Keeping ME/CFS in the Fight on Capitol Hill
Hi friends, It’s Monique here, Advocacy Director at Solve M.E., with a progress update on
September 11, 2025
Hi friends, It’s Monique here, Advocacy Director at Solve M.E., with a progress update on
Earlier this year, our partners at the Irish ME/CFS Association for Information, Support and Research
Today, Solve joined #MEAction, Bateman Horne Center, Simmaron Research, Open Medicine Foundation, and other organizations
IACFS/ME’s 17th Conference will take place online October 22-25, 2025, and will focus on the
Because of your persistence, advocacy, and shared determination, Congress is finally starting to listen. This
Dr. Maureen Hanson, a professor of molecular biology and genetics at Cornell University and member
From the ME/CFS Patient, Advocate, Clinical and Research Community Dear Dr. Unger, On the occasion
Dr. Zack Shan is director of the neuroimaging program at the University of the Sunshine
Solve M.E., in partnership with The Brain Inflammation Collaborative (BIC), is excited to announce the
After the pandemic eased (and people practiced less social distancing and masking) came a huge
Dr. Lorna Thorpe, a professor of population health at the New York University School of
The Severe Myalgic Encephalomyelitis (ME) Day of Understanding and Remembrance was started in 2013 by
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