Patient advocate by choice: Solve M.E.’s Oved Amitay
This article by Charlotte Kilpatrick originally appeared on VaccineNation.org. Although the World Vaccine Congress West Coast is a few months away, we and our speakers are already gearing up and preparing a […]
Solve Appropriations Efforts Are Going Strong!
Last month, we shared big appropriations wins for our ME/CFS and Long Covid community members via the FY24 Department of Defense Appropriations Report from the House of Representatives, which included […]
Big Appropriations Wins for MECFS & Long Covid
Congressionally Directed Medical Research Programs (CDMRP) provide funding to support therapeutic research related to medical threats, and treatments for service members in current and future battlefield settings. In recent years, […]
The Future of Symptom Tracking: Exploring STAT Health’s Revolutionary In-Ear Device That Measures Blood Flow to Head
Solve M.E. is excited to host STAT Health CEO Daniel Lee for a conversation about their innovative in-ear wearable device. We’ll discuss how the STAT in-ear wearable measures blood flow […]
World ME Day raises awareness of devastating symptom impacting millions post-COVID
To mark World ME Day on May 12, 2023, the World ME Alliance and its 22 member organizations are proud to announce the launch of a global awareness campaign addressing […]
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 […]
IACFS/ME 2023 International Scientific Conference
Mark your calendars July 27 – 29, 2023 for the IACFS/ME’s International Scientific Conference to be held at Stony Brook University in Stony Brook, New York, USA. This will be their […]
The Institute for Neuro Immune Medicine: ME/CFS Conference
The Institute for Neuro Immune Medicine will host the conference in the Alan B. Levan Innovation Center on the Nova Southeastern University campus in Davie, FL May 19th 12:30 – 5pm […]
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 […]
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 […]
Using a Heart Rate Monitor to Prevent Post-Exertional Malaise in ME/CFS & Long Covid
This article was first published on ProHealth.com and is reprinted on SolveME.org with permission of ProHealth and the author Suzan Jackson. Though originally written for individuals with ME/CFS managing PEM, members […]
EmPOWER M.E. 2023: Navigating the World with Energy Limiting Disabilities
Hosting EmPOWER M.E. during Advocacy Week each year is one of our favorite ways to connect with our community after a long week of congressional meetings. This year, our Lived […]
