He/him.

Former fine violinist, disabled, medical editor, queerdo, feminist, Francophile, Californian, buddhist. DM = block. 🏳️‍🌈🏳️‍⚧️♿️ 😷; #medsky; Covid is airborn

Nebula-winning and Hugo/Sturgeon-nominated writer. Bagel the Dog's emotional support human. Dadjoke teller. Unrepentant punster. Sentence-fragment lover. Disabl

ME/Long Covid - existing mainly in the horizontal world. gaylemadeira.com

Katter, makt, odling, läsning, trams och oanständigheter. Skriver dåliga dikter om funkisliv och växter. Hatar oombedda råd. https://detsvartahalet.wordpress.c

Former professional ballet dancer | Bed/sofa-bound M.E. patient | Using BlueSky to raise awareness for #MyalgicE | #IACC I #PAIS #art2cureME #pwme #millionsmi

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

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

Lawyer. ME since Oct 2000. Mostly housebound since 2014. #ME #hEDS #dysautonomia #Citrate synthase deficiency #impaired oxygen extraction #celiac #mitochondr

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

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

Otherwise known as @KoparaFallsKid.bsky.social Movement As Medicine advocate. Follow my writing on Limberation.com Rheumatoid Arthritis patient. Previously di

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