Retired maths teacher. ME/CFS 35 years. Volunteer staff member on Science for ME international forum, www.s4me.info

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

settler-descended grandmother activist-scholar whose work examines intersection of climate, water, food, and colonization #Grantifa She/they #LandBack #FoodComm

Informed decisions & verifiable facts please, not opinion & belief. UK. 🇬🇧 Mine of occasionally useful information. NHS and healthcare 💙 #Equality #Justbe #I

I occasionally try to explain and comment on ME research, or even contribute to it. And I advocate for more and better research.

I play language. Mostly irreverent. Debugger. AI. Global warming. Integrity. Health. Science. Chronically ill punk rocker. We must know. We will know.

42-jährige Münchnerin mit #MEcfs nach einer Corona-Infektion im April 2022, die Hörbücher 📚, Podcasts 🎙️ und die #kleineKunstklasse 🎨 mag.

Politics, local economies, social investment, credit unions, financial Inclusion, money for good. If you haven’t posted anything, I won't follow you. Cats, Ir

Sweetness n’Lightenment, anti-invisibility potions, and fog horns to find lost spoons. Got mostly A's: Activist Anti-fascist Ace Agender Animist Arab-American

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.