From The Lancet: Published July 15, 2021 Authors: Hannah E. Davis, Gina S. Assaf, Lisa McCorkell, Hannah Wei, Ryan J. Low, Yochai Re’em, Signe Redfield, Jared P. Austin, and Athena…
From The You + ME Registry and Biobank: Emerging evidence has made it clear that, for some, COVID-19 recovery isn’t like flipping an off switch. Thousands of people are still…
Dr. Klimas is an expert on multi-symptom disorders, myalgic encephalomyelitis (ME), Gulf War Illness, fibromyalgia, and other neuro-immune disorders. In the seminar, Dr. Klimas touches on the medical sexism that…
From Solve ME: Solve M.E. recently opened the 2021 Ramsay Grant Program Request for Applications (RFA), which offers competitive funding for studies into myalgic encephalomyelitis (also known as chronic fatigue…
In this first webinar in a series presented by the Long COVID Alliance, learn about the latest research exploring the relationship between POTS and other forms of dysautonomia in post-acute sequelae…
This is a running list of recruiting studies, clinical trials, and research opportunities. If you have an opportunity to add to this list, please contact us. NIH RECOVER Studies RECOVER…
From the Pulmonary Wellness Foundation: In September 2020, Pulmonary Wellness hosted a conversation with Dr. Svetlana Blitshteyn, Director and Founder of Dysautonomia Clinic. The Pulmonary Wellness Foundation has Launched a…
From PhysiosforME: The PhysiosforME team are joined by Professor Todd Davenport and Suzan Jackson to discuss the theory and practice of HR monitoring. For more information please go to: www.physiosforme.com.
From PhysiosforME: PhysiosforME and Dr. Charles Shepherd discuss PVF, PVFS and ME. Personal experiences of supporting people with PVFS and ME, how to distinguish between PVF, PVFS and ME, exercise…
From Dysautonomia International: Dysautonomia researchers from Stanford University and Stony Brook University discuss dysautonomia symptoms that are occurring in some COVID-19 patients, and what COVID patients need to know about…