Clay Crosby
psychotherapist, dad, erstwhile crooner
pwME caregiver and ally
CA Marriage and Family Therapist, Heilpraktiker für Psychotherapie,
EMDR Certified Therapist, AAMFT Approved Supervisor
#MECFS #MillionsMissing #NEISVoid #EMDR
@stardust949.bsky.social
Aspiring to write for stage & screen. Dyslexic ball of chaos. She/ her. #pwME #MECFS #POTS #BLM #TransRightsAreHumanRights. Twitter account: @StarDust949
@frozen.bsky.social
Dad, ally, and keeper of digital receipts | #MECFS since 2004 | #LongCovid since 2020 | Archivist by training | 🇨🇦 by choice | @frozen in the old 🐦 country | he/him
@immunofever.bsky.social
Immunoengineer at MIT BE developing predictive diagnostics. Captivated by #inflammation, #SexDifferences #Lyme, #COVID, #IACI, #IACC and #onehealth. Mom of 2. prev/ PhD in Immunology @Yale; PostDoc @Stanford https://talresearchgroup.mit.edu/
@berrybuzz.bsky.social
gardener | swiftie | tn1 | cats 🌈 clean air/water/soil/food 🌸🚪the garden gate
@yeslek.bsky.social
On hiatus due to Myalgic Encephalomyelitis Profile: smiling human, eyes closed and partially covered by hand, in black and white filter
@mariannehout.bsky.social
Dutch. Bedbound with severe ME. Trying to find my way back to life.
@turnoftheshrew.bsky.social
Here for the latest research + advocacy for Long Covid, ME/CFS, dysautonomia, connective tissue disorders, etc + disability justice community. Former HCP.
@mewarriorau.bsky.social
ME advocate longing for a cure, or some form of treatment. Mum of 3, grandmum of 3. Lived with the horrendous & disabling disease #ME (not CFS) for 28 years. #MyalgicEncephalomyelitis #pwME #MyalgicE (#MECFS #CFS) #LongCovid #ChronicIllness
@drsarastyles.bsky.social
Academic. #Nutrition + #Behaviouralscience 🥬 🍰 Has chronic fatigue syndrome (#mecfs #pwcfs) Upstate New Yorker living in #Ōtepoti, #Aotearoa. #Dunedin, #NewZealand. She/her.
@longcovidjustice.org
We are leading grassroots efforts to confront the Long COVID crisis, while centering racial, social, economic & disability justice. Our work is done by and for chronically ill & disabled people, our families and communities. linktr.ee/longcovidjustice
@phoenixme.bsky.social
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
@lguterman.bsky.social
Science journalist with long covid. Former staff at Science Magazine, Science News, C&EN, Chronicle of Higher Education. Now full-time patient.
@helen04.bsky.social
Severe end of moderate ME. Need to find my people again so I can feel validated and understood. Hoping they’ll be somewhere here 😌 #myalgicencephalomyelitis #MEcfs #pwME #fibromyalgia #fibro Also enjoy #crochet #CoD #BlackOps6 #F1 #Wales 🏴
@abrokenbattery.bsky.social
Severe ME patient currently on a 10% battery, the gas goes out more than I do. I also compile ME/CFS Awareness videos. https://linktr.ee/abrokenbattery
@danwyke.bsky.social
M.E. inactivist, person-centred counsellor, recovering poet (Rack & Waterloo Press)
@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
@jannamoen.bsky.social
Postdoctoral scientist studying the neurobiology of #longCOVID in the Iwasaki lab @ Yale. Patient, scientist, advocate. | ♿🏳️🌈 | she/her My long COVID research newsletter: lcbreakdown.substack.com
@diatoma.bsky.social
Ella/she/her. I write, I read, I draw plants. Chronically ill en la Ciudad de México. #ME #MECFS #POTS #LongCovid
@apeskygirl.bsky.social
Tree hugger with ME/CFS since 1992. #MEAction volunteer. Patient Advocate. OMF & Stanford Study Participant. ME/CFS • ND • POTS • EDS • One of the Millions Missing. Former Copywriter and Art Director. Now I watch squirrels and make things.
@vladvexler.bsky.social
Philosopher - ethics, politics, music | Slowly writing a book on Isaiah Berlin | Born in USSR, home is London | Living with ME since 2003. youtube.com/vladvexler (main channel) youtube.com/vladvexlerchat (chat channel) youtube.com/@vladvexlerphilosophy
@emilyesfraser.bsky.social
Former doc filmmaker/cinematographer/teacher, current full-time sick person, occasional poet
@lauraannecasey.bsky.social
@wsjmag / @wsj / @IAPE1096 board Journalist. Past: WSJ Trust fellow, disability coverage. Views are my own. NYC https://www.wsj.com/news/author/laura-casey
@mileswgriffis.bsky.social
Co-founder/editor @TheSickTimes.bsky.social Columnist @HighCountryNews.org miles@thesicktimes.org #LongCOVID
@alicefricker.bsky.social
20, Bedridden for 9yrs with #VerySevereME #hEDS #SFPN #MCAS #PoTS Chronic Insomnia & Chronic Bladder condition. Mother helps run account. ♥️ Instagram : @aliceandthemillions / alicefricker
@ruthlampard.bsky.social
Looking out for blessings: in wildlife, nature, & kindness. Lead Chaplain with AfME Healthcare: views my own. Living w ME & LongCovid. Virtual Pilgrim. Fan of rewilding, life too. Usually moderate to mild in views, occasionally sharp. No DMs, will block
@tilmanandris.bsky.social
Philosophy graduate | former science event organiser | former performance artist | ‘former’ and ‘ex’ at most of everything due to #MEcfs
@kristinwrites.bsky.social
Poet, Wife, Mom, LongCovid/MECFS Sufferer. Looking to connect and learning to advocate. Cofounder of #CripCoop. EIC, Poetry @epistemiclit.Bsky.social, @whirligiglit.bsky.social. Micropoetry chapbook Lift the Mask available widely. www.kristinhoulihan.com
@melindaiscomplex.bsky.social
My body has given up but I haven't... ME/CFS Patient Leader & Complex-Chronic Disease Advocate (on hiatus). Co-founder #MEAction Maryland. Bed-tethered disabled by severe ME & LC & comorbids. Orioles/Ravens/Caps fan. She/her
@bethmazur.bsky.social
#pwME and science/data nerd. co-founder #MEAction. Mostly post about #millionsmissing, #MEcfs, #LongCovid, #microbiome, #MCAS, #POTS, #citizenscience, and #healthequality. CS @MIT
@betsyladyzhets.bsky.social
editor/co-founder @thesicktimes.bsky.social | journalist covering Long COVID & related crises | she/her/🏳️🌈 email: betsy@thesicktimes.org | signal: betsyladyzhets.25 | https://thesicktimes.org/
@lisamccorkell.bsky.social
formerly a patient-led research collaborative co-lead, always a co-founder | MPP | she/her | natures 10 in 2022
@putrinolab.bsky.social
@auroraaus.bsky.social
Aurora Lady. Artist. Long Covid, ME/CFS. Reader. Vintage stuff. Tasmania.
@jimlebrecht.bsky.social
Co-director, Co-producer, with Nicole Newnham, of the documentary Crip Camp. Filmmaker, disability rights and justice advocate/activist, Co-founder of FWD-Doc.org. #Save504
@stickmancomms.bsky.social
Stickmen helping to build understanding and acceptance of hidden disabilities and chronic illness, in a way that empowers us. (Run by Hannah Ensor - who has #hypermobility #PoTS and probably other stuff.) +talking about personal experience of #disability
@jenniferlunden.bsky.social
Author of AMERICAN BREAKDOWN: Our Ailing Nation, My Body's Revolt, and the Nineteenth-Century Woman Who Brought Me Back to Life. She/her.
@katieklocksin.bsky.social
One of the #MillionsMissing with #LongCovid #MECFS // Once a radio and podcast producer, always a Transom alum 😷 Long covid is common 😷
@mildtin.bsky.social
Usually a lurker, Chronically Online for #LongCovid and other #IACC | Australia
@turnipcub.bsky.social
I would have you be a conscious citizen of this terrible and beautiful world.
@kjkrathwohl.bsky.social
Out of spoons lady of perpetual rest w Infection-Associated Chronic Illness 20+ yrs #MECFS, #FM, #Lyme & Co, #LongCovid 🌻 Advocate for bodily autonomy & Counting every vote 🌻 Art 🌻 Form. USPS, arts org 🌻 #MillionsMissing
@btreidler.bsky.social
PhD Cal Berkeley, Rocket Scientist, investment professional. Avid hiker, distance runner, and cyclist. All gone now due to ME/CFS worsening 2019.
@dualiejulie.bsky.social
(She/her) In LongCOVID/M.E. hell looking for a way out! First wave Longhauler. Former engineering student. Trying to get my personality back from the disease. Very cute dog.
@sassyauntiek.bsky.social
Science nerd, show me the data. she/her 🏳️🌈-ally, 🏳️⚧️-ally, BLM, pro-choice, ME/CFS, chronic illnesses & Endometriosis suck. what I say ≠ advice
@beton.bsky.social
Chronisch krank u.a. ME/CFS, SFN, MCAS Antifaschistin, Gartenliebe, Stadtfotografie (soweit möglich) Irgendwie in Wien gelandet
@privilegienschreck.bsky.social
me/cfs, shitposting, antifascist sie/ihr, they/them