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

Unbeliever (political & religious), Wales rugby, #c4news, porridge, tea, #MEcfs 'Obvious but wrong' Also JTJ on the other place https://johnthejack.com

Physiker, Patentingenieur. Blockiere, zB Logikabstinenzler, verdächtige Accounts, InvestierDichReich usw. / (😷+8💉) : 0🦠

Disabled by very Severe Post-COVID ME/CFS. Not always able to use phone. Bedridden. Unable to Speak. I care. Ⓐ💚, (FR/DE/EN, but posts in english) Clinging

She/her Halifax, Nova Scotia Halisky Long Covid Knitting Dogs & cats Urban gardening (zone 6b) Climate change Transit

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

🌱🏳️‍🌈🏳️‍⚧️ ENG: they/them DE: Janne (keine Pronomen)

95% of posts on #MyalgicEncephalomyelitis, #LongCovid or #chronicillness. With ME/CFS 37 years, severe ME 32 years. @IrishMECFSAssoc trustee 29 years 26 publ

I let science form my opinion not the other way around. Views my own; misinfo gets hidden

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