Advocacy Week Kicks Off with Virtual Keynote Address by Rep. Jamie Raskin
Advocacy Week Kickoff Event with Rep. Jamie Raskin (MD-08) The 5th Annual Solve M.E. Advocacy Week will take place from Sunday, April 18, 2021 to Saturday, April 24, 2021. Please […]
Meet Our 2021 Advocacy Week Partners
Advocacy Week Welcomes Partners from Long COVID and Rare Disease Communities The 5th Annual Solve M.E. Advocacy Week will take place from Sunday, April 18, 2021 to Saturday, April 24, […]
Solve M.E. Spearheads Formation of Long COVID Alliance to Accelerate Post-Infectious Research
Today, Solve M.E. warmly welcomes 50 new partners in the fight to return millions of Americans to health. The Long COVID Alliance, launched by Solve M.E., is a network […]
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 […]
Registration now open for Solve M.E. 2021 Advocacy Day!
The 5th Annual ME/CFS Advocacy Day April 20, 2021 The 5th Annual ME/CFS Advocacy Week will take place from Sunday, April 18, 2021 to Saturday, April 24, 2021. This year, […]
Solve M.E. President Oved Amitay joins World Health Organization seminar on Long Covid
Solve M.E. President and CEO Oved Amitay will join other experts as a participant in a series of seminars presented by the World Health Organization (WHO) designed to improve our […]
10 ME/CFS Organizations Join Solve M.E.’s Letter to Congress Recommending Priorities for Federal COVID-19 Relief Package
Last month, Solve M.E. identified yet another COVID-19 relief package funding opportunity for ME/CFS and worked with our friends on Capitol Hill to outline additional federal post-viral research and medical […]
NIH launches database to track neurological symptoms associated with COVID-19
A new database will collect information from clinicians about COVID-19-related neurological symptoms, complications, and outcomes as well as COVID-19 effects on pre-existing neurological conditions. The COVID-19 Neuro Databank/Biobank (NeuroCOVID), which […]
Finding Resources and Creating Opportunity: 2020 ME/CFS Federal Advocacy Report
After an eight-month politically-charged rollercoaster, Congress ended 2020 by passing a $900 billion COVID-relief package and a $1.4 trillion FY21 budget simultaneously. This giant bill, totaling over 5,500 pages, was […]
Memorial fund for son of ME/CFS champion Rep. Jamie Raskin
This week, we learned of the tragic passing of Tommy Raskin. Tommy is survived by his sisters, Hannah and Tabitha, and his parents, Congressman Jamie Raskin and Sarah Bloom […]
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, […]
