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…
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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…
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…
From Body Politic: On October 4th, 2020, Body Politic admin Alison Sbrana spoke with Clinical Rehabilitation Counselor Dr. Julie Hill about her expertise, what advice she has for Covid patients,…
To better understand the reasons why COVID-19 long haulers continue to suffer with persistent symptoms, we are using the You + ME Registry and Biobank to collect data and biological samples from individuals with and without persistent symptoms. We will also compare these data to information from people with myalgic encephalomyelitis (also known as chronic fatigue syndrome or ME/CFS), to characterize similarities and differences between the two groups.
In this webinar, Solve M.E. President & CEO Oved Amitay and Advocacy & Community Relations Director Emily Taylor talk to Howard and Bishof explore how COVID long haulers and the ME/CFS community can join forces for progress in the study, understanding and management of both COVID-19 and ME/CFS.