Senate Appropriations: Big Wins for ME/CFS — Thanks to Your Advocacy
Because of your persistence, advocacy, and shared determination, Congress is finally starting to listen. This
August 25, 2025
Because of your persistence, advocacy, and shared determination, Congress is finally starting to listen. This
From the ME/CFS Patient, Advocate, Clinical and Research Community Dear Dr. Unger, On the occasion
The Severe Myalgic Encephalomyelitis (ME) Day of Understanding and Remembrance was started in 2013 by
It’s official! The state of Alaska will officially recognize May 12 as ME Awareness Day.
We’re excited to share the newest edition of our flagship journal, The Chronicle! Inside, you’ll
From June 23–27, over 200 fierce, compassionate advocates came together from all across the country
One of the cornerstones of our annual Advocacy Week program is the EmPOWER M.E. roundtable.
The Congressionally Directed Medical Research Program (CDMRP) is a lifeline for service members, veterans, and
Congress slashed over 57% of funding from the Congressionally Directed Medical Research Programs (CDMRP), which
Myalgic encephalomyelitis (ME), also known as chronic fatigue syndrome (CFS), is a debilitating illness that
The federal government is considering eliminating the CDC’s only program dedicated to Myalgic Encephalomyelitis/Chronic Fatigue Syndrome
Tell Congress to Restore Our Research! Reverse the 57% Cut to the Congressionally Directed Medical
