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Ralf Wittenbrink
@ralfwittenbrink.bsky.social
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.
pinkelinse.bsky.social
@pinkelinse.bsky.social
Steve Fifield
@stevefifield.bsky.social
Informed decisions & verifiable facts please, not opinion & belief. UK. 🇬🇧 Mine of occasionally useful information. NHS and healthcare 💙 #Equality #Justbe #I
Ghost [inactive acct, moved to @B1t3b4ck ]
@b1t3f0rc3.bsky.social
MDNI ART FIEND >:3 '96 ϴΔ coyote werewolf gnc dyke thing™ 🏳️‍⚧️ ♿️ plural Icon by @kr00bs.com ♡ 📍western PA
Wilhelmina Jenkins
@wilhelminaj.bsky.social
Living with ME/CFS since 1983. An advocate since my diagnosis in 1988.
Elegant Sledgehammer FREE LINK
@tinyteerex.bsky.social
AuADHD. white. ACAB. Land Back incl Palestine. Mutual aid & solidarity. PFP: orange cartoon cat in bed w/ dark orange stripes & knife tail. Text reads: low on
Tom Kindlon
@tomkindlon.bsky.social
95% of posts on #MyalgicEncephalomyelitis, #LongCovid or #chronicillness. With ME/CFS 37 years, severe ME 32 years. @IrishMECFSAssoc trustee 29 years 26 publ
Richelle Sepulveda
@richellesepulveda.bsky.social
Long Covid, MECFS, ADHD, etc. Patient-led research is my jam. A bit obsessed with GIP.
thee agnes de buffle
@vanadiumzest.bsky.social
🍋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 ME/CFS Association
@irishmecfsassoc.bsky.social
Irish Myalgic Encephalomyelitis/Chronic Fatigue Syndrome Association-for Information, Support & Research NB: Posts ≠ advice. Registered Charity RCN 20100254.