Linguist
Senior Lecturer, La Trobe University
gesture/grammar/✨emoji/#lingcomm
Podcast: @lingthusiasm
Masto: superlinguo@scicomm.xyz
Blog: superlinguo.com
She/her(/they)
Discover the #ImmuneSystem with #StructuralBiology. We 💗 powerful #Tcells and #viruses. From one of my student “the GRAS is greener in our lab”. #scienceIsFun
Unofficial account exploring the intersection of biology, molecules, science, AI and protein folding with AlphaFold.
ME researcher at the University of Edinburgh.
Virologist focussing on all things influenza and SARS-CoV-2
Severe ME/CFS patient and advocate. Writer, photographer, filmmaker. artist, activist, creative. Bedridden since 2013 sick since 2004. Never. Giving. Up. ✊
ME/CFS patient advocate and caregiver. Mom to Whitney. Spouse of Ron Davis. Child Psychologist.
Senior Fellow in Public Health and Journalism, Center for Global Public Health at the University of California, Berkeley. I blog at Virology Blog (virology.ws). My academic position is largely funded by donations from patients. davetuller@berkeley.edu
Non nobis solum nati sumus. Husband. Dad x3. Upstreamist. Pracademic. Oregifornian. Storyteller. It’ll be ok in the end. If it’s not ok then it ain’t the end. Alphabet soup after my name: DPT PhD MPH OCS. https://www.linkedin.com/in/todd-davenport-2795ba10
PharmD, MS in Biophysics, PhD in Biochemistry
I like taking photos of weird things inside the brain 🔬
Cure #LongCovid
Long Covid Advisory Team: https://whn.global/long-covid-advisor.
daniellebeckman.com
Plant scientist studying how climate change affects plant toxicity (#cyanide). Born 314ppm.
Interested in science, tech, plants. #MECFS ally #botanist 🌾🪴🧪🌱🌿💉
Views my own
https://simondelfavero.com
PhD candidate researching ME/CFS at La Trobe University
📍Melbourne, Australia
Professor at the University of California Santa Barbara focusing on polycystic kidney disease, metabolic health and other things.
https://labs.mcdb.ucsb.edu/weimbs/thomas/
Long COVID/ME interested lung doctor | Campaigner | Independent SAGE | Co-Founder South Asian Heritage Month | Diversity Power List 24/25
Website: https://thelongcovidclinic.co.uk
Linktree: https://linktr.ee/binitakane
Ella/she/her. I write, I read, I draw plants. Chronically ill en la Ciudad de México. #ME #MECFS #POTS #LongCovid
Lily. #pwME, pwPOTS, Pokémon fan (she/her).
Researcher, FASSA. Employment relations; labour markets; economics; pol science; gender; climate & finance; science; birdies. Carmichael Fellow at Centre for Future Work, Australia Institute, but views mine. Meanjin (Brisbane) & Tāmaki Makaurau (Auckland).
Dad, ecologist & conservation scientist living on unceded Wurundjeri Country in Narrm. He/him.
Research: https://euanritchie.org/
The Conversation: bit.ly/2rjBg9A
Nature, SciComm, Politics, Music, Shodan🥋, 🏀, Carlton FC
🌈 Ally Born: 331 ppm CO2
#ME, #POTS, #LongCovid, former academic now 98% bedbound, progressive politics junkie, WoSo fan
I'm nobody. I like interesting people
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.
“I’m a natural blue “ Lifelong Dem. Will always default to fighting for the marginalized. Will follow dogs and people with dogs in their profile immediately. Shooting me a purposeless DM will get you blocked
Leftist | MS - Cybersecurity | Skateboarding | Bodybuilding | Video Games | Live-streaming | Writing | Painting
I have a million hobbies and tend to dive into things head first with reckless abandon.
Patient-Led Research for #LongCovid! http://patientledresearch.com
Research, algorithmic art & music, machine learning, anti-bias in AI data. #LongCovid research & advocacy @patientled.bsky.social.
95% of posts on #MyalgicEncephalomyelitis, #LongCovid or #chronicillness.
With ME/CFS 37 years, severe ME 31 years.
@IrishMECFSAssoc trustee 28 years
26 publications in peer-reviewed journals
Social media: https://me-pedia.org/wiki/Tom_Kindlon
Bed-bound activist with severe ME/CFS.
ME/CFS, chronic illness, #AusPol, #USPol, climate justice, social justice, crochet, cats, sci fi. Views expressed are my own.
If I had any spoons, I'd be dangerous.
Boonwurrung country, Australia
Severe M.E. patient, person-centred counsellor (currently not practicing), recovering poet (Rack & Waterloo Press)
Immunologist | Flow Cytometrist
Immunometabolism, Infectious Diseases, Immune dysfunction, Long Covid & ME/CFS
Senior Research Fellow
Liggins Institute | University of Auckland
DysImmune Research Aotearoa
www.dysimmune.nz
🇳🇿🥝🩸🧬🧪🔬👩🏼🔬
#CommunityEngagement Expert. Life sidelined by #MECFS #MCAS #POTS #Fibro #Gastroparesis +
#MECFS & #LongCovid #ResearchPartner & #Advocate • Chair of #MedicalEducation Group • #PwME #Disability
(Unceded) #Canada
https://linktr.ee/sabrinapoiriercanada
Victoria, Australia. Former professional wordsmith. 15+ years living with the hell of myalgic encephalomyelitis (ME/CFS). Prone to so-called left-wing views & bingeing good TV 🤓
Author of one(1) book. Journalist. Economist. #rstats #mecfs #ausecon. May be found walking his dog in Melbourne, Australia.
Scientific Director, #MEAction
Stanford Med
Université de Montréal
TIME100 Health
#ME, #EDS, #POTS, #LongCOVID
Views my own
Disease genomics & molecular mechanisms; ME/cfs: http://decodeme.org.uk, SequenceME @ Edinburgh University. Views - my own. He/him.
Paediatric Radiologist, Aotearoa New Zealand
Following more immunologists than radiologists
#MECFS #LongCOVID and a bit of #MacDev #iOSDev
he/him
https://ddp.nz | https://dysimmune.nz
official Bluesky account (check username👆)
Bugs, feature requests, feedback: support@bsky.app
