Action Alert: Another appropriations effort that directly impacts ME/CFS
A quick note to loop you in on another appropriations effort we’re in support of – one that directly impacts our ME/CFS community, with a deadline tonight! Senators Markey (D-MA), […]
Solve M.E.’s Appropriations Efforts for 2024
At Solve M.E., our mission is to drive research and advocacy efforts for Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS), Long Covid, and other infection-associated chronic conditions and illnesses (IACCIs). This year, […]
Solve M.E. Announces Emily Taylor as New President and CEO and Publication of New White Paper Calling for NIH to Restructure Funding for ME/CFS, Long Covid, and other IACCIs
Solve M.E. is pleased to announce that Emily Taylor, Vice President of Advocacy and Engagement, has been appointed as President and CEO. Emily has been a key member of Solve’s […]
Solve Spearheads Call for New NIH Office for Infection-Associated Chronic Illness Research (IACIR)
This year, Solve is beginning one of our most ambitious advocacy projects to date — one which could alter the research landscape for ME/CFS, Long Covid, and other infection-associated chronic […]
Solve CEO Oved Amitay joins the NIH ME/CFS Research Roadmap Working Group
In 2019, the National Institutes of Health (NIH) National Advisory Neurological Disorders and Stroke (NANDS) Council Working Group for ME/CFS presented the Report of the NANDS Council Working Group for […]
Solve M.E. Advises and Reacts to Administration Reports on Long Covid
In April, President Biden issued a Presidential Memorandum directing the Secretary of Health and Human Services (HHS) to coordinate a new effort across the federal government to develop and issue […]
Solve M.E. Calls For Congressional Action After Budget Delays Thwart ME/CFS Research Centers
The National Institutes of Health (NIH) recently published a long-expected request for applications (RFA) for the Collaborative Research Centers (CRCs) for ME/CFS, announcing that the funding levels for the centers […]
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 […]
You helped secure $1.15 billion for research!
This is our biggest victory, yet! Earlier this month, Solve M.E. led the charge for federally funded research into Long-COVID and myalgic encephalomyelitis (ME) — previously known as chronic fatigue […]
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 […]
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 […]
