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 […]
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 […]
Long COVID & Fatiguing Illness Recovery Program ECHO
History of ME/CFS Lucinda Bateman, MD Medical Director, Provider, & Research expert in the diagnosis and treatment of ME/CFS. Founder and Chief Medical Officer of the Bateman Horne Center of […]
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 […]
In Review: A Year of COVID-19 in the U.S.
This year the one-year anniversary of the first confirmed case of COVID-19 in the United States. It’s difficult to overstate the impact the COVID-19 pandemic has had on the world […]
Chronic Disease Stakeholders Join Solve M.E. in Push for Federally Funded Research into Long COVID
December 4, 2020 Jointly authored letter serves as a warning about the increasing number of COVID-19 patients experiencing post-viral complications. LOS ANGELES, CA — Twenty leading chronic disease stakeholders joined the […]
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 […]
Watch Now! The Congressional Roundtable on Women’s Chronic Illness During a Pandemic
Watch now! The Congressional Roundtable on Women’s Chronic Illness During a Pandemic Last week, as part of our collaboration with the Congressional Bipartisan Women’s Caucus, Miles for Migraine, and the […]
ME/CFS and COVID-19 Long-Haulers: Read Our Op-Ed in The Guardian
Solve M.E. Chief Executive Officer Oved Amitay and Solve M.E. Research Advisory Council Member Dr. Anthony L. Komaroff (Professor of Medicine at Harvard Medical School and Senior Physician at Brigham […]
Senate Advocacy Action: $60m for ME/CFS Research
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 […]
ME/CFS Advocacy Week Continues: Can You Hear M.E. Now?
Can you hear M.E. Now? Call Congress Today! We connected with over 47% of congress yesterday. But we’re not done yet! Today we’re focusing on phone calls to […]
