Environmentalist. Scientist. Love to travel. Born and bred in Sheffield.
Migrated to bluer friendlier skies.
#MECFS
Life is being autistic and chronically ill with ME and writing about it. Doodle artist. Smorky's human. Scotland. She/her.
https://linktr.ee/phoebsbo
Trying to be a good human. Living with Myalgic Encephalomyelitis.
Learning as I go, but aren't we all. San Diego, CA. Living with illness and doodling for fun. #LongCovid, Severe #MECFS, hyper #POTS, #FM, hEhlers Danlos, Idiopathic Subglottic Stenosis ( #ISGS ), …
👋ME/CFS ,Fibromyalgia , lyme Boriliose,Longcovid,MCS ,Vax Injured (not corrona vax),Hearing loss ect… Posts English and German.
Bavaria ,Germany
I run marathons around Europe raising funds for Invest In ME's biomedical research projects to cure ME.
34 countries so far. £52k raised.
Next race: #39 Sarajevo, Bosnia (26.04.26)
www.mikeseumarathons.eu
www.justgiving.com/mikeseumarathons
Professor of Communication and Psychology at BI Norwegian Business School and the University of Oslo
Past Yale, Harvard, UiB. Editor-in-Chief at Advances.in
Father. Views are my own.
Guardian columnist and journalist. Commentator of the Year 2024. Author of Who Wants Normal? and Crippled.
E: frances.ryan.freelance@guardian.co.uk
Victoria, Australia. Former professional wordsmith. 15+ years living with the hell of myalgic encephalomyelitis (ME/CFS). Prone to so-called left-wing views & bingeing good TV 🤓
Here to talk about #MEcfs, #MEspine, #hypermobility, #POTS, #hEDS, #LongCovid, #ChronicIllness and #disability ...but I also have opinions on other things. You have been warned :P
One of the #MillionsMissing with #LongCovid #MECFS JohnVsJon.com // Once a radio and podcast producer, always a Transom alum
😷 Long covid is common 😷
Interested in research and awareness of invisible chronic illnesses: ME, Long COVID, Post Vaccine injury, POTS, Sjogrens, and Lyme.
Pfp: A man wearing a green face mask
Banner: Colorful MEmes from patient-led Long COVID and ME awareness
Ella/she/her. I write, I read, I draw plants. Chronically ill en la Ciudad de México. #ME #MECFS #POTS #LongCovid
Cat and Dog botherer. Young persons counsellor retired. Want my bike and my health back 🩵
Person with #LongCovid for 5 and a half years.
Disability Campaigner and dog lover. Left-wing. Member of The Green Party
Hates Centrists for pandering to the Right.
Leveson 2 Now. Anti-Zionist. Anti-Racist pro-Trans
• Scientist ‖ PhD mathematical physics (not MD) ‖ Dr. rer. nat.
• Interests: Medicine ‖ History ‖ Global Politics
• #MECFS ➡️ http://mecfs.de/was-ist-me
• EN ‖ PL ‖ DE
I'll "tweet" here about the things I don't like if the other app goes down
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/videos/
London, UK
No DMs please
#pwME
ME since 2017 (Mild), 2019 Moderate , 2020 Severe
Long Covid since March 2020 (V Severe)
Funcap55 = 1.9 ( (Severe)
ME/CFS (1993) | Long Covid (2020).
Occasionally Support @ Visible Health
