Read the Latest in ME News and Campaigns
Never miss a beat! Subscribe to our newsletter and select “Daily Digest” to get a summary of the day’s news & actions delivered to your inbox.
A Bay area-based photographer is seeking people with myalgic encephalomyelitis (ME) who are willing to share their stories and to be
Originally published on ME Australia. by Sam* Sam (*not her real name) is a teenager living in Australia’s largest
By Christopher Armstrong, PhD, OMF Science Liaison When the Harvard ME/CFS Collaborative at Harvard Affiliated Hospitals was initiated last
We’re so excited to announce we’re growing our community’s impact through the expansion of #MEAction USA’s formal State Chapters.
Volunteers are at the heart of everything #MEAction Scotland does. We are always looking for more people to help
I’m Hannah Bowlus and I’m the administrative assistant at #MEAction. I take care of basic things like mailing
On June 3rd the CDC held its latest MECFS Stakeholder Engagement and Communication (SEC) Webinar/Conference Call with the ME
#MEAction has announced two CDC-related advocacy actions today and yesterday. We are asking you to contact your Senators to
Jack Croxall is an author, scriptwriter and blogger living in Nottinghamshire, UK. He fights ME both in life and
Listen to the article: #MEAction co-founder, Jennifer Brea, wrote this letter to the community about her remission of
The story so far NINDS, the National Institute for Neurological Disorder and Stroke at the NIH has solicited an RFI,
#MillionsMissing – organised by #MEAction – has been such a successful campaign this year, and we thank everyone in
It has been a big week, with over 100 public and virtual events happening across the world! We are
Erica Verrillo is the president of the American ME and CFS Society, a 501(c)(3) nonprofit. May is the month
Simmaron Research is conducting a one-of-a-kind study to analyze data from ME/CFS patients who respond to treatments like Ampligen®, IVIG, and cidofovir, and we need your help funding this data analysis! Our goal is to publish peer-reviewed data to stimulate treatment trials and inform rigorous trial design ASAP!
***UPDATE: THIS ACTION IS NOW OVER*** Please contact your SENATORS and urge them to co-sponsor a ME/CFS Awareness
Australians with ME/CFS are routinely rejected from the country’s National Disability Insurance Scheme (NDIS), because the Australian government doesn’t consider ME/CFS to be a permanent condition for most living with the illness. Sign this petition to support Aussies with ME/CFS and demand policy change!
Myalgic encephalomyelitis (ME) is a debilitating, chronic disease that steals so much from the person. Parents with ME are
NINDS, the National Institute for Neurological Disorder and Stroke at the NIH has solicited an RFI, or a Request
Join the protest virtually during #MillionsMissing – May 5th to May 12th Use the hashtag: #MillionsMissing Start sharing photos
Senator Jordon Steele-John has announced the Australian Greens’ policy on Myalgic Encephalomyelitis (ME) and Chronic Fatigue Syndrome (CFS), planning to
#MEAction Medical Travel Scholarship Because of the generous donation from a private family foundation, #MEAction has been able
In January 2019, a survey investigating the impact of graded exercise therapy (GET) and cognitive behavioural therapy (CBT) for