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 […]
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 […]
Solve M.E. Research Team at IACFS/ME 2022 Conference
Join Solve M.E.’s research team at this year’s IACFS/ME for a special presentation by Solve M.E.’s Kate Mudie, as well as a poster session, during the 2022 Virtual Scientific Conference […]
Is There a Herpesviruses-Related Antibody Signature In Patients With ME/CFS?
Many patients with ME/CFS experience common herpesviruses infections at their disease onset. Alternatively, others experience reactivation of the same infections during the disease course. These facts suggest the existence of […]
New Hope for Diagnosing and Treating Post-Infection Illnesses: Lessons Learned from HIV/AIDS
In this special webinar, Dr. Steven Deeks (Professor of Medicine-in-Residence at the University of California, San Francisco) will be hosted by Solve M.E. Medical Advisor Dr. David Hardy (former Director […]
2022 INIM Conference
Join the Institute for Neuro-Immune Medicine (Nova Southeastern University) on Friday, June 10th for their annual 2022 INIM Conference. The Institute’s clinicians and researchers will discuss research and the various […]
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 […]
How We Can See ME/CFS Inflammation in the Brain
Dr. Jarred Younger’s 2016 Ramsay Award was used to show that brain temperature is elevated in ME/CFS. This increased temperature is a sign of brain inflammation. The findings are now […]
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 […]