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…
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From #MEAction: We knew this was coming. So many people with myalgic encephalomyelitis (ME), also known as chronic fatigue syndrome (CFS), develop the disease after an infection, up to 80% in…
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,…
In this podcast, Todd shares with us his research in ME/CFS and post-exertion malaise (PEM). He discusses the characterisation of ME/CFS, the challenges with the word “fatigue” in describing a…
In this webinar hosted by the Massachusetts ME/CFS and FM Association Research Support Club, Roshan Kumar, PhD (Biochemistry) provides information about the COVID vaccines and answers questions from listeners.
In this video, we will be discussing the research, the clinical lab protocol for patients, and the Chronic COVID treatment center. A few moderators from the long haulers advocacy groups…
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.