New York Times Cites Solve M.E Whitepaper, Quotes VP of Advocacy Emily Taylor
This week, New York Times writer Peter Coy’s piece, “Pushing ‘Long Covid’ Sufferers Too Hard Could Cause Them to Crash,” cited our recently released whitepaper, Long Covid’s impact on adult […]
Ask Congress to TREAT & CARE for Post-Infection Diseases During Advocacy Month
Advocacy Month is an opportunity to share the policy solutions vital to address the growing number of individuals suffering from ME/CFS and Long Covid. ME/CFS devastated the lives of an […]
ME/CFS: NO problem?
Nitric oxide (NO) – a gas produced by cells lining the blood vessels (endothelial cells) – helps to promote the widening of blood vessels (vasodilation) and is involved in the […]
Solve M.E. Calls For Congressional Action After Budget Delays Thwart ME/CFS Research Centers
The National Institutes of Health (NIH) recently published a long-expected request for applications (RFA) for the Collaborative Research Centers (CRCs) for ME/CFS, announcing that the funding levels for the centers […]
World ME Day
Solve M.E. is proud to be a partner in the first-ever World ME Day, May 12, 2022. We’re joining ME/CFS organizations around the world to campaign together and raise awareness […]
EmPOWER M.E.: State Advocacy
This year, our EmPOWER ME roundtable will focus on local advocacy. They say “all politics is local.” What does that mean for creating change for ME/CFS and Long Covid? Join […]
Solve M.E./UCLA Announce Pilot Funding for ME/CFS Research
Second year of Solve/UCLA partnership September 2021–Solve M.E. is again partnering with the University of California, Los Angeles (UCLA) Iris Cantor Women’s Health Center to fund ME/CFS research through their Annual Health […]
ME/CFS Symptom Checklist
Myalgic encephalomyelitis, also referred to as chronic fatigue syndrome (ME/CFS) is a complex and chronic disease that can have a serious impact on one’s quality of life. Patients can experience […]
Advocacy Director Emily Taylor On Sharing the Success of ME/CFS Advocacy Week
During Solve M.E.’s ME/CFS Advocacy Day 2018, 102 people with myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) and their loved ones joined us in the largest Capitol Hill action for the disease […]
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 […]
Finding Resources and Creating Opportunity: 2020 ME/CFS Federal Advocacy Report
After an eight-month politically-charged rollercoaster, Congress ended 2020 by passing a $900 billion COVID-relief package and a $1.4 trillion FY21 budget simultaneously. This giant bill, totaling over 5,500 pages, was […]
You helped secure $1.15 billion for research!
This is our biggest victory, yet! Earlier this month, Solve M.E. led the charge for federally funded research into Long-COVID and myalgic encephalomyelitis (ME) — previously known as chronic fatigue […]
