I try not to leave my CF links on socials too much anymore but if you’re spending $ on Black Friday pls consider donating $5+ to my medical fundraiser, & sharing w your networks. :) I am trying to reach my goal by Jan. Getting close! gofund.me/241e8944
You can also Venmo me @ itssvee. Ty ❤️
27.11.2024 18:55 — 👍 34 🔁 33 💬 1 📌 1
HUGE THANKS 🏆 to everyone who has signed so far!
We're at ✨8300 signatures✨-- can you help get us to 10k?
This petition closes TODAY so please sign and share, not just here but w/your networks!
15.11.2024 17:34 — 👍 70 🔁 44 💬 1 📌 3
Fingers crossed you come down gently and just get to chill with no side effects 🤞🤞
15.11.2024 22:44 — 👍 1 🔁 0 💬 0 📌 0
Woah! Do you feel like non-ME good or drugged good or both?
15.11.2024 22:42 — 👍 1 🔁 0 💬 1 📌 0
I take 15 mg BID, but I can’t actually tell if it does anything 🤡 I’m just afraid that things would be worse without it LOL
15.11.2024 22:31 — 👍 2 🔁 0 💬 1 📌 0
Telehealth is the only way I can see doctors safely these days.
In person appointments trigger post-exertional malaise #PEM and it takes 1-2 months to recover thanks to #MECFS
Please call/contact your members of Congress and ask them to protect telehealth.
15.11.2024 01:58 — 👍 34 🔁 12 💬 3 📌 1
Very severe Myalgic Encephalomyelitis (ME/CFS) + POTS + hEDS. I can’t reply/interact consistently.
heather 🍂
saskatoon
single sick&disabled (me/cfs) trans lesbian
30
- - -
people from the discover feed pay me $5 before following or get blocked: https://paypal.me/gaaaaay
i am sometimes too sick to post alt text
Struggling with #MECFS, #celiac, #migraine
Former Financial/Data Analyst and College Economics Lecturer.
https://christinalawrence.me
genetics BS ➡️ history MA ➡️ PharmD candidate | 🌈🏳️⚧️ | MECFS | 🇨🇦➡️🇺🇸 | any/all
Aberdeen fan. Passionate about an independent Scotland. SNP member. Live by the sea and a Loch. ME for 11 years #pwME #rejoin #FBPE 🏴
Visual Artist and Writer #ME #pwME #LongCOVID #ZeroCOVID #Crip #ChronicIllness #DisabilityJustice #ContemporaryArt #ConcretePoetry #VisualPoetry #PostdigitalPoetry #PoeticWeb
http://www.diktgymnasiet.com
22 yo w/ ME, PoTS, MCAS & ASD
wheelchair user
covid cautious
previously severe, now moderate-severe
she/he, genderfluid lesbian
http://lifeasbeck.wordpress.com
@Remissionbiome n=50 Participant🍳🧠 🏳️🌈 🏳️⚧️. Disabled by SARS2, Marxist, jew-ish. rts ≠ endorsement $ app and venmo: hiimjakekthx
eighteen and vry tired
#AALD fan account
Writer. Fmr Artist Manager, Publicist. Disability, Chronic & Invisible Illness Advocate. ME/CFS & comorbidities. Intersectional Feminist. She/Her. Living on Gadigal land, Sydney, Australia.
Former academic, social scientist, and mom/caretaker to two kids, including one with long COVID since 2022
Lover of old films, books, Doris Day and Rosemarys Baby and other who-haa. Cranky empath. Dealing with servere ME. and cancer. Politically sensible, sensitive and left.
SevereME/vax injured. Can't read, write, watch, walk or talk much. Just me, my bed & my swollen brain. Trying to stay sane. Roy Kent is my spirit animal.
Co-founder #ThereForME | Calling for an NHS that’s there for ME & Long Covid | www.thereforme.uk
Independent researcher & policy analyst | Migration & displacement | Projects with @odi-global.bsky.social | www.linkedin.com/in/karen-hargrave
Small but mighty, early educator teaching through the early pandemic years. 30 years teaching at-risk children & home visiting families. No longer essential now #LongCovid and #ME. Speak truth to power. #MaskUp 😷#EduSky #EarlyChildhoodEducation #VERMONT
Salty | #LongCovid,#POTS & #ME | Books, Music, Food, Art #ATXRE | Excuse my typos
We are living in a choose-your-own dystopian novel
https://amandafrancey.com/ Australian illustrator, graphic designer, photographer. Advocating for myalgic encephalomyelitis #MECFS #LongCovid #ClimateAction
#PwME, pianist, poet, wanna-be painter
