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 #pwMELizzy 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✨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/YeMrEWwEg5Dan Wyke 🦠➡️🧠🔥
@Dan_Wyke
M.E. inactivist, person-centred counsellor (see link), recovering poet (Rack Press, Waterloo Press)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.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/HimPhoebe 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.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 #MCASPaula Knight
@Paula_JKnight
Graphic memoir THE FACTS OF LIFE (2017) Kidlit books x3 author. Disabled. Bedbound 6yr v severe #pwME Submerging writer. Total Bedass. Print Disabled she/herME Foggy Dog 💙
@MEFoggyDog
Award-winning #socialenterprise in #UK. Working for #socialchange for the #MECFS community. Linktree - https://t.co/TNEwofcNnmBilly Hanlon
@bhanlon15
Director of Advocacy & Outreach, Minnesota ME/CFS Alliance | Long COVID AllyAmy
@alexandrite113
Long Covid to very severe ME/CFS to mod/severe ME/CFS. Tweeting into the void. DX'd autistic ✨lissa
@melissabreenx
writer of unfinished novels. disability advocate. chronically ill. sí/í. left. nothing about us without us. me/cfs.Bridget O'Shea
@Bridget_OShea
Certified medical #writer, enthusiastic #journalist, cat mom, @UChicagoProEd, ME/CFS patient. Freelance journalist. Available for medical writing and editing.Kirsty Schnickelfritz
@KSchnickelfritz
Licensed to rest. Untapped resource, just mucking around. #Antirecoveryactivist Pigeon obsessor. Knitting addict.elle W
@elleW902
Nature lover🌊⛰wx watcher🌪️❄️ Ally🌈 ♍️creative🖌#LongCovid Sept 2021 #Dysautonomia #LCPOTS #LCHashimotos KINDNESS is the #1 attribute in a human❤All of them snollygosters...
@OnlyEnnui
@onlyennui.bsky.social Ex philosopher. #MEcfs activist #hEDS. spinal injury, prescribed benzo withdrawal = hell Expect swearing & sarcasmMargherita
@margheritaandME
Two-time cancer survivor (Hodgkin lymphoma) now living with #ME, #PoTS and #hEDS since 2016, mostly house/bedbound. Wife, mother of 2 (8 and 10), dog owner 🐶MoleyMECaroline🦔
@tweetingmole
feel like a mole living in a dark ME/CFS hole sharing thoughts ,trying to make a small difference. Lancs U.K. - #bekind also @MoleyME.bsky.social𝐏𝐚𝐮𝐥𝐚🌷
@flower_of_June
Someday I will write poems about this. But first I must survive it.🪽 Lora Mathis ♡ ☾ ✧ ❀ ✧ ☽ LYME & CO'S | MCAS | ME/CFS | FM | and more🥀Charlotte
@CharlotteClarkW
Blogger | Family History | ME Advocate #pwME #Fibromyalgia #breastcancer Mostly housebound. Lover of old things. Auntie to a multitude. List maker.My Year In A Crash
@myyearcrash
6 year sufferer of ME/CFS. Writing a light-hearted weekly blog on how I coped in the midst of a crash. https://t.co/C2VgEDDWz5 #ME #CF #ChronicFatigueMelissa Mazur
@PhillyPhile215
Just a Philly girl, livin' in a lonely world…and a Luddite learning to Twitter. #LongCovid since March 2020 || Lawyer on PauseCinnamon rolling along
@LongCovidFight
Prev LongCovid Fighter. Not much fight left. Supporting pw chronic illnesses, esp #LC #LongCovidKids #MECFS #PoTS #MCAS. #COVIDisNotOver #COVIDisAirborneAngela Reiersen, MD, MPE
@AngelaReiersen
Associate Professor of Psychiatry @WUSTL ; Opinions are my own; Tweets are not medical advice. Say my name: https://t.co/4CbvdgvJC8G R A C E 🌸
@withgrace___
🥀 severe ME/CFS mama to baby son ❤️ heart full, body broken 🌻 INFJKeanu Reeves
@KeanuReeve624
actor. Born in Beirut and raised in Toronto, he made his acting debut in the Canadian television series Hangin' In (1984), before making my feature film 🎥Chronicillnesswarrior1 ♿️💙✝️💟
@fionangreg
Wife, mum, pwSME/CFS, FND, Fibromyalgia Observe small things, don't rush, love & forgive ❤️ #chronicillnesswarrior #loveyourself #loveotherssharon askew
@88888888881
a tired human
@saffronandsky
disability justice💜 mod. chronic illness for decades+long covid in '22 =severe MCAS, ME+POTs= bedbound. Parent, mixed race, writer, former gardener ♿ 🏳️🌈☸️Lily
@LhousemusicR
ME you moved into my life uninvited,and now you won’t leave. #drowning but not waving, Virtual traveller,Film fan ,house music. Occasionally opinionated.🤯#pwMEFran Haddock
@franhaddock_
Spoonie 🥄 Activist ✊ Vet 🩺 (she/her) Currently bedbound with severe ME + Long Covid (more active on IG)#NotJustFatigue
@njfatigue
We are a 501(c)(3) sounding the alarm on ME/CFS through digestible, creative content. This is #NotJustFatigueA 😎 Long Covid + MECFS Billboards
@AaronCa11
@lcmebillboards https://t.co/0rnAQeYP77Mary Wagner
@MaryWagner31921
Nina A Tomei, MD
@doctormom63
Life derailed #Sjogrens #MECFS #POTS #LongVax Child with #LongCovid Surviving Not Living. Sick Not Tired. Tweets not medical advice. We just want our lives back🌻Kirsty
@Kirstycfsmelife
CFS/ME 15+ years and POTS 🐼 trying to improve my health and one day fully recoverFrancy Aguilera
@Frank717173
Larry Weis
@LarryWeis7
#ME/CFS,#SFN,#Dysautonomia Owner-Commercial Insurance AgencyBrad
@AutonomicBrad
Bachelor of Biological Science Degree. #LongCovid #TeamAutoantibodies #Bc007. Any tweet is my opinion and not medical advice. Check out my podcast on SpotifySharon Cohen
@SharonC97936831
#TwitterHaiku; Tulane MBA; LSE; Univ of Wisc Mad; former career financial services; international bus. #chronicillness; #physicaldisability.. 4 NIH studiesMevin nat stevens
@MevinNat47271
SEALs Dad/ American CitizenRamy2.0
@Ramyisback
I am back from the twitter grave, with memes, and other stuff about mecfs and long covid.Elizabeth Ansell
@elizansell
Founder @njfatigue. Previously at Showtime and ABC News, among other places. Quit career due to #MECFS. This is #NotJustFatigue.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!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.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 ✡️ 🇲🇽🏳️⚧️KK
@KSannara
#ME #MECFS #LongCovid #BildungAberSicher #Petition #MECFS. ➡️https://t.co/EuFUEYyf9j ⬅️Chronically Surviving
@Chronically2784
Queer & Disabled. ME, POTS, Ulcerative Colitis. (she/her)Naomi Beresford
@NaomiBatt002
Lawyer. 5th grade teacher from Texas who loves kids! 🍎 I love traveling & sports. Books and common sense.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.socialGaia Tempest 🦄🦼 🛌
@GaiaTempestUK
Mostly as horizontal as achalasia allows. #ActuallyAutistic, M.E more than 40 yrs. Now more degenerative autoimmune 🙄Trying not to let it all make me 😮💨...Lovro Muani
@LovroMuani54894
Julia
@VanilleSuess
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.AnitaTexasSunshine
@TexasSunshine18
searching medical scientific articles #MS #MECFS 38 yrs #neuroimmune 🧬#HHV6 #EBV #lowNK #blockallbots🧪👒🐴🌵🌞🌎🍀💚💐 🏔️ 🌊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!!erica
@sadfoxqueen
25 💜 chronic lyme and autistic girly ☀️ still masking 🖤 miss gonna be alright somedaycarlos perez
@thecarlos020
𝕟𝕒𝕥𝕦𝕣𝕖 | 𝕙𝕒𝕡𝕡𝕚𝕟𝕖𝕤 | ➸ ᴛʀᴀᴠᴇʟ🌍 Orthopedic Surgeon Doctor. Coffee Loverme_ots
@te_rztoo
ME/CFS (chronic fatigue-syndrome) since 2018/19. We need basic + therapeutic research ! #PEMJane Pike 🇺🇦💙💛
@Janebfc
❤ BFC. 💚 growing food/flowers. Has ME, osteoarthritis, fibromyalgia etc. Recovering political geek. Bit opinionated but *trying* to do it kindly ❤ Ig @janebfcbethereificould
@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 #missingmillionsMD Yashin Khan
@kh78962
Well done Appreciate a person who stays by your side in both happiness and sadness and believes in you. Another thing is that whoever wants to stay like this wiDebbie
@mistydeb_1
Love reading and creating when I can. Life with ME is challenging.Pekka Puupää 🇺🇦
@Raichu_pokem0n
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