Solve M.E. Calls For Congressional Action After Budget Delays Thwart ME/CFS Research Centers
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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 […]
Registration now open for Solve M.E. 2021 Advocacy Day!
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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, […]
NIH launches database to track neurological symptoms associated with COVID-19
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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
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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!
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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
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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 […]
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. Advocacy Director Emily Taylor Answers All Your Questions About H.R. 7057 in this Q&A and Town Hall!
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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 […]
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 […]
Senate Advocacy Action: $60m for ME/CFS Research
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Tell Your Senator to SUPPORT INCREASED FUNDING FOR POST-VIRAL-DISEASE RESEARCH INTO ME/CFS! Thanks to your hard work during ME/CFS Advocacy Week, the U.S. Senate is currently circulating our request to include […]
Meet the new members of the Solve M.E. Community Advisory Council
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2020-2022 Community Advisory Council Announced Solve M.E. is pleased to announce the inaugural 2020-2022 class of the Community Advisory Council (CAC). Due to overwhelming response to the call for nominations, […]
Advocacy Success! Florida Members of Congress Take Action for ME/CFS
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Florida Members of Congress Take Action for ME/CFS Solve M.E. teamed up with local Florida advocates to launch a lightning advocacy action with huge success this week. Congressmen Gus Bilirakis […]