Living with Myalgic Encephalomyelitis and Postural Orthostatic Tachycardi Syndrome, so no longer working. Married, and have two grown up daughters.

Depleted human. Slowly making photographs about a life with ME/CFS, like Long Covid. https://linktr.ee/andrewgifford.photography Bristol, UK. 335.42 ppm. He/h

Severe ME/CFS with added Long Covid. Running a support group in Cambridge, UK. Pronouns: depends how the day pans out

Graphic & web designer, mainly using this account for illness fieldnotes. ♿ Chronically ill & disabled with ME/CFS, MCAS, hEDS, Psoriasis, Endometriosis/Adenom

Biomedical engineer, mathematician, equestrian, thru-hiker and generally outdoorsy - now 99% bedbound with #severeME. I like posts on science, literature, world

Disabled advocate - #Interiordesigner - #Anthropology student - Multi local - #SWYer - #Fibro + #MECFS - 1 of the #MillionsMissing + #Disabledguerrera https://

I believe we are ALL better off when EVERYONE has housing, healthcare, food, and education. If you're fond of punching down - especially when it comes to blami

23 | #MECFS #SFN | hausgebunden

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

ME/CFS Warrior not by choice but destiny (Profilbild: sick not tired in Schönschrift, große Fahne: moderate ME, darunter ein Haus, vor dem ein Rollstuhl steht,

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.