Replicable Results in ME/CFS? Yes, Finally.
It’s a turning point researchers wait years, even decades, for: results that replicate. In our
December 9, 2025
It’s a turning point researchers wait years, even decades, for: results that replicate. In our
As part of our ongoing coalition work, Solve M.E. joined over 157 organizations in urging
November is National Family Caregivers Month. It is a time to recognize and honor the
As of this week, the federal government has shut down, and the impacts are already
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
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
Dr. Candace Feldman is a rheumatologist and assistant professor of medicine at Harvard University. She
It’s official! The state of Alaska will officially recognize May 12 as ME Awareness Day.
From June 23–27, over 200 fierce, compassionate advocates came together from all across the country
Congress slashed over 57% of funding from the Congressionally Directed Medical Research Programs (CDMRP), which