Art on a Mission
@artmission
All proceeds from our store support people with #MyalgicEncephalomyelitis. Special orders, #art & #photography donations welcome. [email protected]
ID: 1084544331803848704
https://rdbl.co/2Do2lPy 13-01-2019 20:14:53
399 Tweet
489 Followers
914 Following
Tom Kindlon
@tomkindlon
With ME 36 years (30 yrs severe). 95% of posts on #MEcfs/#LongCovid/#chronicillness. 26 publications in peer-reviewed journals. @IrishMECFSAssoc trustee 28 yrs
Peter Julian 🇨🇦
@mpjulian
Candidate for New Westminster-Burnaby-Maillardville | Proud New Democrat 🧡
I am the ghost
@i_am_the_ghost
Try & change the world instead of just shouting at it. Vegan. Workers rights. Human rights. A fair days work for a fair days pay.
Cort Johnson
@cortjohnson
Founder of Health Rising /Phoenix Rising - Chronic Fatigue Syndrome (ME/CFS)/Fibromyalgia/Long COVID journalist/blogger - ME/CFS/FM patient for 40 plus years
@richardvallee.bsky.social
@richardvallee
I play language. Mostly irreverent. Debugger. AI. Global warming. Integrity. Healthcare. Science. We are actually in the pre-truth era. #MillionsMissing
Valerie Eliot Smith
@valerieliotsmit
Independent researcher living with myalgic encephalomyelitis (ME) since 1981. Barrister (ret'd) #TMTlaw Visiting scholar @QMUL Blog valerieeliotsmith.com
Bhupesh K Prusty
@bhupeshprusty
A passionate molecular virologist who believe in patient oriented scientific research. Using viruses to understand human existence. Science is for society.
Paula Knight
@paula_jknight
Author Artist THE FACTS OF LIFE (2017) Kidlit books x3 author. Writer, drawer, poetry, photography. Disabled. Bed-based 6+yr v severe M.E. #pwME (she/her)
Cat
@ecolocat
EcoloCat
Katie Bee🇪🇺
@katelinbee
Artist, Mother, Nature Lover. Living with and raising awareness of Post-viral Autoimmune/neuro-endocrine disease commonly known as M.E/cfs 10yrs+ @kateboyceart
Anil van der Zee ©
@anilvanderzee
Former professional ballet dancer | Bed/sofa-bound M.E. patient | Using Twitter to raise awareness for #MyalgicE | #IACC #art2cureME #pwme #millionsmissing
Dan Wyke 🦠➡️🧠🔥
@dan_wyke
M.E. inactivist, person-centred counsellor (see link), recovering poet (Rack & Waterloo Press)
Sabrina Poirier (On Hiatus) 🇨🇦
@sabrina_poirier
Community Builder / Passionate Collaborator / Chair - #MedicalEducation Group / #ResearchPartner / #MECFS #LongCovid Advocate / #PwME / #MCAS / #POTS / #Fibro
Dr Ellena Dee
@leggyjelly
AHRC-funded PhD @UniofExeter on conjoined twins in literature and film. Disability studies, embodiment. Chronically ill. ♿️ Poet. Nerd. Views own.
davidtuller
@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.
Open Medicine Foundation
@openmedf
OMF is fundraising to support open, collaborative research to find effective treatments and diagnostic markers for ME/CFS, Long COVID, and related diseases.
Katy B
@katybruce108
Myalgic Encephalomyelitis ME + POTS 38 years Donor to the @mecfsbiobank for 10 years & @DecodeMEstudy Please watch dialogues-mecfs.co.uk/videos/ #pwME
Cʟᴀᴜᴅɪᴀ Sᴄʜʀᴇɪɴᴇʀ
@claudespu
Seit 2008 an #MECFS erkrankt | Team #MillionsMissing Deutschland @mmissinggermany | Team #SIGNforMECFS | @fcunion
Phoebe Boag
@phoebsbo
Life is being autistic and chronically ill with ME and writing about it. Doodle artist. Smorky's human. She/her.
Rivka
@rivkatweets
Activist/Organizer: ChronicIllness, disability, ME/CFS, Lyme, LongCovid, women | Writer: WashPost, MarieClaire, NPR, Ms, Newsweek | Playwright: Many productions
Natasha Lee-Mays
@natashaleemays
Prophet ALP Sovereign Australian
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 🔬
PwME 4 bioMEdical research
@valebodi
Surviving #MyalgicE #AAG to tell the story, patient&advocate w/ a JD, into: MEdicine, Social justice & the Arts, Human neutrino/MEdical apolide/gnarled Pacer
#MEAction Network
@meactnet
A global network fighting for equality for Myalgic Encephalomyelitis. #MEAction #MillionsMissing linktr.ee/meactnet
Dr 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 ZIONISTS WILL BE BLOCKED
Anitra Cajander
@anitracajander
I am a 55 years old woman from Helsinki. I've been disabled after a car accident since -99 and suffer from #chronicpain #hypersomnia #braininjury severe #MECFS
Anny W.
@annyweatherwax
Psychotherapist, blending neuroscience, creative & trauma work. Living with ME. She/her.
Sheila M. Stefhon
@sweet_pea_315
Jesssica🖖🏻👁
@jessscia_
Your favorite super ⭐️ 😘💋
Billy Hanlon
@bhanlon15
ME/CFS | Long COVID | IACC
Jo
@cfs_jo
CFS(!) & POTS diagnosis, ME symptoms - trying to accept. Still me. Sense of humour intact. Proud “Anti-Recovery Activist” Mostly on justjo@bskysocial
MrsRobinson
@mrsrobi25154402
In the before I was a Bikram yoga loving commercial interior designer. #MEWarrior cucucachoo
Psychology Says
@lie2me___
Criminal Psych profiler, here researching my paper #Politicallyhomeless so I Lead with morals, principles & values
Nitor
@nit0r
Modern day philosopher, entrepreneur. I'm currently writing ✍️ my first book - a sci-fi trilogy about society in 2822 - 🤖📚📖. Thank you for your support! 👏🙏
bad_sleeper
@heavyrester
Was super single dad & active computer geek. Attempting to manage my ME :-(
Thomas Heinzmann
@thomasheinzman_
I got a virus & never recovered | EBV 1985 & Influenza 1989 #MECFS | Kämpft low dosed für Aufklärung, Anerkennung, Versorgung & Forschung.
FUTURE4HEALTH EU/USA
@future4h
♦️Top quality #BEYUNA 💯% natural SUPPLEMENTS #CLEANLABEL #NoChemicalAdditives #VEGAN #NoGMO ♦️ZOYA distr for EU #big10free nailpolish/lipstick. ME/LYME patient
Mariechen
@mariech17758467
ME /Cfs Kämpfer sat1nrw.de/aktuell/leben-…
ME/CFS Münster
@cfsmunster
just another #pwME living in Münster | disabled by #MECFS | mecfs.de/was-ist-me-cfs/
Anita Willams
@anitawillams10
EDSer
@edser53874642
Becky Holmes hates spinach
@deathtospinach
I only date celebs (inc. Keanu, Brad, Neeson, Jagger & Prince William), brave US peacekeeping soldiers in Syria or oil rig workers. First book out now 🎉
Mavie
@2_set_me_free
one of the #millionsmissing with #severeME
Valeska Tietze
@val_140137
Covid Long-Haulers Support Group Canada
@longcovidgroup
🇨🇦's Largest Long Covid Community over 20K Advocating Recognition Research Resources Lead Rep of Long Covid Kids Canada @LCKCanada
PolyBio
@polybiorf
501(c)3 transforming how #LongCovid, #ME/CFS & Lyme+ are studied, diagnosed, and treated. Leading the #LongCovid Research Consortium.
Edna, M.E.Advocate 🇨🇮
@ednamacnamara
💙 M.E.Carer/Advocate of son aged 31, ME,11yrs 💙. RaisingAwarenessFor #PwME #Carers #LC #findAcureME #greatestMEdicalscandal ednamacnamara.bsky.social
Kerstin
@kerstin_mecfs
ME since 2009 -Bell 20- I want my life back! #mecfs #POTS #lipoedema #acneinversa #SFN #Fibro #HDS #ADHD #MultipleChronischeViren #EBV #CMV #HPV6
European ME Coalition (EMEC)
@emec_advocacy
Advocacy organization for ME/CFS patients and their carers in Europe
Rebecca Carr
@rebecca46824142
Venny
@art_ptah
20 | Traditional and digital illustrator and graphic designer | DMs open - always happy to chat | anxious art student
Cyrus | Mastodon in bio
@cyruxime
Energetically compromised by severe #MECFS. All systems operating at minimum capacity & overloaded. he/him. On the Fediverse: @[email protected]
#GeneralStrikeAgainstFord
@strikeford
Pissed Off Ontario Armchair Warrior Sick and tired of the Conservatives Could always use some help with cost e-transfer: [email protected]
Bavardlyn
@bavardlyn
Opinions my Own Board member at ME-international. Just doing the best I can with what I’ve got! #pwME me-international.org
Doctors with M.E.
@doctorswithme
The global professional association for medical practitioners, scientists and researchers in the field of #MECFS, #LongCovid and related postviral disease
▪︎ art ME cfs 🎗
@artmecfs
#art𝗺𝗲cfs • sharing art created by #𝗽𝘄me 🢐 🐳💤 #mecfs #chronicpain #chronicfatigue #artistonhiatus #meawareness #rememberme #disabledartists 💜
linda sepp
@lindasepp
Seriously 'Sensitive' to Pollution, LongHauler, MCS/ES, FragranceFree access, inclusion, HumanCanaries, EnvironmentalSensitivities, EnvironmentalHealth
FraudListing
@fraudlisting
Redditors against pseudoscience | Fraudlisting is about exposing unproven and nonscientific treatments for myalgic encephalomyelitis (including Long Covid)
Chronic Illness Channel
@chronic_channel
Youtube channel covering Chronic Illness, Universal Basic Income and Air Pollution. @chronicchannel.bsky.social Threads: @chronic_channel
Hidden Disability Symbol Canada
@hdscanada
Join the movement for a Hidden Disability Symbol in Canada. It's time. It's right. It's needed. Visit the link below to become and ally and join the movement.
Peta
@petamarilyn
#MECFS for too many years! * I’d love my active life back! 🙏🏻💙🌊 * Somehow I still have hope! * You can help #pwme @EmergeAus & @OpenMedF
AngME#FBPE#FBPA#RNLI#BLM# FBPPR#
@22angelaharris1
pwME#Starmer if he supports rejoin EU
Carole Bruce
@carolebruce17
💙Art, Nature, Books, Some Music. Severe ME 32 years. Daughter severe 38 years. Furious about treatment of ME. bsky.app/profile/cabruc…
Russ Moorhouse
@amountainbivvy
Account no longer used, I am on Instagram @amountainbivvy 🏔️⛺⛰️ Fell Asleep on lots of mountains ---- columnist for @trailmagazine
Emma-Louise
@rumeloise
Bi, atheist, suffered from M.E for 20yrs now. Interested in raising awareness of the injustices surrounding M.E.