History made! Department of Defense Funds Its First-Ever ME/CFS Research Projects
Since 2017, unleashing the potential research funds from the Department of Defense (DOD) for ME/CFS has been one of our highest priorities. After more than three years of hard work, […]
You + ME Registry Reaches New Milestone: 2,000 Registrations
We’re thrilled to announce that enrollment in the You + ME Registry has reached 2,000 participants! This would not have been possible without the support of this amazing community. Together, […]
November is National Family Caregivers Month
November is National Family Caregivers Month, offering an opportunity to acknowledge the vital contributions made by family caregivers everywhere. In the ME/CFS community, we know the difference a loving caregiver […]
Honoring People with ME/CFS for Invisible Disabilities Week
As we strive to make myalgic encephalomyelitis, otherwise known as chronic fatigue syndrome, or ME/CFS, more diagnosable and treatable, we are always aware that many people suffer with this disease […]
Journal of the American Medical Association (JAMA) article brings awareness to Long Covid and Solve M.E. Registry as a tool for research
A recent article about COVID-19 “long haulers” in the peer-reviewed medical journal The Journal of the American Medical Association (JAMA) referenced Solve M.E. and our You + ME Registry and […]
Watch our H.R. 7057 Town Hall Meeting
Watch now: The H.R. 7057 Legislative Cafe Chat Hosted by Emily Taylor Earlier this year, Representative Jaime Raskin introduced H.R. 7057, the Understanding COVID–19 Subsets and ME/CFS Act. This landmark […]
Solve M.E. Hosts H.R. 7057 Legislative Cafe Chat
Join Solve M.E. for an H.R. 7057 Legislative Cafe Chat on Sept. 9! We’ve received dozens of emails from you asking questions about the historic legislation endorsed by Solve M.E. […]
Your Advocacy In Action Part 1: ME/CFS Senate Resolution Introduced
Your ME/CFS Advocacy Week actions continue to make a difference! Senator Ed Markey, a longtime champion for people with ME/CFS and people with disabilities, introduced S. Res 633, Supporting the […]
Watch Now! The Congressional Roundtable on Women’s Chronic Illness During a Pandemic
Watch now! The Congressional Roundtable on Women’s Chronic Illness During a Pandemic Last week, as part of our collaboration with the Congressional Bipartisan Women’s Caucus, Miles for Migraine, and the […]
ME/CFS and COVID-19 Long-Haulers: Read Our Op-Ed in The Guardian
Solve M.E. Chief Executive Officer Oved Amitay and Solve M.E. Research Advisory Council Member Dr. Anthony L. Komaroff (Professor of Medicine at Harvard Medical School and Senior Physician at Brigham […]
The Solve M.E. Spring 2020 Chronicle is available online now!
The electronic version of our flagship research and advocacy journal, The Chronicle, has arrived! It answers the question “Could Improved Testing for Orthostatic Intolerance Lead to Better Care?” and includes a look […]
Together, We’re Sponsoring an Historic ME/CFS Legislation!
Four Years of Advocacy has paid off! We’re Proud to have Authored and Initiated the First Ever Legislation for ME/CFS Research Funding, H.R. 7057, The Understanding COVID-19 Subsets and ME/CFS Act […]
