Solve M.E., Long COVID Alliance highlighted in U.S. News & World Report

In her U.S. News & World Report article, “In Long COVID, Advocates Battling Chronic Fatigue Syndrome See Allies, Hope,” journalist Chelsea Cirruzzo examines the ME/CFS and Long COVID connection, and how the striking similarities are fueling hopes that research can uncover solutions for both. Mentioned in the piece are Solve M.E. President Oved Amitay and the Long COVID […]

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Postdoctoral Fellowship to Foster Trans-Atlantic ME/CFS Research Collaboration

Solve ME partners with Action for ME on two-year research fellowship focused on identifying molecular drivers of ME/CFS May 2021–Solve M.E. and Action for ME are excited to share that Dr. Chris Ponting and Dr. Liz Worthey will work with postdoctoral fellows as part of the Solve/Action for ME trans-Atlantic partnership. This two-year, jointly funded, […]

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Ramsay Grant Program 2021 RFA is Open!

  Solve M.E. will accept applications to study ME/CFS and Long Covid from February 22 – April 30, 2021 Through the Ramsay Program, Solve M.E. invests in research studies in ME/CFS or Long Covid with a particular emphasis on engaging young investigators and researchers new to the field. Collaborative proposals (involving 2 or more research […]

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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 Edinburgh on the world’s biggest biomedical study of the causes of ME/CFS! The DecodeME genome-wide association study will enroll 20,000 individuals with ME/CFS living in […]

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Register for Our December Webinar! “You + ME: A Registry for the Whole ME/CFS Community”

After months of collaborative development with community members and researchers, we opened the You + ME Registry for enrollment in June 2020. You + ME is driven by a big vision — building a community of thousands contributing health information to create the largest dataset ever for ME/CFS research. Many research projects have come to […]

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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 last few weeks, I’ve received dozens of emails from you asking questions about the historic legislation we’ve endorsed. We are thrilled with the engagement you’ve demonstrated […]

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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 Goals of International Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) Awareness Day Thanks to the combined efforts of Solve M.E. and the Massachusetts ME/CFS & FM Association, […]

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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 at the new YOU + M.E. Registry and its part in Bringing the Big Data Revolution to ME/CFS. You’ll also get to meet the new Solve M.E. Community Advisory […]

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You Can Make a Difference in the Lives of People with M.E.

We Can’t Thank You Enough for Your Meaningful and Generous Support We know and deeply appreciate your passion for our mission. It’s caring people like you who make our battle against ME/CFS possible. We haven’t stopped fighting for you during the Coronavirus (COVID-19) pandemic. Our staff may all be working from home during the quarantine, […]

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