History made! Department of Defense Funds Its First-Ever ME/CFS Research Projects
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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!
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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!
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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 […]