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

we will win. "I would very much like to be excluded from this narrative." civis civitatis novi eboraci. dum spiro spero.

Empowering persons w Myalgic Encephalomyelitis. 35y w/ME Colab at ONG PEM Spain, ME-International.org, EMEA ICPrimer our best tool. #UniteToFight2024 Empoder

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

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

Grief support & writing workshops to help you heal ancestral relationships, connect with nature, and to put your best story forward. #AuDHD #spoonie 🏳️‍🌈🏳️‍

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.