CDC Update: Recent Strides in Long Covid

In this webinar, Solve M.E. President Oved Amitay welcomes Dr. Elizabeth Unger, chief of Chronic Viral Diseases Branch at Centers for Disease Control and Prevention, and her CDC colleagues to share updates […]
Solve M.E. & Community Partners Denounce Misleading New York Magazine Article

The article published in NY Magazine on Nov 4, 2022, “Has Long COVID Always Existed? The pandemic might not have spawned a new chronic illness but rebranded an old one,” […]
Long Covid & Fatiguing Illness Recovery Program

Research Update Featuring: Avindra Nath, MD (Clinical Director of National Institute of Neurological Disorders and Stroke – NIH; Chief of the Section of Infections of the Nervous System – NIH; […]
Pediatric Post-COVID Conditions

Long COVID & Fatiguing Illness Recovery Program Presenters include: Peter C. Rowe, MD Director of the Chronic Fatigue Center at Johns Hopkins Children’s Center Professor of Pediatrics at Johns Hopkins […]
Tracking of ME/CFS Cases in the Revised US ICD-10-CM

Since 2015, the 1-2.5 million Americans with myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) have been effectively nonexistent, at least as far as US disease tracking systems are concerned. Americans don’t experience […]
Solve M.E. Joins Lawmakers in Asking CDC to Make Long Covid Data Publicly Available

Dear friend, This week, Representatives Ayanna Pressley and Don Beyer authored a letter to Centers of Disease Control and Prevention (CDC) Director Dr. Rochelle Walenksy asking the CDC to make […]
CDC ME/CFS Stakeholder Engagement & Communication Conference Call
The Centers for Disease Control (CDC) holds regular Stakeholder Engagement and Communication (SEC) calls to update the ME/CFS community on CDC activities and facilitate presentations from guest speakers. The next […]
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, […]
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 […]
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 […]
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 […]
Victory! Six Major Federal Wins for ME/CFS

Dear Friends, Throughout 2019, I reported on our advocacy gains for ME/CFS. Thank you for standing with me and our advocacy partners during a particularly turbulent year while we fought […]