Just a #pwME/CFS, an #unpaidcarer for my wife who has rheumatoid arthritis and for our #SEN son, navigating my way through life and #ElectiveHomeEducation. In a

NSFW Artist in Milwaukee. ULTRA GAY/QUEER, 18+ ONLY. Closeted nudist. Furry! https://www.furaffinity.net/gallery/kingchromanda/

Lever et mikroliv og fascineres av mikrolivet i jorda🌱 #pwme #millionsmissing

Senior Advisor, UC Berkeley Labor Center (retired). All views are my own.

It's me View just my art in the Feeds tab. VVV 18+ NSFW

ME secondary to Covid vaccination. pro vax/vax injured. Zero tolerance for personal abuse. Do unto others as you would have others do unto you.

ME/CFS | Long COVID | IACC

Myalgic Encephalomyelitis - M.E + POTS for 38 years Donor to the UK MEcfs Biobank for 10 years & @DecodeMEstudy Please watch http://dialogues-mecfs.co.uk/vide

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,

Furry/Comic Book/Horror Aficionado/Writer Mature Account, so 18+ only AO3: https://archiveofourown.org/users/Detective_Odin_Ashcroft_52 FA Page: https://www.

Disease genomics & molecular mechanisms; ME/cfs: http://decodeme.org.uk, SequenceME @ Edinburgh University. Views - my own. He/him.

ME-dically gaslit for 10yrs.

Occupational Therapy Lecturer at Australian Catholic University. Returned from UK to Brisbane. Interested in #MECFS #PWME #mentalhealth,#OTeducation

Our world is not pre-given, it's enacted. Physics of biology & cognition; mind & socio-material practices; political ecology. All views, expressed or not, are

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

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

An advocate of social justice for all. Living with ME/CFS/ Long COVID. A lover of science, nature, music, the arts, life, the universe & everything. From Irelan

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