A Quick Guide to Advocacy Week 2026
Solve M.E. and #MEAction are joining forces for a week of coordinated action designed to move ME/CFS from optional knowledge to the standard of care in clinical training — and […]
Join the Fight for Federal Research Funding and Medical Education for ME/CFS
Appropriations season is moving fast this year, and we are proud to share that Solve M.E. has submitted our FY27 appropriations letters to both the House and Senate Labor-HHS and […]
Welcoming Jessica Maya, PhD, Solve M.E.’s New Vice President of Scientific Programs
Solve M.E. is proud to welcome Dr. Jessica Maya as our new Vice President of Scientific Programs, a role central to how we advance discovery, collaboration, and impact across the […]
Advocacy Update: Three Crucial ME/CFS Federal Budget Wins
Hi all, I wanted to circle back with a quick update: the federal funding bills covering Labor, Health and Human Services and the Department of Defense are now final. This […]
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 the budget process. We’re right in the thick of appropriations season — when Congress decides […]
Senate Appropriations: Big Wins for ME/CFS — Thanks to Your Advocacy
Because of your persistence, advocacy, and shared determination, Congress is finally starting to listen. This year’s Senate Appropriations bills include some of the strongest support for Myalgic Encephalomyelitis/Chronic Fatigue Syndrome […]
A Thank You to Dr. Beth Unger from the ME/CFS Community
From the ME/CFS Patient, Advocate, Clinical and Research Community Dear Dr. Unger, On the occasion of your retirement from the Centers for Disease Control and Prevention, we – patients, caregivers, […]
Solve M.E.’s Appropriations Efforts for 2024
At Solve M.E., our mission is to drive research and advocacy efforts for Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS), Long Covid, and other infection-associated chronic conditions and illnesses (IACCIs). This year, […]
CDC Publishes Findings from Multi-Site Clinical Assessment of ME/CFS (MCAM) Study
In 2012, the Centers for Disease Control and Prevention (CDC) initiated its multi-site clinical assessment of ME/CFS (MCAM) study, enrolling and following ME/CFS patients recruited from multiple specialized clinics in […]
CDC Responds to Solve M.E. Comments on Draft Review of Diagnosis and Treatment of ME/CFS
In 2018, the Centers for Disease Control and Prevention (CDC) announced it was soliciting bids to create evidence-based treatment guidelines for myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS). In 2019, the CDC […]
CDC Update: Recent Strides in Long Covid
In this webinar, Solve M.E. President Oved Amitay welcomes Dr. Elizabeth Unger, chief of Chronic Viral Diseases Branch at Centers for Disease Control and Prevention, and her CDC colleagues to share updates […]
Long Covid & Fatiguing Illness Recovery Program
Research Update Featuring: Avindra Nath, MD (Clinical Director of National Institute of Neurological Disorders and Stroke – NIH; Chief of the Section of Infections of the Nervous System – NIH; […]