Researching “the greatest medical scandal of the 21st century”. Infection-Associated Chronic Illness, activism, stigma, medical humanities. Postdoctoral fellow in Sociology.
Freelance science & medical journalist | Bylines in Nature, C&EN, Veritasium, ScienceAlert, The Guardian, ABC News, news.com, Croakey, The Medical Republic | http://frogsandstars.com (she/her)
A UK registered charity for people with #MECFS and Long Covid (and Post Covid ME/CFS). We inform, educate, raise awareness, fund medical research and campaign for positive change.
RPs do not necessarily mean endorsement.
https://linktr.ee/meassociation
Co-founder #ThereForME | Calling for an NHS that's there for Long Covid & ME | https://www.thereforme.uk/
Linguist, DELTA-qualified English 2nd lang teacher | https://hiveofactivities.wordpress.com
Design | https://emmarubystudio.com/
She / her
🇦🇺 South Australia
🏳️🌈 Queer
👩⚕️ Retired doctor - ME/CFS & POTS advocate (Doctors with M.E. associate + Australian POTS foundation member)
🌏 Climate crisis advocate (Climate and Health Alliance member + Doctors for the Environment Australia member)
To improve the lives of all people affected by ME/CFS, Fibromyalgia, Long COVID, and other Infection-Associated Chronic
Conditions and Illnesses (IACCIs) through advancing awareness, care, treatment and research.
https://www.massmecfs.org
anthropologist working on biomedicine/debility/capital. she/her dog dad 🇵🇸
emilylimrogers.com
Long COVID and HIV cure clinician and researcher
I play language. Mostly irreverent. Debugger.
AI. Global warming. Integrity. Health. Science.
Chronically ill punk rocker.
I think about the future a lot.
Severe ME patient currently on a 10% battery, the gas goes out more than I do. I also compile ME/CFS Awareness videos.
https://linktr.ee/abrokenbattery
The Bateman Horne Center is a medical center of excellence for people with ME/CFS, Long COVID, fibromyalgia, post-viral illness, and comorbid conditions.
Artist/teacher with me/cfs, adhd, cats and a vegan kitchen 😷
Living on Whadjuk Noongar Boodja.
https://www.lucindacrimson.com
Not-for-Profit Organisation supporting Australians living with ME/CFS (mylagic encephalomyelitis / chronic fatigue syndrome) and long COVID.
Education | Research | Advocacy | Support Services
Website: www.emerge.org.au
Donate: www.emerge.org.au/donate/
Actress on Pause with Myalgic Encephalomyelitis
🌍 Florence, Italy <-> Melbourne, Australia
🎙️ Writer, Producer, Actor
🦋Living that Stockdale Paradox life
Collaborative #research center based at Cornell directed by Dr. Maureen Hanson encompassing a variety of projects on #MECFS. Visit our website below for more info.
Researching the cell biology of ME/CFS since 2016, now also Long COVID and PD. Papers: https://scholars.latrobe.edu.au/d2missailidi/publications
Phonetics PhD. Life on hiatus with ME/CFS. Cats, music and excessive screen time. Naarm/Melbourne. (she/her)
Providing support & holistic healthcare services to people of all ages affected by #MECFS
Charity number: 1036419 / SC040452
