#MEAction: Fall advocacy round-up - a season of protest and petition An extensive summary of this autumn's advocacy work around the world. Quite...
Here's a relatively easy advocacy action for patients in the USA: Ask your health care professional to watch Unrest online and get continuing...
I am delighted to announce a new ME project, Dialogues for a neglected illness, which Josh Biggs and myself, Natalie Boulton, will be working on,...
Hi, I apologise if this is the wrong area to post this but this is our last formal statement as a family. I’m unsure how to get it to come up on...
We have a bunch of facts we use both for advocacy and for scientific research that we cite often. I spend a good amount of time at #MEAction...
Halp. Looking for a resource on this? I'll start the hunt through Phoenix Rising, but if someone has it handy, I'd really appreciate it.
I thought I would open a thread on this as I'm aware of a number of people who have been nominated. Also votes numbered in the hundreds seem to...
Great video interview "From Fit Nurse To ME Warrior With Ashanti Daniel" by Valentine Ewudo:...
https://www.sciencedirect.com/science/article/pii/S1369848617300705 The Biopolitics of CFS/ME Author Nikos Karfakis Highlights •The diagnosis...
/Movement Action Plan/, by Bill Moyer. http://www.indybay.org/uploads/movement_action_plan.pdf excerpt: === STAGE TWO: PROVE THE FAILURE OF...
Finally, the old feminist slogan that the personal is political holds true, but it also works the other way around. The political has to be...
#ME Action Network have just announced a fundraiser for a U.K. organiser. “to support another year of mass awareness, medical and scientific...
Invest in ME Research has been contacted by a researcher on a Sky One programme called What’s Up TV – an arts and culture magazine show with a...
Sign the MEAction letter to Francis Collins to increase investment in ME research (Global) Ask Congress to support people with ME. Using our...
Note: This isn't intended as a partisan post, vote for who you want, I just see potential for ME advocacy in it. Send us your questions for...
Australians with ME/CFS continue to be harmed by GET. If you’ve been harmed by GET, write a letter to one of our campaign targets (RACGP...
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I'm a big believer in the cliche that gets beaten into every writing workshop student: show, don't tell. I'd rather someone show me that he or she...
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...
Facebook question: How can I create an ad targeted at people interested in myalgic encephalomyelitis or Chronic fatigue syndrome? I was previously...
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