Watch! Protecting the Ones You Love: Legal & Insurance Tools for ME/CFS Caregivers
Caring for someone with ME/CFS is an act of deep love–and preparation is one of
February 12, 2026
Caring for someone with ME/CFS is an act of deep love–and preparation is one of
Solve M.E. is proud to share that our President and CEO, Emily Taylor, has authored
About HB27: This bill would establish a state-level grant and loan initiative through TEDCO to
Dear Friends, As this year comes to a close, I find myself thinking not just
This year, you made the difference. In a year filled with gridlock for biomedical research
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
Thank you to Patient Advocate & Researcher Deborah Duricka, PhD, for the below toolkit. Full
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
