Alice Maria
@alice_maria28
#pwME and long time sufferer of #endometriosis 🌻 #adeno & #crohns
Dog nerd 🐕 #adoptdontshop
#myalgicencephalomyelitis
ID:1245700433529667596
https://www.instagram.com/__amaria_/?hl=en 02-04-2020 13:13:13
857 Tweets
431 Followers
617 Following
Katy B
@KatyBruce108
Myalgic Encephalomyelitis - M.E + POTS 38 years Donor to the @mecfsbiobank & @DecodeMEstudy Please watch https://t.co/rPfzhZQ6po #pwME
Lizzy H
@hopefullizzy
29y/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✨
Jo
@cfs_jo
CFS(!) & POTS diagnosis, ME symptoms - trying to accept. Still me. Sense of humour intact. Proud “Anti-Recovery Activist”
Naomi Harvey PhD #WearAMask
@Naomi_D_Harvey
Zoologist. She/her. 22yrs with ME/CFS. Pro-vax but vaccine injured. Life on pause (views my own - unemployed) ♿️ https://t.co/YeMrEWwEg5
Dan Wyke 🦠➡️🧠🔥
@Dan_Wyke
M.E. inactivist, person-centred counsellor (see link), recovering poet (Rack Press, Waterloo Press)
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 🔬
Dr Claire Taylor
@drclairetaylor
Doctor|Special interest in Long Covid,POTS,ME/CFS&MCAS| neuroscientist🧠Long Covid kids champion|WHN expert advisor|long Covid clinic🏴Views my own
Carole Bruce
@CaroleBruce17
Severe #ME for 32+ years. Ex- psychotherapist. Daughter, severe ME 38 years. Eldest son, MS. Apart from that ❤️Art, people,nature, books, some music.
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.
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
It'sME(Jaime)
@exceedhergrasp1
Director of Sci & Med Outreach, #MEAction Stanford Med TIME100 Health 2024 #ME, #EDS, #POTS, #LongCOVID Views my own [email protected]
Phoebe Boag
@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.
Thane Black
@thane_black
'Kindly let me help you or you will drown said the monkey putting the fish safely up a tree' #SevereME
Alisontomyradioantirecoveryactivist
@arisonsned
Anti Recovery Activist of 30 years prior to Social media. Always support Biomedical research. Prove it 😘 Cat and Dog botherer. YP counsellor. Want my Bike Back
Janet Dafoe
@JanetDafoe
Caregiver for very severe ME/CFS son, advocate and fundraiser for End ME/CFS PROJECT at OMF and CFSRC at Stanford. The rest of my life is on hold...
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.
Marky Mark
@MrkStdngr
#ME #CFS #CCI #POTS #MCAS
Crafty Miss
@CraftyMissB
I'm Beth, embroidery & craft are my buzz. #socialist #pwme #disabled insta: thecraftymissb https://t.co/H4UqOa9igd
Martin Hippe
@pausedME
East Westphalia by Nature ⎮Lawyer by Profession | #MECFS activist | @Mirame_Arts | No medical advice!
Tom Kindlon
@TomKindlon
With ME 35 years (29 yrs severe). 95% of posts on #MEcfs/#LongCovid/#chronicillness. 26 publications in peer-reviewed journals. @IrishMECFSAssoc trustee 27 yrs
Angela Reiersen, MD, MPE
@AngelaReiersen
Associate Professor of Psychiatry @WUSTL ; Opinions are my own; Tweets are not medical advice. Say my name: https://t.co/4CbvdgvJC8
Cinnamon rolling along
@LongCovidFight
Prev LongCovid Fighter. Not much fight left. Supporting pw chronic illnesses, esp #LC #LongCovidKids #MECFS #PoTS #MCAS. #COVIDisNotOver #COVIDisAirborne
Melissa Mazur
@PhillyPhile215
Just a Philly girl, livin' in a lonely world…and a Luddite learning to Twitter. #LongCovid since March 2020 || Lawyer on Pause
Chronicillnesswarrior1 ♿️💙✝️💟
@fionangreg
Wife, mum, pwSME/CFS, FND, Fibromyalgia Observe small things, don't rush, love & forgive ❤️ #chronicillnesswarrior #loveyourself #loveothers
Heath
@MEawareness
#MyalgicEncephalomyelitis(M.E) sufferer. I had a virus & didnt recover. Are questions usually rhetorical? I cannot give blood, ever: https://t.co/tU1sspbOiU
Canary
@TheCanaryUK
The Canary. Disrupting power since 2015.
sharon askew
@88888888881
G R A C E 🌸
@withgrace___
🥀 severe ME/CFS mama to baby son ❤️ heart full, body broken 🌻 INFJ
DHARANA
@dharana_shiva
#EMsfc muy severa Bajo un techo como Cielo Pensamientos Vida
Dr Nicola Clague-Baker
@ClagueNjc36
Physio @LivUni co-founder @physiosforme | PhD | neuro rehab/ex physiology/fatigue/healthy lifestyles/mental health/ME/Longcovid/EDI/all views my own she/her
Leonie Potgieter
@Despicable_M_E
Living with M.E. as best I can. Love nature, humans not so much.
Fran Haddock
@franhaddock_
Spoonie 🥄 Activist ✊ Vet 🩺 (she/her) Currently bedbound with severe ME + Long Covid (more active on IG)
🌻Kirsty
@Kirstycfsmelife
CFS/ME 15+ years and POTS 🐼 trying to improve my health and one day fully recover
#NotJustFatigue
@njfatigue
We are a 501(c)(3) sounding the alarm on ME/CFS through digestible, creative content. This is #NotJustFatigue
Amy
@alexandrite113
Long Covid to very severe ME/CFS to mod/severe ME/CFS. Tweeting into the void. DX'd autistic ✨
Sharon Cohen
@SharonC97936831
#TwitterHaiku; Tulane MBA; LSE; Univ of Wisc Mad; former career financial services; international bus. #chronicillness; #physicaldisability.. 4 NIH studies
Brad
@AutonomicBrad
Bachelor of Biological Science Degree. #LongCovid #TeamAutoantibodies #Bc007. Any tweet is my opinion and not medical advice. Check out my podcast on Spotify
Larry Weis
@LarryWeis7
#ME/CFS,#SFN,#Dysautonomia Owner-Commercial Insurance Agency
oliver benson
@olliebenson_
elle carnitine 🍉
@elle_carnitine
🪳
Ramy2.0
@Ramyisback
I am back from the twitter grave, with memes, and other stuff about mecfs and long covid.
Leonard Jason
@CenterRes
Leonard Jason is a Professor of Clinical and Community Psychology at DePaul University. He is also Director of the Center for Community Research
Elizabeth Ansell
@elizansell
Founder @njfatigue. Previously at Showtime and ABC News, among other places. Quit career due to #MECFS. This is #NotJustFatigue.
KK
@KSannara
#ME #MECFS #LongCovid #BildungAberSicher #Petition #MECFS. ➡️https://t.co/EuFUEYyf9j ⬅️
HopeStarMasacre
@MscreStarHope
its alright… im just dying is all…// writer and performer of the theatric kind // disabled as fuck with #LC #ME #POTS #MCAS & more // antizionist ✡️ 🇲🇽🏳️⚧️
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.
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! Chronically Surviving
@Chronically2784
Queer & Disabled. ME, POTS, Ulcerative Colitis. (she/her)
John Cusack
@johncusack
Apocalyptic shit disturber & elephant trainer. Justice for all - or no one. A retweet is not an endorsement - SEEK TRUTH SPEAK TRUTH LIVE TRUTH .
Novara Media
@novaramedia
📺 📰🎙🚩 People-powered media. https://t.co/i6f8cZyfGr
Ghassan Abu Sitta
@GhassanAbuSitt1
Plastc & Reconstructive Surgeon Founding Board member @INARAORG. RTs are not endorsements
MoTaz
@azaizamotaz9
A genocide survivor, Trying to tell more
Dena Takruri
@Dena
Peabody Award-winning Senior Presenter @ajplus | Coauthor of They Called Me A Lioness: A Palestinian Girl’s Fight For Freedom out now! https://t.co/49V6jC0fvX
Israel Defense Forces (Parody)
@IsraelDefenseF
Israel Defense Forces Parody Account. Satirical commentary. Don't take seriously. This account does not represent the IDF or Israel. Backup: @IsraelOffenseF
Max Blumenthal
@MaxBlumenthal
Editor, @TheGrayzoneNews
Abby Martin
@AbbyMartin
Journalist @EmpireFiles, #GazaFightsForFreedom, https://t.co/qgo82edlsE
Rania Khalek
@RaniaKhalek
Journalist and host of Dispatches on @BTnewsroom.
Kendra F
@SurvivingCFS
Disabled for a decade due to MECFS | recently escaped homelessness | I’m advocating for those who can’t | DM for merch orders.
Mish
@Shelmish
💙#pwME and #fibromyalgia since 2020 w/o any clear trigger. currently housebound. also enby and ace 🏳️🌈 any pronouns 🇵🇸 @shelmish.bsky.social
Bassem Youssef
@Byoussef
political satirist,vegan,documentary :tickling Giants,book: revolution for dummies instagram: https://t.co/mtJB6E7ZZb official facebook below
Ava-Santina
@AvaSantina
Political Correspondent @PoliticsJOE_UK @JOE_co_uk | Formerly @LBC | Instagram @avasantina_
A 😎 Long Covid + MECFS Billboards
@AaronCa11
@lcmebillboards https://t.co/0rnAQeYP77
me_ots
@te_rztoo
ME/CFS (chronic fatigue-syndrome) since 2018/19. We need basic + therapeutic research ! #PEM
erica
@sadfoxqueen
25 💜 chronic lyme and autistic girly ☀️ still masking 🖤 miss gonna be alright someday
Nav Shaikh
@shaikh_nav
Confirmed Diagnosis: -M.E.(cfs) 2004 -M.C.T.D. -Lifelong Lupus(SLE) -Primary Raynaud’s -G.E.R.D. -Klinefelter Syndrome -P.E.G. feeding tube (July 2023) & more!!
AnitaTexasSunshine
@TexasSunshine18
searching medical scientific articles #MS #MECFS 38 yrs #neuroimmune 🧬#HHV6 #EBV #lowNK #blockallbots🧪👒🐴🌵🌞🌎🍀💚💐 🏔️ 🌊
Corey Byrd (Severe M.E - Bedbound)
@Th3birdman333
V severe #MECFS; 99% bedbound. All #pwME are warriors. Warriors need sword/shield/armor. Let me be your armor with advice. Let me be sword/shield by advocacy.
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 #missingmillions
Patchwork Paws
@PatchworkDogs
We promote responsible dog ownership with a particular focus upon new rescue dog adoptions. Our website & articles are completely free to view. 🐶🐕🦮🐕🦺🐩
A Rose By Any Other Name
@g0th1crse
Trans MECFS ASD fag. “Everything is impossible until it happens.” Multiple/#pluralgang. . Future Polygamist. Misandry Empress. she/they. PM for alt