CDMRP Program at Department of Defense Announces $1.6M Grant for ME/CFS Research
At Solve M.E., our advocacy team is dedicated to opening new funding avenues for ME/CFS, Long Covid, and post-infection disease research and care. We’re excited to share that our efforts […]
Solve M.E. Welcomes Ilise Friedman, Major Gifts Officer
Our team at Solve M.E. is excited to announce that Ilise Friedman recently joined us as major gifts officer to provide her over two-decades long development experience and help us […]
Signature Event Summary — Long Covid: Research, Policy and Economic Impact
As part of our efforts via the Solve Long Covid Initiative, we’ve partnered with the Global Interdependence Center on a year-long webinar and conference series exploring the pandemic’s long-term healthcare, […]
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 […]
Long Haul Voices Episode Two Available Worldwide!
The second episode of our three-part video series, Long Haul Voices, is available to view online now! In this episode, we highlight the voices of prominent medical professionals, scientists, and […]
AIM ImmunoTech Announces Update on Ampligen Long Covid Development Program
Today, AIM ImmunoTech, an immuno-pharma company focused on the research and development of therapeutics to treat multiple types of cancers, immune disorders, and viral diseases, including COVID-19, provided an update […]
Solve M.E. Announces Worldwide Launch of Long Haul Voices: Living with Long Covid and ME/CFS in Honor of World ME Day 2022
https://www.youtube.com/watch?v=W_UFlzaNU6g&list=PLbO5abv0daLXDapXhiaVgeDJaIU66DRDA&index=1 New and timely series will amplify the experiences of individuals with Long Covid and myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) to improve care and increase understanding Today, in honor of […]
Honoring May 12: World ME Day
On May 12th each year, we focus a day on learning about, raising awareness of, and campaigning around Myalgic Encephalomyelitis, or Chronic Fatigue Syndrome (ME/CFS). ME/CFS dramatically limits the activities […]
Solve M.E. CEO Oved Amitay and Dr. Leonard Jason Write Letter to the Editor, Nature
DePaul Univeristy Professor of Psychology Leonard Jason, PhD and Solve M.E. President and CEO Oved Amitay recently co-authored a response to a Nature article linking Epstein-Barr virus (EBV) and multiple […]
Solve M.E Kicks Off Advocacy Month Highlighting Long Covid’s Widespread Impact, Spotlight on ME/CFS
Advocacy Month 2022 focuses on connecting people with ME/CFS, Long Covid, and other related illnesses—brings together scientists, clinicians, and caregivers to educate Congress and the world As the prevalence and […]
CDMRP for ME/CFS: Navigating the Grant Application Process
Solve M.E. hosted special guest, Cecilia Dupecher, PhD Program Manager for PRMRP at the Congressionally Directed Medical Research Programs (CDMRP) for an informational webinar designed to better inform and prepare […]
Trial By Error: Two Reports on the Financial Burden of Long Covid and Its Impact on ME/CFS Prevalence
This piece was originally published in Virology Blog by David Tuller, DrPH on April 20, 2022 and is republished here with permission. It is clear that long Covid—however that term […]
