Watch now! “Opportunities for Action: Infection- Associated Chronic Conditions”
The Infection-Associated Chronic Conditions Patient Advocacy Coalition (IACCPAC) hosted a national webinar on October 24th, 2023, led by The Long Covid Alliance, Solve M.E., COVID-19 Longhauler Advocacy Project, Dysautonomia International, […]
Join Solve’s Long Covid Research and Advocacy Patient Training Program
We’re thrilled to share that Solve M.E. has been awarded a grant from the Chan Zuckerberg Initiative to support our Long Covid Patient Leader Advancement Network (LC-PLAN). LC-PLAN is […]
Long Covid Alliance, Solve M.E. Secure $77k CDC Foundation Grant to Form New Patient Advocacy Coalition
Today, Long COVID Alliance proudly announced it will begin establishing a new Infection Associated Chronic Conditions Patient Advocacy Coalition (IACC PAC) using $77,000 in grant funding through the CDC Foundation’s […]
Watch Now! The Effects of Long Covid and ME/CFS on Sleep
Many individuals who have had COVID-19 experience long-term symptoms that have a major impact on their lives. One of the most common symptoms is sleep disturbance. After more than six […]
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 […]
US ME/CFS Clinician Coalition Publishes Consensus Letter Asking Doctors to Consider ME/CFS in Differential Diagnosis of Long Covid
The US ME/CFS Clinician Coalition has published a consensus letter asking doctors to consider ME/CFS in the differential diagnosis of Long Covid, especially when post-exertional malaise (PEM) is present. Early […]
Solve-funded Grantee Strengthens Connection Between ME/CFS and Long Covid Exercise Intolerance
Solve M.E. funded Dr. David M. Systrom at Brigham and Women’s Hospital in 2017 to study exercise intolerance in ME/CFS. Six years later, his findings have redefined our understanding of […]
Solve Honors Dr. Peter Rowe
As Advocacy Week in Washington, DC drew to a close last week, Solve M.E. honored Dr. Peter Rowe for his work as a medical provider, researcher, educator, and advocate for […]
US Government Seeks Public Input on the Definition of Long Covid
A National Academies of Sciences, Engineering, and Medicine (NASEM) committee will conduct a series of public workshops to examine the current U.S. Government (USG) working definition for Long Covid and […]
Solve Brings Army of Advocates to Capitol Hill, Presses Congress to Support the Care for Long Covid Act
Advocacy Week 2023 unites Long Covid, ME/CFS communities in an effort to educate congressional representatives, marking the first in-person gathering for the event since 2019. LOS ANGELES, CA – Today […]
CDC Publishes Findings from Multi-Site Clinical Assessment of ME/CFS (MCAM) Study
In 2012, the Centers for Disease Control and Prevention (CDC) initiated its multi-site clinical assessment of ME/CFS (MCAM) study, enrolling and following ME/CFS patients recruited from multiple specialized clinics in […]
NIH Awards $9.5M Grant to Study ME/CFS
The Cornell Center for Enervating Neuroimmune Disease has received a five-year grant of nearly $10 million from the National Institutes of Health’s National Institute of Allergy and Infectious Disease, enriching […]
