Infection-associated chronic illness advocate | Life sidelined by #LongCovid #MECFS #POTS | #PatientPartner | MSc | Mom | She/Her | 🇨🇦 #Canada #Quebec #Covi

💙🕯️ Civilians are not targets

Former healthcare worker #MECFS #FM

tired mom. used to teach. long covid since March 2020.

NZ museums and heritage aficionado, shoe fancier, curator baiter, demure chocoholic, and all-round-caffeine fiend. Personal views; Not those of my employer.

ME after covid infection Feb'22. Bedbound. 🛌 #ThereForME #GreatestMEdicalScandal #PEM 🇬🇧🇲🇫🇪🇦🇧🇪

Surviving MyalgicE aka ME/CFS & AAG to tell the story, pwME & advocate w/ a JD. Into MEdical, Social, Climate Justice & Arts. ME-dical apolide, Human Neutrino,

Punny, crafts, chronic illness, math, snow They/Them

Interdisciplinary #Canadian Collaborative #MyalgicEncephalomyelitis Research Network (created in 2019). #MECFS #PwME #LongCovid (Account managed by Sabrina.)

ME-dically gaslit for 10yrs.

Artist, researcher. Anthropology, experimental archaeology, painting, sculpture, visual communication. Slowed but not entirely stopped by ME/CFS. Ottawa, Canad

Speaking up for everyone affected by severe/very severe ME/LongCovidME. #MEKills #MaeveInquest #pwME backstory: https://x.com/swastrosarah?lang=en-GB Justice4M

🇨🇦Project Canary Org - 🇨🇦 NPO - Educator - Researcher - Podcast Host/Producer - Writer - ME/CFS - www.project-canary.org - chronicler - observer- 🥄- ND - s

Living with ME/CFS since 1983. An advocate since my diagnosis in 1988.

95% of posts on #MyalgicEncephalomyelitis, #LongCovid or #chronicillness. With ME/CFS 37 years, severe ME 32 years. @IrishMECFSAssoc trustee 29 years 26 publ

Irish Myalgic Encephalomyelitis/Chronic Fatigue Syndrome Association-for Information, Support & Research NB: Posts ≠ advice. Registered Charity RCN 20100254.