Severe ME patient currently on a 10% battery, the gas goes out more than I do. I also compile ME/CFS Awareness videos. https://linktr.ee/abrokenbattery

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

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,

thinking Web | writing code | making music | fighting long covid If you write stupid code, your code does stupid things. --- 🐘 https://mastodon.social/@floby

Anthropologist in the margin

Climate crisis, reader, me/cfs, allergies. You DM, I block.

Disabled by #MyalgicEncephalomyelitis ° Ambulatory wheelchair user ° Nazi lives don't matter ° Science is real ° #AuDHD ° #Lutruwita I mostly repost things rat

Former professional ballet dancer | Bed/sofa-bound M.E. patient | Using BlueSky to raise awareness for #MyalgicE | #IACC I #PAIS #art2cureME #pwme #millionsmi

Former DJ/Event Manager | Administrator #MEcvs Infokanaal (Youtube) | Advocate for more biomedical research for post-infectious #MEcfs & #LongCovid | 🇧🇪 🇪🇺

Housebound by MECFS, mostly bed/ Sofa since 2022 Bildschirm triggert PEM, deshalb selten hier & Energiebudget reicht nur für liken und weiter verbreiten Lebe in

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.