@TheChronicCollaboration
@TheChronicColab
A resistance movement for chronically ill & disabled people. Joining the dots between conditions. Resisting psychologisation. Fighting for justice & equality.
ID:1429102862743875587
https://thechroniccollaboration.com/ 21-08-2021 15:27:36
4,9K Tweets
4,2K Followers
1,9K Following
Dan Wyke 🦠➡️🧠🔥
@Dan_Wyke
Patient advocate (ME/CFS), person-centred counsellor (see link), recovering poetME/CFS News
@MECFSNews
News, interesting information and commentary on ME/CFS. My bluesky account is @mecfsnews.bsky.socialtomkindlon.bsky.social
@TomKindlon
With ME 34 yrs, housebound 29 yrs. 95% of posts on #MEcfs/#LongCovid/#chronicillness. 26 publications in peer-reviewed journals. @IrishMECFSAssoc trustee 26 yrsKaty B
@KatyBruce108
Myalgic Encephalomyelitis - M.E + POTS 38 years Donor to the @mecfsbiobank & @DecodeMEstudy Please watch https://t.co/rPfzhZQ6po #pwMEdavidtuller
@davidtuller1
Senior Fellow in Public Health and Journalism, Center for Global Public Health, UC Berkeley. My academic position is largely funded by donations from patients.Wading through treacle
@kimisgubbed
Advocate & sharer of bio research for INFECTION ASSOCIATED CHRONIC DISEASES inc MECFS, Long COVID, MCAS, Dysautonomia, Vaccine injuries, FMS, Sjogrens & Lyme 🔬Carole Bruce
@CaroleBruce17
Chained to one room by severe #ME for 30+ years.Formally a psychotherapist. Mother of a daughter with severe ME for 38 years. Eldest son MS. ❤️Art, politics.Lizzy H
@hopefullizzy
28y/o creative, with complex health issues🤞🏼ME/CFS biomedical research. Passion for the wild, for kindness, and helping all people have a voice. Co-author✨It'sME(Jaime)
@exceedhergrasp1
Director of Sci & Med Outreach, #MEAction Stanford Med #ME, #EDS, #POTS, #LongCOVID Views my own [email protected]Jo
@cfs_jo
CFS(!) & POTS diagnosis, ME symptoms - trying to accept. Still me. Sense of humour intact. Also on Insta as JustJoHere and BlueSky as JustJoDr Asad Khan FRCP FRACP 🇵🇸🇳🇿🇮🇳🇬🇧#pwLC
@doctorasadkhan
Lung Dr on pause since Nov 20 #LongCovid #POTS #MCAS #HSD #pwME #Aotearoa Views my own; Retweets≠endorsements #freepalestine #TeamClots PLEASE READ PINNED TWEETBea is Chronically Persisting✨
@Be_Kinderr
Chronic Illness Researcher. Science of #MECFS #LongCovid #POTS #EDS #MCAS CCI SFN Lyme etc & How They Connect🕵🏻♀️Scientist/Advocate [email protected]Crafty Miss
@CraftyMissB
I'm Beth, embroidery & craft are my buzz. #socialist #pwme #disabled insta: thecraftymissb https://t.co/H4UqOa9igdPaula Knight
@Paula_JKnight
Author illustrator memoir THE FACTS OF LIFE (2017) Kidlit pic books x3. Reading audiobooks. Thinking about writing. Disabled. Bedbound 5yr+ v #severeME she/herDaniel Moore
@Talmandaniel
Curious & exhausted peace seeker, co-host of @pempodcast23, photographer and blogger. PwME, sidelined social worker, grief dealer, joy peddler, SAFC fan, He/HimPhoebe
@PhoebsBo
Life was once Leith, homelessness & a forklift truck. Life is now being chronically ill with ME & writing about it. Autistic. Smorky’s human. She/her.Alisontomyradio
@arisonsned
ME MCAS Lyme.Still with humour.Satire Music.Dream of life without illness. Wanna ride my bike. Cat & Dog Botherer.YP Counsellor retired. Retweet not endorsementDakota
@Dakota_150
ME/CFS, Long COVID, Dysautonomia & POTS AdvocateVlad Vexler
@VladVexler
Philosopher - ethics, politics, music | Slowly writing a book on Isaiah Berlin | Born in Russia, home is London | Living with ME since 2003. | 🔗 🎥Long Covid Advocacy💙
@LongCovidAdvoc
📘Legislate ⚕️Investigate 🌬️Ventilate 👥Educate Advocacy4 #LongCovid #MECFS #COVIDisAirborne Advisory Board Long Covid Support💙Patient Expert Group @TheWHNMark Vaughan
@Mark_C_Vaughan
Campaigning for migrant rights 🧡, environment & biodiversity, PR. Write a bit for @CenralBylines. LGBTQI+, disability, human rights. Views my own.Lewisham TUC
@LewishamTuc
Lewisham Trade Union Council - London email: [email protected]Alan Hall 💙
@alan_ha11
Trade Unionist. Campaigner. Personal account. https://t.co/I4v1imSOaARichard Amm ♿️🌍👨🦼
@Richard_Amm
Researcher, Designer, Engineer, Campaigner, Artist, Wheelchair user ♿: Disability, Design and Innovation MSc.Adam
@adammarshall68
there are places I’ll rememberBRIL
@BrilLiving
Bristol Reclaiming Independent Living. Grassroots Disabled people's organisation. #BLM #ChronicIllness #Disability #HumanRights #MentalHealth #NeurodivergenceonlyRants
@only__rants
just a girl that gets angry at the state of british politics | wishing for a kinder worldAnna Biggs
@WriteBiggs
Reader, writer, sleeper agent. Loves history, folklore & growing things. ME + expansion packs ADCI networkDr Jay Watts
@Shrink_at_Large
Consultant clinical psychologist/ activist/ neuroqueer bluestocking. Former Lived Experience Worker. Future failed poet. Will question ideology for cake.Nic
@MintGingerCraft
Political geek. She/her. Enjoy yourself, it's later than you think. Harry Leslie Smith @[email protected]𝕏istential ÂÛtist 🕊 ∞ 💛
@ExistentialAut1
Philosophy | Faith | Research | Advocacy | Art | Infinity | #ActuallyAutistic #AuDHD #Neurodivergence #MentalHealth #Disability #Love #Acceptance | 🕊 ∞ 💛Ableist Sisters
@NikkiGoldblatt
love photography, music, food, technology & archaeology. mum of three. unless a retweet, all photography my own work. She/herAisha Malik-Smith
@ANMalikSmith
@UniteLondonEast Regional Women & Equalities Officer. Cllr for New Cross Gate. Young Labour Disabled Officer. LFC fan. RTs/❤️s ≠ endorsements.🚩🤝Boog Winchester 🐟💙
@BoogWinchester
Irish/Canadian. She/her. Bi-Racial, Bi-Lingual, Bi-Polar. CSA survivor. Socialist. #BlackLivesMatter #TransLivesMatter #EveryChildMatters #StopAsianHate SPNFamMartin Arber
@thearbers
Ella-louise Bridenbecker
@Ellalouise96620
Grace
@kee75grace
Dances with Spiders🌎🇨🇦☮️🇵🇸
@lisaros33347477
Dem-socialist in the Elf-Help industry. Have ME/CFS-Long Covid ally Conservative free zone. Mask up for collective good. Trudeau rocks!Care4Christine
@Care4Christine
Campaigning for positive change. Everyone should be valued.KeepingHope95
@KeepingHope95
Disabled Advocate, Progressive Liberal, 💙🌈🏳️🌈🏳️⚧️ Exvangelical & Atheist #FBLC #EDS #LongCovid since 3/2020-pre-vaccine. #pwME ❌MAGA and ❌DM’AnitaTexasSunshine
@TexasSunshine18
searching medical scientific articles #MS #MECFS 38 yrs #AmpligenPatient #neuroimmune https://t.co/zygfECkRFa 🧬🧪 👒🐴🌵🌞🌎🍀💚💐 🏔️ 🌊 https://t.co/yU2SogQc19Sibylle Reith
@Komplexmedizin
MULTISYSTEM-ERKRANKUNGEN erkennen und verstehen - Über die unterkomplexe Wahrnehmung komplexer Erkrankungen. In jeder Buchhandlung erhältlich.Chanty
@Chanty37748606
Nav Shaikh
@shaikh_nav
Confirmed Diagnosis: -M.E.(cfs) 2004 -Mixed Connective Tissue Disorder -Lifelong Lupus(SLE) -Primary Raynaud’s -GERD -Klinefelter Syndrome & more!!Hannah Mcaleavey
@H_McAleavey
ESRC funded PhD student exploring the complexities of presenteeism and its impact on well-being among individuals with long-term health conditionszebra turtle
@chronicmelonic
paused neuroscientist | chronic illness & neurodivergence | #EDS #AuDHD | many years with #MEcfs worsened by #CCI, #PostVac, #LongCovid ...SarahParah ✊
@Sarah_Ward50
Mum / Socialist / CEV /Carer/Activist / crisp obsessed vegan / Children’s Rights Manager /She - Her 🌱✊ 🇵🇸🏳️⚧️Robin Avis
@RobinAvis115810
QuietStorm
@_Quiet___Storm
🧠∞♿ Long COVID 💔 ME 🔞 Scholar/researcher history/social 👩🏽🔬 Projects 🧰 🖤 Depresso ☕🖤 Invisible 👻 ⚠TW⚠️ Future SW🍑🕸️Dr.T, PhD I @remissionbiome
@chydorina
@remissionbiome helps people manage chronic illness Co-founder @remissionbiome https://t.co/K8MkrRMCcf https://t.co/Oy6IqjJywYJesse O'Mahoney
@jesseomahoney
Scriptwriter, songwriter, in a three year battle with long covid - if you're there too, I'm here for youFlor 🥀
@lugaresxcomunes
we need funding for research and treatments for Myalgic Encephalomyelitis and Long Covid NOW | #pwMECinnamon rolling along
@LongCovidFight
Prev LongCovid Fighter. Not much fight left. Supporting pw chronic illnesses, esp #LC #LongCovidKids #MECFS #PoTS #MCAS. #COVIDisNotOver #COVIDisAirborneDarlene
@long8darlene
Mark Kent
@MarkKent1043825
Brutus Berserk
@BrutusBerserk
Klaus Heffels
@DownloadArtAI
#MECFS, POTS, chron. pain. LC on top.Bell10. INFP. IQ151. Former C-level exec, living in darkness, silence and (brainfog)hell. Lang: DE-EN-NL #severeMEBlue Ghost - @DrArbor.bsky.social
@BlueGhost163
Retired Clinical Health Psychologist, Disabled #PwME Myalgic Encephalomyelitis for 30+ years & Syringomyelia. @DrArbor.bsky.socialManisha Mavani
@ManishaMavani
bethereificould
@bethereificould
A mirrorbox and map taking messages from people with ME/CFS or long COVID to places they love but can no longer get to #ACEsupported #socialart #missingmillionsRebecca Yeo
@disabmurals
focussing on disability, asylum, migration and wider social justice issues. Also may move to: @[email protected]Michael Witter
@witter_mic4953
Umweltschützer Naturschützer TierschützerLinda Morgenstern
@handcarryfilms
Artist/Activist Retired Docu Filmmaker due to #MECFS. DX 1990 post infectious viral syndrome. Never recovered. Severe Chronic Illness. Outreach to #LongCovid.Kathy D
@SlpBeauty333
I'm in LSG. You probably don't want to follow me if you don't like foul language. I haven't been on here since 2017? That can't...oh it's when celebs ruined itb-mwnci
@b_mwnci
🏳️🌈🏴🇬🇧Faithless
@FaithOxenbridge
Tired of defending my reality. Vax induced ME (still pro Vax) Bedbound. Not tired; sick. Used to write & teach. Here for the research and outrage.AloneLonghaulLady
@LadyLonghaul
animal adorer • impatient advocate • LC 2020 • masker • needs more spoons • prefers clean air • some adult language • #ADHD #HSD #spoonie #pwME #pwLCMedical mess
@longcovidpain
Iatrogenically harmed. Immune system gone mad.More Than 1 Forum (MT1F)
@MMt1f
Peer Support group for people with long-term comorbidities. Self- advocacy & advocacy. Shaping services towards a social model of disability & Mental Health.Rebecca Farren
@rebecca_15
Sociologist, researcher and pop culture nerd. Writing about disability, books and Doctor Who. 30. She/her ♿️ 🏳️🌈