omg thank you! it’s actually an original by yours truly! i used to be a painter. haven’t been able to in quite awhile, which is a shame. but i plan on setting up a studio space in my apt soon and doing just a little at a time. i really miss it.
19.11.2024 13:02 — 👍 0 🔁 0 💬 0 📌 0
ps i did put on pants before i left
14.11.2024 16:04 — 👍 3 🔁 0 💬 0 📌 0
i’m always amazed at how i pull myself together right before i go to the doctor. anyway hello everyone i have arrived 🦋 #severeME #dysautonomia #POTS
14.11.2024 16:03 — 👍 8 🔁 0 💬 2 📌 0
They/them | 28 | ME/CFS since 2016, very/severe since 2022 after covid | Severe hyperacusis
Mostly post about ME but will share things relating to disability justice, leftist & queer issues and Palestine 🇵🇸
In "Australia" on Wurundjeri Country
🇨🇦
www.lizwhitmere.com
Signal: @lizw.85
I dress up in fancy dress for the charity Invest in ME Research to raise funds & awareness of Myalgic Encephalomyelitis. In a previous life I worked in film. I’m an advocate for good science, treatments & better healthcare for #pwME.
Former Skier, Cyclist, Climber, Hill Walker, Diagnostic Radiographer and functioning human. Now - ME, POTS, LC, Vax Injury - Pro Vax - Still finding the joy
Installation artist. Perfume fanatic. Chronically ill. Concordia University PhD student(disability studies + performance studies + practice-based research.) Ex jammer, current failure. She/her Montréaler in Edmonton. https://linktr.ee/ChloeLum
Ella/she/her. I write, I read, I draw plants. Chronically ill en la Ciudad de México. #ME #MECFS #POTS #LongCovid
Serving genderqueer drag and goth looks
Brit living in California
Genderqueer Drag as https://www.instagram.com/lordofmxrule
Painted rocks https://www.instagram.com/stained_stones
thinker, poet, cinephile | chronically ill | advocate | polyglot … she/they
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
exposed late january 2020, fucked up since march 2020
National nonprofit led by people with lived experience helping families navigate pediatric Long COVID with support, resources, and advocacy.
OMF is fundraising to support open, collaborative research to find effective treatments and a cure for ME/CFS, Long COVID, and related diseases.
Author, illustrator, comics creator
THE FACTS OF LIFE (Myriad) Kidlit Books x3
Writing illustration comics poetry photography
https://linktr.ee/paulajknight
https://www.redbubble.com/people/PaulaJKnight
https://ko-fi.com/bedscapepaula
Bedridden pwME ♿
Dutch | life derailed due to #IBD & #MECFS | sofa bound | wants to raise awareness about post infectious diseases | one of the #MillionsMissing
P/w Long Covid, writer, nerd, ENM, loudmouth, green thumb, artist, queer, ND, & unstoppable!
No alt text= no RT
#FBLC #LongCovidAid
Scientific Director, #MEAction
Stanford Med
Université de Montréal
TIME100 Health 2024
#ME, #EDS, #POTS, #LongCOVID
Views my own
exceedhergrasp1 on Twitter
Wife, mum, Severe ME, 💙✝️♿️Fibromyalgia
Observe small things, don't rush, love & forgive
#loveyourself #loveothers ❤️
#chronicillnesswarrior1 on X & IG
Opinions are my own 🤓
One of the #millionsmissing || Raising awareness of the most severe form of #MyalgicEncephalomyelitis
ME/CFS since 2019, painter, yoga and health enthusiast. The healthiest sick person I know and on a quest for turning this around!
PhD in physics, former scientist, educator, and athlete, now housebound due to ME/CFS and POTS from SarsCov2, she/her
