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
John Peters
@johnthejack
Unbeliever (political & relig), Wales rugby, #c4news, porridge, #MEcfs johnthejack.peters johnthejack.com
Deb Meades 💙
@dameades
Previously nurse, presently wife , Grandmother and mother. Currently in limbo due to M.E. and Fibromyalgia.Obsessed with books
@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
Emma, thechronicsurvivor✨🕯
@chronicsurv1vor
Aspiring Author ✍🏼📖 |Singer/Actress, Trainee Therapist on hold due to #MECFS ♿️ for 6 years | #POTS / #IST✨Spiritual Awakening. Lessons from the void. 💖
It's M.E. Kathryn
@joyk8
Medically retired RN, #pwME since 2001. #POTS, #EDS, #MCAS, #DDD JoyK8.bsky.social
Pathogen Hunter
@lymehater
Lyme disease advocate, tennis player, biomedical researcher, skier, reader, gourmet cook, antique hunter, world traveler, geek with varied interests.
Bateman Horne Center
@batemanhorne
Bateman Horne Center is a non-profit medical, research, and education center devoted to eradicating ME/CFS, FM, Long COVID, and related conditions.
Cantina Hitchin
@cantinacarnitas
Award winning griddled burritos, tacos, nachos and quesadillas being served from our Hitchin Cantina! Fiesta Garden with plenty of Yum & Bass
Dan Wyke 🦠➡️🧠🔥
@dan_wyke
M.E. inactivist, person-centred counsellor (see link), recovering poet (Rack & Waterloo Press)
Katherine Reynolds
@kreynoldswriter
Daniel Moore
@talmandaniel
Curious & exhausted peace seeker, co-host of @pempodcast23, photographer and blogger. PwME, sidelined social worker, grief dealer, joy peddler, SAFC fan, He/Him
Alisontomyradioooo
@arisonsned
@arisonsned.bsky.social Cat and Dog botherer. YP counsellor retired. Want my bike and my health back 🩵
Susan Kandarian
@susan_mecfs
Professor-scientist disabled due to worsening #MECFS. Ally for ppl with infection-associated chronic conditions. #longcovid 🏳️🌈
Alex Struck
@alex_struck
Tired mama warrior, latte junky, irrepressible baker, word nerd, eternally seeking out the sacred and the scarred
julia lee
@julialeelee777
I'm a Christ follower, wife, mother, RN,and thankful for the blessings I've been given. Constantly battling ME. RT/follow doesn't always=alignment
Rev. Maria Pierre
@losdocepasos
ME (Chronic Fatigue Syndrome) Warrior, Interfaith Minister-Retired, A Course in Miracles Teacher, Encourager, Advocate. TCM lover
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
samee
@sam0988217119
Home is not where you are born, but where you feel alive...Wherever there is justice, there is home🍁 ......Canada the Dream
N🤗VA ME-CFS/POTS/LC/FMS etc Support Group
@cfsnova
For pw/caring4 long haulers: ME/CFS/FMS; Orthostatic Intolerance, POTS; Long Covid; Chronic Lyme. VDR immunopathy. MTHFR+. MCAS. By @NovaSupport Elly Brosius.
Susannah H
@firebug70
Mum. Carer for my son. Former English teacher. Holding on to hope. Researching #Lyme #ME #LongCovid #Pandas #Pans
KK
@ksannara
#ME #MECFS #LongCovid #BildungAberSicher #Petition #MECFS. ➡️SIGNforMECFS.de ⬅️
Laura CrowFella🌻🇺🇦🇮🇱🇱🇹🇺🇸
@elvee57
Former art therapist, musician, ocean lover, advocate for truth about M.E., #NAFO Fella, No DMs, Slava Ukraini!
Suzan Jackson
@livewithmecfs
Writer with ME/CFS & Lyme & son w/#MECFS & #Lyme; love to travel, read & spend time outdoors w/family & friends; write 2 blogs & author of chronic illness book.
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 🔬
Vix Edwards
@fuglymanorart
• SPMS & Fibromygia • determined to be my true authentic self • Sharing unique happenings of my life & MS • Self love advocate • INSTAGRAM: yogivix
#MEAction Network
@meactnet
A global network fighting for equality for Myalgic Encephalomyelitis. #MEAction #MillionsMissing linktr.ee/meactnet
Mary Smith
@marybjsmith
Views are my own.
Warp Speed for a LC/ME cure
@corinap19
Despondent over the political and social handling of the pandemic and its victims
Tina Rodwell #TeamPatient🇺🇦🕊🌎🕊💞
@tinarodwell1
They called us activists 🤦♀️ I wear that slanderous name calling with pride for all the #MEheroes out there Fighting for my #MEhero son #TeamPatient💚
Gottfried Weibler
@goddyw567
Formerly CIO / Group IT Director, now on sabattical leave / retirement due to #MECFS
Billy Hanlon
@bhanlon15
ME/CFS | Long COVID | IACC
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…
Marky Mark
@mrkstdngr
#ME #CFS #CCI #POTS #MCAS
Dr. Daniel Loy
@loy_daniel_de
Ehemann, Jurist. #MECFS. Team #SIGNforMECFS. Team #GOfundMECFS. One of the #MillionsMissing.
Adam
@abrokenbattery
Severe ME patient currently on a 10% battery, the gas goes out more than I do. I also compile ME/CFS Awareness videos.
Ben H
@benh_mecfs
ME/CFS patient advocate, @OpenMedF science correspondent. Bedbound. Former biochemist in training, physiology, powerlifter, PT/gym manager. Musician. F1/Boxing.
Illustrator Interrupted
@franceyme
amandafrancey.com illustrator, amateur photographer and bird telepath. Advocating for myalgic encephalomyelitis #MECFS #LongCovid @franceyme.bsky.social
MECFS Stuttgart
@mecfs_stuttgart
Informationen & Aufklärung über #MECFS und #LongCovid 🇬🇧🇩🇪
#NotJustFatigue
@njfatigue
We are a 501(c)(3) sounding the alarm on ME/CFS through digestible, creative content. This is #NotJustFatigue. Donate today👇
Elizabeth Ansell
@elizansell
Founder + Executive Director @njfatigue. Previously at Showtime and ABC News, among other places. Quit job due to #MECFS. This is #NotJustFatigue.
Sharon Cohen
@sharonc97936831
Teresa
@valles1teresa
Klaus
@bedridden_hero
#MECFS, #POTS, #MCAS, #SFN, chron. pain +PostC. Bell0.PG4. INFP. IQ151. HSP. Former highperformer now 24/7 bedridden. Lang: DE-EN-NL #verysevereME #pwME
Petra
@petra_v_3l
#AllTogetherWeBattle_InvisibleDiseases #B12 🩼🩸 #ME🩵 #FM 💜#Glucoma Advocating for understanding nothing more!
bethereificould
@bethereificould
A mirrorbox and map taking messages from people with M.E. or Long Covid to places they love but can no longer get to #ACEsupported #socialart #missingmillions
Walk for M.E
@walk_4_me
Official Walk for ME Twitter account. Email: [email protected] FB: facebook.com/WalkforMEUK/ Instagram: @walk_for_me_
RTHM
@rthm_health
RTHM connects you with a digital care team specializing in Long COVID and ME/CFS that provides access to a range of therapies based on the latest research.
Ev Ryan
@ryan8ev
lynne disabled
@disabledlynne
Never give up always smile share positivity all the time living with a disability
VotingGenie.Com
@votinggenie
Voting Genie is a Super Pac dedicated to change how our health system inhumanely deals with those who suffer from chronic pain. Please follow so we can win this
Sarah O'Connell
@sarahoc_mecfs
#pwME patient 12 yrs & mum of 2 with ME, #LongCovid & PANS • ME & LC Advocate • Co-Founder LCAI • Women's Health; Endometriosis,PMDD • Sci-fi & movie lover
Long Covid Kids Rep.of Ireland 🇮🇪
@lckireland
LCK & Friends Ireland, Associate Acc @longcovidkids. Advocacy & support for kids with #PostViralKids #LongCovidKids #LCKfriends 🧡🧡
ME/CFS & Long Covid Ambassadors
@mecfsambassador
A community of Ambassadors and Advocates helping connect patients and their families to resources and support!
T
@nofo__allmo
Queen of Vertigo👸Empress of Brainfog👑Wanderluster Interrupted🌎Inconsistent Gardener🌱#SevereMECFS #MigraineWithBrainstemAura #VestibularMigraine +etc,etc🙄
Kara
@thebabalicious
A diary about living with fibromyalgia.
AngME#FBPE#FBPA#RNLI#BLM# FBPPR#
@22angelaharris1
pwME#Starmer if he supports rejoin EU
Nicole Lange🇨🇦
@nicolel42759817
Grandma to pups Grizzley & Cedar, and Scruffy, animal lover, a positive person. Can’t have my own pets due to allergies, ME/CFS, fibro, POTS, MCAS…
Chrissy Clements
@clementschrissy
Hi, I'm Chrissie, have been an ME Warrior for 7 years this November. Am a huge Jason Hughes fan he's gorgeous. Love Hollyoaks, EastEnders and Emmerdale ❤️💕🥰
#MillionsMissingDenmark
@millionsmissin2
Emma Wooller
@woolleremma
I told you I was ill.
The OutlawTorn
@outlawtorn92
Old, bald, fat, misanthrope and winner of the crappy disease lottery three times! (M.E Myalgic Encephalomyelitis and a Degenerative Spinal Disease & arthritis)
Annette Streich
@annettestreich9
ME/CFS , POTS and fibromyalgia . Love food , foreign films and my wee Siamese beasties .Once was witty now happy if I can form complete sentences 🤪
HealthfulStories
@healthfulstori1
Non-Profit. We magnify your health journey to help others. HealthfulHeroes.com/New-Journeys/ Sharing your story can heal: [email protected].
🇨🇦Ryan Lythall - Rolling Enigma♿️
@rolling_enigma
Weekly Columnist at Ottawa Life Magazine. @ottawalifers Check out my linktree page. Tweets & Retweets are my own.
The Chemical Sensitivity Podcast
@podcastingmcs
Podcast amplifying voices of people with Multiple Chemical Sensitivity (MCS) and research about the illness. Subscribe where you get your podcasts! 🎙️🎧✨
Massachusetts ME/CFS & FM Association
@massmecfs
To improve the lives of all people affected by ME/CFS and Fibromyalgia through advancing awareness, care, treatment and research.
Joseph Falzone MD
@josephfalzonemd
A physician with interests in neuroscience, psychiatry, chronic pain, and many others
linda sepp
@lindasepp
Seriously 'Sensitive' to Pollution, LongHauler, MCS/ES, FragranceFree access, inclusion, HumanCanaries, EnvironmentalSensitivities, EnvironmentalHealth