Australia:
International Awareness Day for Chronic Immunological and Neurological Diseases (CIND) including myalgic encephalomyelitis (ME) / chronic fatigue syndrome (CFS)
Sandgate Town Hall will be lit up Blue for International Awareness Day for Chronic Immunological and Neurological Diseases...
Learn About the Millions Missing from ME/CFS – Sundance Award-Winning Film Screening and Panel Discussion
January 15, 2019 5:30 PM - 7:00 PM
Boston
https://www.massbio.org/events/learn-about-the-millions-missing-from-me-cfs-sundance-award-winning-film-screening-and-panel-discussion-3244...
I would be very grateful for suggestions for the most useful articles from big international newspapers (or similar sources) in giving background info on Unrest, Brea and the expanding global MillionsMissing events May 12th.
Any you would recommend?
I really like this article from The...
Hey, everyone, can I ask anyone who still has some energy to help out?
#MEAction is collecting press coverage about #MillionsMissing. Especially the local stuff is important.
It would involve finding link, author, news outlet, country, and putting that into a Google spreadsheet. I just did...
Bustle:
"You may have noticed the hashtag #MillionsMissing trending on social media, or may have seen some landmarks lighting up blue over the past few days. That's because May 12 is International Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) Awareness Day, and the folks posting in...
This is part one of my interview with The Canary about my song and the #MillionsMissing campaign. Part two will be published tomorrow: https://www.thecanary.co/feature/2018/05/12/bob-dylans-blowin-in-the-wind-has-been-re-imagined-for-the-millions-missing-part-one/
Edit: And here is part two...
Thought it would be good to have a thread to help people follow what's happening today, worldwide.
If you go here and click 'Latest' (just below the blue #MillionsMissing bar), there's tons of tweets:
https://twitter.com/search?q=#millionsmissing&lang=en
Anybody got links to video coverage...
Perhaps this article demonstrates the value of @dave30th 's recent awareness-raising trip in Australia.
To the #MillionsMissing with ME/CFS, something remarkable is happening...
The Body - The Complete HIV/AIDS Resource
Journalist Olivia G. Ford
Using Lessons From HIV Activism, People With Chronic Fatigue Syndrome Fight for the #MillionsMissing
Simpson and Wilder both use the skills they've gleaned over decades as HIV activists to understand who has the power to make...
LIVE ACTION SATURDAY!
Prime Minister Trudeau Apologizes to Canadians with ME.
Okay, not quite yet -but wouldn't that be great?
Prime Minister Justin Trudeau needs to see Canadians with ME on Millions Missing Day on May 12th if we want to move meaningfully toward equitable health care and...
Hi folks,
I just got off a planning call with ME Action volunteers about how to coordinate #MillionsMissing events planned for May 12th.
I was encouraged to register an event with ME Action. I learned that even though all I am going to do for May 12th this year is take some photos and share...
The segment starts at 2 hours 11 minutes with a brief description of the symptoms of ME.
A chat with Philip Murray, @phil_in_bristol,
one of the organisers of this year's #millionsmissing in Bristol. He describes how he became ill 20 years ago, and how it took six months before he could stand...
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