@putrinolab.bsky.social
@thetweedy.bsky.social
Corin • PhD at UBC Geography • dissertating on cats • literal mutant (EDS, etc.) • AuDHD • crip/queer/trans • he/him • the_tweedy on Twitter but rarely active over there
@amyboylanwrites.bsky.social
Freelance #copywriter. PhD Geology. Life on ⏸ 1st 🌊 #LongCovid #PoTS #MCAS #LongCovidKids #CovidIsAirborne 😷
@amandalhu.bsky.social
Neighbour and pal to children, adults and nature. Pro-treating each other like we live in a society. I communicate about stuff for work and for fun (here, where my opinions are my own). She/her. 📍Mohkinstsis, Treaty 7 (Calgary, Canada)
@untonuggan.bsky.social
angry mast cells (HaT and #MCAS) + #POTS + neurodivergent. ♿ queer. white. emperor of typos. brain fog zone ⚠️. they/them 🎶 iii'm still masking 🎶 working on porting more of my body science infodumps and such to: liminalnest.wordpress.com #NEISvoid
@isabelrb.bsky.social
CEO | Renegade Research | Project Director of Remission Biome NBC-HWC, AIP-C @remissionbiome.bsky.social
@amblingshambler.bsky.social
She/her. 80's baby. Creative, ND, spoonie. Always dancing. Always singing. Very tired. I love to learn but my brain is mush, apart from random trivia, my hyperfixations and song lyrics. Great at DIY. Kindness is everything.
@andrewg76201347.bsky.social
ME/CFS, POTS, MCAS, lupus, Hashimoto’s. Patient & carer. Disabled scientist. Female - using fake name bc I post about son's illness. Location: Australia
@himmatb.bsky.social
Writer + editor on pause due to Long Covid/vaccine. Very severe and fully bedbound. ME/CFS | POTS | hEDS. he/him
@diatoma.bsky.social
Ella/she/her. I write, I read, I draw plants. Chronically ill en la Ciudad de México. #ME #MECFS #POTS
@nelehelena.bsky.social
I'll "tweet" here about the things I don't like if the other app goes down
@cabruce.bsky.social
Previously a psychotherapist. Bedridden #ME 32years Daughter severe ME, eldest son MS. I like art, nature, books, people, music, poetry and podcasts!
@uselesspriest.bsky.social
Long COVID, mild, since Apr 2022 ME / Long COVID diagnosed May 2024
@guusontheinternet.bsky.social
Creative turned activist #NietHersteld - Long Covid since jan’21 ♿️ - posts with brain fog, so pls bear with me - eager to learn - posts in 🇬🇧 & 🇳🇱
@wilhelminaj.bsky.social
Living with ME/CFS since 1983. An advocate since my diagnosis in 1988.
@angryhacademic.bsky.social
#LongCovid Scientific Consultant PhD Nutrition & Metabolism Hon Research Fellow, Lund Uni Posts: nutrition ▪ health ▪ all-things-science ▪ activism ▪ fun facts ▪ #PostVac Donations: https://ko-fi.com/drsmash Facebook: https://www.facebook.com/LongCovidSC
@katha1970.bsky.social
Here for research and info on #Migraines #MECFS #LongCovid #MCAS #MCS #ChronicPain #MetabolicHealth #Neuroscience #Psychology #MedicalGaslighting, posts German & English, hobby songwriter
@pamelarbishop.bsky.social
Was research professor, now disabled by #LongCOVID (12/7/20) & subsequent #POTS #MECFS #MCAS #SFN #cSVD Patient advocate when able. Tell your story if you can.
@68thmonkey.bsky.social
Previously an alien, but really a monkey. MECFS since 2017. ♿️🌈 Science, nature, climate, dogs, politics makes me mad but I just cant help myself. Peace & Love 😍✌️ (definitely not fear). Lucky to live in Bundjalung Country 🇦🇺 (Advocate for Bleats not Skeets)
@stevefifield.bsky.social
Informed decisions & verifiable facts please, not opinion & belief. UK. 🇬🇧 Mine of occasionally useful information. NHS and healthcare 💙 #Equality #Justbe #Inclusion #LGBTQ+ 🌈 ally #pwME #MECFS #Activetravel 🚲 #Sustainability #Gardening #VisibleApp
@lessorfewer.bsky.social
PhD geography: money & finance • Life mostly on hold from Long Covid 03/2021 • 개리말고 가리 ________________ 🇮🇪 | https://linktr.ee/g_a_r_y
@paulaknight.bsky.social
Author, illustrator, comics memoir THE FACTS OF LIFE (Myriad) Kidlit Books x3 Writing illustration comics poetry photography Disabled nonambulatory bedbased 6yr #pwME No DMs pls https://linktr.ee/paulajknight https://ko-fi.com/bedscape She/Her
@naomidharvey.bsky.social
Zoologist & veterinary research. She/her. 22yrs with #MEcfs Pro-vax but vaccine injured. Life on pause due to moderate/severe ME/CFS ♿️ Patient Expert in ME/CFS, POTS and syndromic Long Covid. Please excuse my typos.