@raffic.bsky.social
🇨🇦 troubadour. children's champion. ecology. Raffi Foundation for Child Honouring. beluga grads.
@jcontraire.bsky.social
Interests: Civility | Democracy | Long Covid | ME/CFS | MCAS | Autism | PDA | Alexithymia | Repost/Follow doesn't imply endorsement
@disaballiancebc.bsky.social
A cross-disability voice in BC. Promoting a more inclusive & equitable society for people with all disabilities through direct services, community partnerships, systemic advocacy, research & publications. Since 1977. https://disabilityalliancebc.org/
@altnps.bsky.social
The official "Resistance" team of U.S. National Park Service. Our website: www.ourparks.org
@readysteadystop.bsky.social
Los Angeles she/they * writer * marine mammal naturalist * maker of things * retired🧟♂️herder * disability & neurodivergence advocate * aka giraffe party 🖤: cats, music, 📸, geology, orcas, astronomy, creepy stuff, tacos, deftones, crosses, nine inch nails
@wordcakes.bsky.social
Writer/editor/thrifter/recovering Winnipegger. Can whistle the theme songs to MASH and TAXI like a goddamn pro.
@fotografie1976.bsky.social
@sebajones.bsky.social
Long covid/ME since 2020. Literary fiction. Em dash fan. Retired junglist. Guiri Madrileño. Socialista.
@julietmwirigi.bsky.social
HHMI Hanna Gray Fellow | PostDoc WashU | PhD UT Dallas | Neuroscience | Pain pathways | Single-cell EVERYTHING | Neurons | Cell culturing | Computational work | human dorsal root ganglia
@karamclean.bsky.social
Chronically ill and chronically online. TV lover. Co-host of Transatlantic Watch Party podcast. Current faves: #911onABC #TheRookie #HighPotential #TheLincolnLawyer. Continuity errors and extras being extra are my thing.
@levarburton.bsky.social
Kunta, Geordi, Reading Rainbow guy. Flies twice as high… #bydhttmwfi
@siobhansimper.bsky.social
Full time ill/Disabled person (ME/CFS and now Long COVID) writing about disability and craft. #MillonsMissing. #MECFS http://chronicallysiobhan.wordpress.com
@jesshoneybadger.bsky.social
Chaotic good writer and scientist with severe, bed bound MECFS. Writing wholesome stories, science stuff, and funny anecdotes from bed. Lover of memes. jesshoneybadger.substack.com
@sfdirewolf.bsky.social
Author, editor, activist, cat lover. Founder of the Disability Visibility Project. #DisabilityJustice feed I created: https://bsky.app/profile/did:plc:65kss3ewg5ida5mjyuk73v5r/feed/aaaba7ikg4sho More about me https://linktr.ee/disability_visibility
@owasow.bsky.social
Asst Prof, UC Berkeley, Political Science. Study protests, stats & race: 1/ Agenda Seeding http://j.mp/agenda-seeding 2/ Race as a Bundle of Sticks http://j.mp/bundle-of
@luckytran.com
Public Health, Climate Justice, and Science Communication. Bylines in the Guardian, Washington Post, and more. WHO Fides member. Grist 50 Fixer. Opinions my own and do not reflect those of my employer. http://linktr.ee/luckytran
@thesicktimes.bsky.social
A nonprofit news site chronicling the #LongCOVID crisis. Founded by journalists @BetsyLadyzhets.bsky.social & @MilesWGriffis.bsky.social Website: thesicktimes.org Newsletter: thesicktimes.org/newsletter Donate: the-sick-times.fundjournalism.org
@exceedhergrasp1.bsky.social
Scientific Director, #MEAction Stanford Med Université de Montréal TIME100 Health 2024 #ME, #EDS, #POTS, #LongCOVID Views my own exceedhergrasp1 on Twitter
@rebeccacokley.bsky.social
Politics. Legos. Prince. #YNWA Obama WH. Disabled. Not a werewolf. 🇮🇪
@bennessb.bsky.social
currently: sick / haunted in Western Mass, host of No End In Sight - a podcast about life with chronic illness, creator of #NEISVoid | previously: Stories We Don’t Tell in Toronto | she / her
@physiosforme.bsky.social
A group of physiotherapists with a special interest in Myalgic Encephalomyelitis (ME) with the aim to improve physiotherapy management for people with ME Find out more at physiosforme.com
@openmedf.bsky.social
OMF is fundraising to support open, collaborative research to find effective treatments and a cure for ME/CFS, Long COVID, and related diseases.
@benhmecfs.bsky.social
ME/CFS patient advocate, Open Medicine Foundation science correspondent. Bedbound. Former: exercise physiology, biochemist in training, athlete-Powerlifter, PT, Gym Manager. Jazz grad/Musician. F1/Boxing.
@janetdafoe.bsky.social
ME/CFS patient advocate and caregiver. Mom to Whitney. Spouse of Ron Davis. Child Psychologist.
@itswhitneywitch.bsky.social
Disability Justice Living with ME, EDS, POTS, MCAS, vascular compressions, spinal comorbidities & more Ambulatory wheelchair user Cozy gamer, lazy gardener, hopeful baker
@brianvastag.sciencemastodon.com.ap.brid.gy
Occasional science reporter at The Washington Post and elsewhere. Disabled by complex chronic post-viral illness. Living on #Kauai #Hawaii. Sometimes […] [bridged from https://sciencemastodon.com/@brianvastag on the fediverse by https://fed.brid.gy/ ]
@longcovidadvoc.com
A non-profit social enterprise dedicated to people with Long Covid + ME. Shifting the paradigm one step at a time... https://www.longcovidadvoc.com/ 🛍️ https://longcovidadvoc.shop/
@dysautonomia.bsky.social
We are the leading non-profit advocating for over 70M people around the world living with autonomic nervous system disorders. Research, Clinician Education, Patient Empowerment, Public Awareness & Advocacy is what we do. DysautonomiaInternational.org
@thetyee.ca
Independent BC-based journalism swimming against the current. Paywall-free since 2003. support.thetyee.ca
@thebeaverton.com
North America’s Trusted Source Of News Patreon: https://www.patreon.com/thebeaverton Merch: https://the-beaverton.myshopify.com/
@nlizaki.bsky.social
#MEActionNetwork health activist. Patient, project manager, translator & polyglot. ✊🏾 #Stoic #WoC @NLizaki & @SaveLizNevra on Twitter. #MyalgicEncephalomyelitis since 6. 28 now. #PMDD #hEDS #POTS #MCAS #LongCovid
@adarkenedroom.bsky.social
One of the #millionsmissing || Raising awareness of the most severe form of #MyalgicEncephalomyelitis
@ankijoy.bsky.social
ME/CFS Warrior not by choice but destiny (Profilbild: sick not tired in Schönschrift, große Fahne: moderate ME, darunter ein Haus, vor dem ein Rollstuhl steht, während drumherum alles weggebrochen ist)
@christinabaltais.bsky.social
Artist exploring the intersection between art & advocacy, sharing my experiences living with ME/CFS
@joeblow604.bsky.social
Living with Myalgic Encephalomyelitis since 2011. Artist, Advocate, Creative Former Electro-Mechanical Prototyper Inclusive #pwME #MECFS #MCAS #POTS #Fibro #LongCovid #Disability #chronicillness #art #artist #painting #oilpainting #digitalart #photography
@covidchronicles.bsky.social
Chronicling my journey through purgatory, graphically. Former athlete/composer/writer/woodworker. Saddled with debilitating COVID-induced metabolic dysfunction since Nov 2022. #LongCOVID #LC #MECFS #PEM #SickJokes
@wanderingkayli.bsky.social
@wandering on Instagram ✍🏻 Disabled with Long Covid 38+ months Long COVID Researcher @sfu-fhs.bsky.social Master’s Student @sfucmns.bsky.social writing on biopolitics & Long COVID https://beacons.ai/wanderingkayli
@richardvallee.bsky.social
I play language. Mostly irreverent. Debugger. AI. Global warming. Integrity. Health. Science. Chronically ill punk rocker. I think about the future a lot.
@rebeccaweger.bsky.social
https://linktr.ee/rebeccaweger Chronically in bed with a phone, book, journal, remote, crochet project and 2 cats. Disability doula as I'm able. Mutual aid and community care is life. Chronically ill. Disabled. Neurodivergent. 🏳️🌈👩🏻🦼😷
@godpod.bsky.social
Creator of the Universe. Daily free newsletter & animated podcast here: https://www.thegodpodcast.com
@georgetakei.bsky.social
I’ve boldly gone into the clear blue yonder. Follow for more recipes and tips.
@whywhy.bsky.social
Doctor in psychology, proud participant of #RemissionBiome first cohort, #EDSh #MCAS #ME/CFS. The pandemic is not over. #CleanAir #MaskUp
@meadvocacyproject.bsky.social
The ME Advocacy Project is a grassroots initiative founded by individuals living with post-infectious illnesses Myalgic Encephalomyelitis and/or Long COVID. Unceded Canada