Join the National Health Institutes (NIH) RECOVER Research Review (R3) Seminar Series, "Leveraging EHR/Real World Data to Understand PASC," by registering here: http://ow.ly/sZep50Jg45C. The goal of the R3 Seminar Series is to catalyze a shared understanding of the research of the scientific stakeholder community within the RECOVER Consortium. Working and learning together while keeping each other up […]
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 our panel of veteran state advocates as they discuss the importance of local and state advocacy. We’ll hear about initiatives in CA, FL, MA, MD, […]
The Global Interdependence Center – Solve Long Covid Initiative Program Series: Session III: Long Covid and Children. The Global Interdependence Center, in partnership with the Solve Long Covid Initiative, is conducting a year-long webinar and conference series exploring the pandemic’s long-term healthcare, policy, and economic impact, specifically the implications of Long Covid. This program will feature speakers […]
The Patient Perspective on Post-Infectious Fatiguing Illnesses Sonak Pastakia, PharmD, MPH, PhD, BCPS, FCCP ME Patient since 2017 Professor of Pharmacy Practice Purdue University for Health Equity and Innovation A CDC-funded monthly webinar-style ECHO learning session to rapidly disseminate Post-acute Sequelae of COVID-19 (PASC) and Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) findings and emerging best practices. […]
Join the Institute for Neuro-Immune Medicine (Nova Southeastern University) on Friday, June 10th for their annual 2022 INIM Conference. The Institute's clinicians and researchers will discuss research and the various clinical approaches to ME/CFS and Long Covid. Patients, caregivers, family members and friends are welcome to attend. Register here.
In 2019, Francisco Westermeier, PhD, was awarded a Ramsay Research Grant by Solve M.E. to study endothelial function in ME/CFS. Like many other researchers in the Ramsay network, Dr. Westermeier has since been dedicated to expanding the ME/CFS knowledge base. In the coming months, Dr. Westermeier and his team will be working to expand evidence […]
Dr. Jarred Younger’s 2016 Ramsay Award was used to show that brain temperature is elevated in ME/CFS. This increased temperature is a sign of brain inflammation. The findings are now being replicated in a large group of individuals with ME/CFS. Dr. Younger’s lab is now developing new magnetic resonance imaging (MRI) and positron emission tomography […]
Many patients with ME/CFS experience common herpesviruses infections at their disease onset. Alternatively, others experience reactivation of the same infections during the disease course. These facts suggest the existence of a disease-specific antibody signature related to these viruses. However, current evidence is conflicting about this signature due to the heterogeneous nature of the disease, the […]
In this special webinar, Dr. Steven Deeks (Professor of Medicine-in-Residence at the University of California, San Francisco) will be hosted by Solve M.E. Medical Advisor Dr. David Hardy (former Director of Division of Infectious Diseases at Cedars-Sinai Medical Center, Los Angeles, and Professor of Medicine at David Geffen School of Medicine, University of California, Los […]
Join a special presentation by Solve M.E.'s Emily Taylor during the 2022 Virtual Scientific Conference from July 27 - 30, 2022! Meeting events include workshops, Keynote lecture by famed immunologist Akiko Iwasaki, PhD (Yale University, USA), Plenary Lecture by innovative ME/CFS clinician-researcher David Systrom, MD (Harvard Medical School, USA), and oral/ poster presentations of original […]
Join Solve M.E.'s research team at this year's IACFS/ME for a special presentation by Solve M.E.'s Kate Mudie, as well as a poster session, during the 2022 Virtual Scientific Conference from July 27 - 30, 2022! Presentation: Do people with joint hypermobility represent a subgroup of myalgic encephalomyelitis/ chronic fatigue syndrome? Poster Session: Baseline Characteristics […]
Each year on August 8, Severe ME/CFS Awareness Day, we reflect on the tremendous toll this devastating disease takes on individuals suffering from severe ME/CFS symptoms and remember the lives of those we have lost. People living with severe ME/CFS are often bed-bound and unable to perform everyday tasks without assistance — eating, showering, and […]
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