Cort Johnson
Long (long) time person with ME/CFS/FM, Translator ME/CFS/ fibromyalgia/long COVID/POTS, etc. research and advocate. Creator of Health Rising and Phoenix Rising. Roaming the western US since 2012
@andrewgiffordphoto.bsky.social
Hello, welcome :) This Invisible Illness: my first long form photography project, about ME/CFS a complex & challenging health condition - like Long Covid. https://linktr.ee/andrewgifford.photography Bristol, UK. 335.42 ppm. He/him/oi.
@mecfsskeptic.bsky.social
Exploring the history of psychosomatic medicine and research on myalgic encefalomyelitis/chronic fatigue syndrome (ME/CFS). https://mecfsskeptic.com/
@lukelukeluke.bsky.social
I’m not here to post my THOUGHTS. I’m not here to share IDEAS. I’m here to post PICTURES OF MUSHROOMS and BE AN IDIOT Sign up for mushie-mail: cheerful letters filled with stickers, prints, and other goodies > Patreon.com/luke_venechuk
@geoffreymesbahi.bsky.social
PhD - Agroecology and animal husbandry. Grasslands, agroforestry, ruminant nutrition and animal behaviour. FiBL, Switzerland 🇨🇭 He/Him
@organicbotanic.bsky.social
Health academic, #IDSky, sailor⛵, photographer, botanist🌿, writer. Memoir, poetry, children’s stories. AI, public health, education, climate, UCU, films N Ireland 🇪🇺 Avoid🦠Covid. Photographs mine unless credited X: @organicbotanic Blue Sky 3/9/23
@rainsong.cloud
Artist, AuDHD, disabled, bi & non-binary. Homeschooling because covid. Pfp, white lightly fem-presenting face, short dark hair, glasses, blue lipstick. Banner is abstract kalaidescope swirls. Used to be Rune but Nazis suck and ruin everything.
@chronicallylinz.bsky.social
scientist, artist, stack of illnesses in a trenchcoat; listening, learning, trying to do better. disabled #pwME - no energy for anything much. she/they.
@kathdennis.bsky.social
Advocate Post-Acute Infection conditions, ME, LC, West Nile virus|prev @MSF|prev RN| disabled by a 🦟
@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
@mecvsvereniging.bsky.social
Patiëntenvereniging die zich inzet voor mensen met ME/cvs en hun omgeving. Op naar meer erkenning, kennis, steun en zorg voor ME/cvs patiënten. www.me-cvsvereniging.nl
@dxrevisionwatch.bsky.social
Formerly monitoring/reporting on developments with ICD-11, ICD-10-CM, DSM-5, SNOMED CT & other classification and terminology systems
@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
@millionsmissingfr.bsky.social
Asso de patient·e·s. Pour la prise en charge de l'encéphalomyélite myalgique #EM en France et le développement de la recherche. Entraide & soutien 🤝 www.millionsmissing.fr. #MECFS #EMSFC #pwME #paEM #MillionsMissing . Member of the World ME Alliance.
@therealmecfs.bsky.social
Chronically ill & disabled person with lots of personal opinions, who sometimes likes a hat. Occasionally an advocate for PwME, gamer and proudly on the Autism spectrum. I’ve low tolerance for ignorance and assholery so if you come for a fight, expect one.
@swastrosarah.bsky.social
Speaking up for everyone affected by severe/very severe #ME. Medical science has everything to learn about human biology from the post infection disease ME. #MEKills backstory https://x.com/swastrosarah?lang=en-GB
@daryllmarie.bsky.social
Bioacoustician & PhD student using sound to study baleen whale movement ecology 🐋 Wildlife photographer, birder, nature nerd 🪶 linktr.ee/daryllmariewildlife
@lolahachi.bsky.social
Love reading about wildlife, science and social justice. Chronically ill and disabled SevereME LongCovid ME/cfs
@grachstephanie.bsky.social
Physician specializing in ME/CFS, Long COVID, & associated complex disease | Assistant Professor of Medicine | She/Her/Hers | https://t.co/TkYm2MXvir
@cyruxime.bsky.social
Energetically compromised (bedridden) by severe #MECFS. All systems operating at minimum capacity & overloaded. In a previous life: comp sci x math, powerlifting. #LongCovid ally.
@dsavannah.bsky.social
~ Life stolen by MEcfs-hEDS-fibro-POTS-&c; FT sick since 12/2014 ~ #LiveInBedButIAintDead ~ When brain & body behave: Chronic Illness Advocate ~ Discworldian, Browncoat ~🐱(x3)🐢💐🌻🌷📸📚🖼️ ~ she / her ~ Love Is Love ❤️💚🧡💛🩵💙💜🤎🖤🩶🤍🩷 https://linktr.ee/thedsavannah
@simonmcg.bsky.social
Sometimes try to explain and comment on ME researchh, or even contribute to it. And I advocate for more and better research.
@talmandaniel.bsky.social
Curious & exhausted peace seeker, co-host of Post-Exertional Mayonnaise podcast, photographer and blogger. PwME, sidelined social worker, grief dealer, joy peddler, SAFC fan, He/Him
@longcovidlad.bsky.social
Long covid since April 2020. R 50 participant. Trying to navigate a plethora of health conditions without any NHS support. #ME/CFS #POTS, #Long Covid, BBB dysfunction, #SIBO, #Leaky Gut, reactivated infections, #MCAS, Clots
@jamellebouie.net
The real jbouie. Columnist for the New York Times Opinion section. Co-host of the Unclear and Present Danger podcast. b-boy-bouiebaisse on TikTok. jbouienyt on Twitch. National program director of the CHUM Group. Send me your mutual aid requests.
@bookhaven.bsky.social
Neurodivergent library ghost 👻 Napping instead of making lemonade 😴 ♿🦓🛏️ 😷 📚🚀 Don't share my posts on other platforms without asking. Header: Will Santino 🍋🥛 PFP: Pies Are Awesome 🥧
@jaleme.bsky.social
@compulsiveobserver.bsky.social
Installation artist. Perfume fanatic. Chronically ill. Concordia University PhD student(disability studies + performance studies + practice-based research.) Ex jammer, current failure. She/her Montréaler in Edmonton. https://linktr.ee/ChloeLum
@restthingever.bsky.social
formerly{{Passionate Software Developer. Guitarist, singer, songwriter. Foodie and traveller}}. Lover of Art Déco, geometry & Sci-Fi. Struggling with ME/CFS since 2020. Currently at Bell 40. Based in 🇨🇭 #MECFS #pwME #MyalgicEncephalomyelitis
@moerakijo.bsky.social
#LongCovid #WearAMask😷 books, libraries, histories, dogs she/her Aotearoa New Zealand
@rachelgraves.bsky.social
Haver of all the diseases. Mask wearer. Political obsessive, JD, (former-ish) newspaper reporter. Lover of Tacoma & the PNW. In a relationship. She/her.
@moleyme.bsky.social
Lancashire Lass with #MECFS likes flowers 🌸trees 🌳nature 🌱climate ⛈️ justice for all 👩🦽 interested in #longcovid prefer to interact a with community of kind humans ! . North West England . Feel like a Mole in an #MECFS hole trying to dig my way out!♿️
@mildtin.bsky.social
Usually a lurker, Chronically Online for #LongCovid and other #IACC | Australia
@louiseathome.bsky.social
Patiently (mostly) persevering with pacing #LongCovid #pwME #MECFS #POTS 🏳️🌈😷 cats • science • cats • FPL • cats
@safety.bsky.app
Sharing updates about trust and safety on Bluesky. This account’s mentions are not actively monitored. To report a post or account, use the in-app reporting feature. Community Guidelines: https://bsky.social/about/support/community-guidelines
@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
@janetdafoe.bsky.social
ME/CFS patient advocate and caregiver. Mom to Whitney. Spouse of Ron Davis. Child Psychologist.
@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!
@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 🇬🇧 & 🇳🇱
@sabrinapoirier.bsky.social
#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
@carriemcginn.bsky.social
Infection-associated chronic illness advocate | Life sidelined by #LongCovid #MECFS #POTS | #PatientPartner | MSc | Mom | She/Her | 🇨🇦 #Canada #Quebec #CovidConscious #StillMasking #MyalgicEncephalomyelitis #pwME #EMSFC #CovidLongue #CovidLong #pwLC
@erinbiba.bsky.social
Freelance Science Journalist. Fact Checker. NatGeo, BBC, SciAm, NBC News, PopSci, WIRED, and others. Hire me to fact check your book. I post about Jewish stuff, disability, Star Trek, and The Buffalo Bills. Jersey girl.
@joolie.bsky.social
I'm @jmatwood on Twitter. Featuring: Immature/informative/TMI posts about: birds, plants, bees, disability, chronic illness, silliness, my own health, etc 🦜🌱🐝♿😷🪿🏥 #pwME NO TERFS, NO UNSOLICITED ADVICE User pic is from Effin Birds (used w/permission)
@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/