Coming here from twitter and I have no idea where to start
04.12.2024 23:13 — 👍 12 🔁 1 💬 3 📌 1
Yup! Now I just have to find everyone!
21.11.2024 23:35 — 👍 1 🔁 1 💬 1 📌 0
Here for science, nature, philosophy, mycology, history, advocacy, Afroasiatic languages, linguistics in general.
Medically-retired analyst w/ MEcfs. Epicurean. Humanist. Existentialist. DMV-area forager. SCA, Atlantia. Harvard, GSE. Tinzouline ⵣ♡.
Politically Queer 🏳️🌈🏳️⚧️ Biomedical Engineer
ME/CFS 10+ years
🇳🇴(de/dem) 🇺🇸(they/them)
#AssociateProf #CompBio #Omics #WomenInScience #LGBTQ+Ally #Scottish #PrecisionMedicine #HealthCare #MDx #ME/CFS #RareDisease #Informatics #SciFiNerd #LongCovidAffected
sites.uab.edu/cgds/ she/her
We’re a community of Covid longhaulers who have been brought together by this illness. We share the stories of folks who have been through it, who are going through it, and how they’re surviving it. #LongCovid #CovidIsntOver #CovidIsAirborne #CovidSky
42 - Disabled polyam queer non-binary femme, geek living in Ottawa, Canada. ADHD, C-PTSD, Bipolar, Chronic Pain.
Loves board games & 3D Printing. Retired CanFURence Co-Chair
PFP is by jambiird.bsky.social
Ask to DM because my DMs are off.
Pediatrician, COVID cautious, passionate about ADHD and mental health. Mom of young adults & sugar gliders. she/her/hers
Fellow peds, check out PedSky: https://bsky.app/profile/did:plc:xitpfrpmistljpssx3i6csfd/feed/PedSky
drkristenstuppy.substack.com
Not alive anymore, not dead yet.
ME/CFS stage 3, Bell-Score: 20.
One of the #MillionsMissing
www.anjazeutschel.de
PsychNP, Midwife, knitter, sci-fi and fantasy fan. Living with EDS and long covid. Still masking.
She/her, NHS GP in Scotland, #LongCovid sufferer, views my own. 😷💉💨🇪🇺
Disabled software engineer cosplaying as the classiest Avenger. Nerd, nature lover, neurodivergent, cat mom. ME/CFS 30+ years (No affiliation with Marvel) #MillionsMissing
Mostly bedbound by severe #ME/CFS #POTS #EDS #MCAS + more. Chronically hopeful for better days. Determined to fight against injustice so people with ME + Long Covid are treated with the same belief, respect + kindness as any other serious physical illness
Not-for-Profit Organisation supporting Australians living with ME/CFS (mylagic encephalomyelitis / chronic fatigue syndrome) and long COVID.
Education | Research | Advocacy | Support Services
Website: www.emerge.org.au
Donate: www.emerge.org.au/donate/
Covid killjoy, pro Palestine, immunocompromised, queer, gender hedonist
Living in the Netherlands. M.E. since 2019. Here to connect with the ME folks and researchers. english, dutch and turkish
Queer crippled writer.
Disability advocate
Tired
Occupational Therapy Lecturer at Australian Catholic University. Returned from UK to Brisbane. Interested in #MECFS #PWME #mentalhealth,#OTeducation
UChicago AB '17 in Mathematics. Don't ask me anything about math. 🙃 Severe #MECFS, always the party.
Blog: https://www.helfcare.com/
#Mother #Artist #Writer
#MentalHealth #PeerAdvocate Former #USNavy & #USMCFamilyReadiness #PWD #ChronicPain #PsA #MECFS #CRPS
#Survivor of #NarcAbuse #TTI #ProgramKid - that's me.🧸
; 💙💜Alive Day=10/25
#GenX #BLM #RESIST
🏳️🌈🏳️⚧️ #Ally
📍 #SanDiego
🚫🍊🤡🐔🌮
#Medsky,#UniversalHealthcare, #Single-Payer, #HealthEquity. #M4A, #Medicare4AlI, #HealthcareIsAHumanRight,
#Healthcare4All, #HealthcareForAll,
#DemandUniversalHealthcare,
also on FB & Instagram. DUH! No DMs
M.E. since 1976. In the golden rolling hills of California.
Looking at screens sets my eyeballs on fire so there will be pauses.
