Government Shutdown Disruptions and Community Support
As of this week, the federal government has shut down, and the impacts are already
October 2, 2025
As of this week, the federal government has shut down, and the impacts are already
Hi friends, It’s Monique here, Advocacy Director at Solve M.E., with a progress update on
Today, Solve joined #MEAction, Bateman Horne Center, Simmaron Research, Open Medicine Foundation, and other organizations
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