Solve CEO Emily Taylor Reflects On What We Built Together In 2025 and Why It Mattered
Dear Friends, As this year comes to a close, I find myself thinking not just
December 30, 2025
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
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.