You + ME has joined the world’s biggest study of ME/CFS
We are excited to announce we’re partnering with our UK colleagues Action for ME and Professor Chris Ponting of the Medical Research Council Human Genetics Unit at the University of […]
Solve M.E. Joins 57 Other Organizations In a Call to Action for Health Equity
Solve M.E. joins with the National Health Council (NHC), the National Minority Quality Forum (NMQF) and our partners in patient advocacy to end structural racism in the healthcare system and […]
Chronic Disease Stakeholders Join Solve M.E. in Push for Federally Funded Research into Long COVID
December 4, 2020 Jointly authored letter serves as a warning about the increasing number of COVID-19 patients experiencing post-viral complications. LOS ANGELES, CA — Twenty leading chronic disease stakeholders joined the […]
ME/CFS Federal Funding: What We Know So Far
Thank you for your patience and for standing with Solve M.E. and our advocacy partners during a particularly turbulent year. Despite unprecedented obstacles, we accomplished victories and produced dollars for […]
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 […]
43 Bipartisan Co-Sponsors Pledge Support for ME/CFS Bill!
Rep. Jamie Raskin’s landmark legislation, H.R. 7057, The Understanding COVID-19 and ME/CFS Subsets Act, will be the first piece of legislation to authorize funding from the National Institutes of Health […]
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. […]
Solve M.E. Advocacy Director Emily Taylor Answers All Your Questions About H.R. 7057 in this Q&A and Town Hall!
Hi Solve M.E. Community! In case we haven’t met before, my name is Emily Taylor, and I’m the Director of Advocacy and Community Relations at Solve M.E. Over the […]
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 […]
