@marshadecordova.bsky.social
Labour MP for Battersea, Balham & Wandsworth [email protected] https://linktr.ee/marshadecordova1
@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
@camillebuckner.bsky.social
My pen is huge and I love sentences. And words. Like wombat and elixir. People and planet over profits. Build new systems. Equity. Inclusion. Justice. #BLM #LandBack #DefundHate #LongCovid (3/2020) #MECFS #Poetry #AcademicSky
@phillyphile215.bsky.social
Just a Philly girl, livin' in a lonely world…and a Luddite learning (now) to BlueSky. #LongCovid since March 2020 || Lawyer on Pause
@momazonrises.bsky.social
🚫DMs / 🌊🌊🌊 / DO NOT OBEY IN ADVANCE / #ProudBlue / #DemocracyWarriors / #BlueSkyResisters / anti-racist / LGBTQIA Ally / Pro-Choice / 🚫MAGA / Chronic Illness Advocate / #MECFSWarrior
@timallwood.bsky.social
Low-carbon living & birding in TG42, East Norfolk. Patch 327, finds 301, patch finds 286. Teacher. Football, music, guitars, lurchers. Flight-free for 18 years 😁 https://tg42lowcarbonbirding.wixsite.com/tg42 Hardcore will never die, but you will.
@mattp1975.bsky.social
North Warwickshire birder - mainly on foot or by bike 🚲🦉🐦⬛🦆🤓 IT engineer💻 | metal vocalist 🎤 | gardener🌻| jogger🏃♂️| Green Party member🟢 #birdingbybike #lowcarbonbirding #warksbirding #ukbirding
@madknittrsteaparty.bsky.social
Love crafts, history, stories, natural world & spending time with husband, children, family & friends. When M.E /CFS & POTS doesn't stop me - which is most of the time right now. Usually found in a dressing gown. Devon, UK ♿🌿🏳️🌈🏳️⚧️🇺🇦
@shrinkatlarge.bsky.social
Consultant clinical psychologist/ activist/ neuroqueer bluestocking. Former Lived Experience Practitioner. Future failed poet. Will question ideology for cake. 💜🎭🦓🥄🏳️🌈 #MadSky #TraumaNotPD #Disability #Neurodivergent #Mad https://t.co/83d2Ztwpp2
@chronicpain247.bsky.social
I’m a wife and mummy, disabled spoonie 🥄chronically ill, trying to advocate for remote work for disabled people in media 🫶♿️
@ceri-turns.bsky.social
Politics - Eco-Socialist🍉 Green Party💚 (GPEW🏴🏴) Nature & Climate🌳 Social Justice⚖️ Covid Vigilant😷, Chair #GreensAgainstCovid (opinions my own) Feminist♀️Bi🏳️🌈 🇵🇸🇺🇦💃 🌍Lancaster, Lancs, NW 🏴 UK. 💆🌱👣Massage & Holistic Therapies at http://holistyx.blogspot.com/
@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!
@colleensteckel.bsky.social
Advocate for #MyalgicEncephalomyelitis using ME-ICC. Contracted ME in 1989 Substack: https://colleensteckelmeiccinfo.substack.com/ Volunteer at www.MEadvocacy.org Aspiring writer of paranormal fiction
@plantspetspics.bsky.social
I’m a disabled person (ME/CFS, LC, MCAS, hEDS, POTS, etc +++) distracting herself, when able, with plants, pets, photography, crafts, reading, trinkets & treasures
@litsadremousis.bsky.social
ALTITUDE SICKNESS (Future Tense Books). Upcoming: FIRE IN THE HOLE: A EULOGY FOR THE LIVING. Left WaPo b/c of Bezos. Esquire, NY Mag, PW, The Blvr, NPR, NYT, P&W, The Rumpus, McSwy's, et al. Cohost of PEM Pod. #pwME in #Seattle. https://litsadremousis.com
@katybrc.bsky.social
Myalgic Encephalomyelitis - M.E + POTS for 38 years Donor to the UK MEcfs Biobank for 10 years & @DecodeMEstudy Please watch http://dialogues-mecfs.co.uk/videos/ London, UK No DMs please #pwME
@michaelnobbs.bsky.social
Artist and tea drinker living on a hillside in Wales. Learning to live a gentle creative life and encouraging others to do the same. Diagnosed with #MECFS in 1997. www.patreon.com/gogently https://linktr.ee/michaelnobbs ✍️🧶
@chembarathi.bsky.social
AuDHD, CPTSD (she/they) ~Bangalore,India ~ Maker of beautiful things 🧶( #Knitting #Crocheting) Bedbound by #MECFS now Buy my art https://chembarathicrafts.mini.store support me https://ko-fi.com/chembarathi
@tomkindlon.bsky.social
95% of posts on #MyalgicEncephalomyelitis, #LongCovid or #chronicillness. With ME/CFS 36 years, severe ME 30 years. @IrishMECFSAssoc trustee 28 years 26 publications in peer-reviewed journals Social media: https://me-pedia.org/wiki/Tom_Kindlon
@kirsties.bsky.social
UK #pwME #pwLC #MECFS #LongCovid #PEM (post-exertional malaise) as well as #Politics and other related chat. I use lists to manage my chats here. Feel free to use them or ask to be added https://writingandme.com/
@rebellionista.bsky.social
Single mum. Expert napper. Pet wrangler. Severe ME/CFS. My son & I are AuDHD. Former gifted child. Reformed TV producer. Live for horror movies. Life is a roller coaster.
@brokenwingpoet.bsky.social
Poet. Writing on disability & eco justice. Bedbound with Long COVID and Severe ME. 🍉 🇵🇸 🌲 🐦 😷 #millionsmissing #disabilityjustice
@meactnet.bsky.social
A global network of people empowering one another to fight for equity for myalgic encephalomyelitis. Home of the #MillionsMissing linktr.ee/meactnet #pwME #MyalgicEncephalomyelitis #LongCovid #MECFS #ChronicIllness #DisabilityJustice
@nikosuvisto.bsky.social
Life on hold by severe #MECFS, currently 99% bedbound 🛌 Documenting my life like it is now, advocacy through photography 📷 📍Finland https://www.aquietstorm.me
@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.
@dialoguesmecfs.bsky.social
https://www.dialogues-mecfs.co.uk Website with videos created by Natalie Boulton & Josh Biggs with a Wellcome Public Engagement Fund Award. Professionals and patients explain key aspects of #ME/CFS and a longer film explores the wider context and history.
@mecfsskeptic.bsky.social
Exploring the history of psychosomatic medicine and research on myalgic encefalomyelitis/chronic fatigue syndrome (ME/CFS). https://mecfsskeptic.com/
@irishmecfsassoc.bsky.social
Irish Myalgic Encephalomyelitis/Chronic Fatigue Syndrome Association NB: Posts should not be considered advice Registered Charity Number 20100254 CHY 22039 #MyalgicEncephalomyelitis #ChronicFatigueSyndrome #MEcfs #CFS #PwME. Some #LongCovid items also
@me-cfs.bsky.social
Disabled by very Severe Post-COVID ME/CFS. Not always able to use phone. Bedridden. Unable to Speak. I care. My ME/CFS News Aggregator: @me-cfs.mastodon.social.ap.brid.gy Ⓐ💚, (FR/DE/EN, but posts in english) Clinging onto the ledge above the abyss.
@crankyqueer.org
#Queer and #trans #disabled people have always had to find new paths for our survival #Illder storyteller and strategist: http://thecrankyqueer.substack.com #PandemicsAreChronic ❤️T4T❤️Mask4Mask❤️ #FBLC
@chronicillnessmeme.bsky.social
Just a place where a bunch of chronically ill peeps can come to laugh through the pain together and maybe earn some extra spoons 🥄 instagram.com/chronicallyillmemes
@chronicchannel.bsky.social
Youtube Channel covering Chronic Illness, Universal Basic Income and Air Quality. https://www.youtube.com/@ChronicIllnessChannel Clean The Air http://bit.ly/CleanTheAirUK
@chronicillness.bsky.social
Chronic Illnesses + Autoimmune Disorders R no laughing matter but my humorous posts will make U feel better for while. https://chronicillnesstees.etsy.com https://mybodyistryingtokillme.com/ https://www.redbubble.com/people/ChronicillnessT #chronicillness
@ukdishisthub.bsky.social
UKDHHH is a network to allow those interested in Disabled, Neurodiverse, & D/deaf histories, from the ancient world to the modern era, to connect & collaborate. We are open to researchers, archivists, museum professionals, activists & everyone in-between.
@disrightsuk.bsky.social
We one of the UK’s leading Disabled People's Organisation run by and for Disabled people, working for justice and equality for all. https://linktr.ee/disabilityrightsuk
@bsky.app
official Bluesky account (check username👆) Bugs, feature requests, feedback: [email protected]