Patient advocate by choice: Solve M.E.’s Oved Amitay
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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!
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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 […]