https://www.meaction.net/2019/08/01/meaction-responds-to-attacks-on-me-community-in-the-guardian-and-psychology-today/?mc_cid=0039916b6f&mc_eid=ee6...
A new project from ME Action: #MEAction is excited to announce the launch of our Postcards to Doctors medical education campaign. Send...
From their Facebook post We are excited to announce that as of today we are rebranding as ME Advocacy Network Australia, affectionately known as...
Up with the Marines! We are so pleased that Congressman Jack Bergman (R, MI-1), a former Marine general, has become a champion for people with...
We are thrilled to announce the release of our 2019 research summary reviewing the most current and important research into myalgic...
Hi, I have everything ready for the Sunday Millions Missing event except one item. I want to create a poster to put up near our table. I ended...
My husband and I are planning a small #MillionsMissing event at our local library in Beaverton, Oregon. We plan to set up a small table in front...
It has been been an exciting time for the myalgic encephalomyelitis (ME) community these past few weeks. We are in awe of the sacrifices and hard...
Not a particularly bad article that quotes #MEAction a lot (The Myalgic Encephalomyelitis Action Network). However, I question the bit at the end...
A little late but still worth posting I think. Because of the generous donation from a private family foundation, #MEAction has been able to...
Most of us are not able to go to Washington, DC for this advocacy week. But there are still ways to make your voices heard! Today I called both...
https://www.meaction.net/2019/03/25/a-response-to-dr-mark-porters-article-about-me-in-the-times/ Last week, Dr. Mark Porter wrote an article in...
Last week was a difficult time for the ME community as we watched a few journalists deride and dismiss the medical concerns of an entire patient...
The U.S. National Academy of Medicine (NAM) is holding a contest for young people (ages 5 to 26) to submit art, music, writing, videos, dance,...
Earlier this month, NIH director Francis Collins and other agency officials held a meeting with five representatives from #MEAction. According to...
This Christmas, millions will be missing from parties and celebrations, because of the severity of ME. Yet the National Institute of Health and...
From an #MEAction email: A few months ago, #MEAction Executive Director Jennifer Brea released an open letter, outlining the importance of...
Congress to HHS: What's replacing CFSAC? ME/CFS must be represented! On September 6, the Secretary of Health and Human Services disbanded the...
I got an alert via email a couple days ago requesting folks in the USA to contact their congressional representatives. Signature deadline has...
A few things have begun to aggregate, so I figured I would start a new thread and post them here. First, #MEAction's general article on how to...
Separate names with a comma.
