The Long COVID Alliance was recently mentioned in an article by journalist Chelsea Cirruzzo for U.S. News & World Report. Cirruzzo writes, “Guidance on how health care providers can identify…
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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…
Americans who are unable to work due to long-term Covid-19 symptoms could help overhaul the country’s disability system. Read this US News & World Report article, featuring the Long COVID…
by Karyn Bishof I am a COVID-19 Long Hauler and I have been sick for a year. March 15, 2020 was the day I first became symptomatic, with a sore…
One out of three Covid patients, or 8.4 million Americans, have persistent symptoms months after they first got sick, a recent study shows. In post-Covid clinics across the country, doctors…
The You + ME Registry and Biobank is an online clinical study of individuals committed to identifying a cure for ME/CFS, long-COVID and other post-viral illnesses. The community is made…
From the COVID-19 Longhaulers Advocacy Project: Our master document, A Comprehensive Guide for COVID-19 Longhaulers and Physicians, has been revamped and updated. Read it here. Save the link. Updates automatically…
From Body Politic: In light of recent public conversations about the role of exercise, neural training, and cognitive behavioral therapy in Long COVID recoveries, we at Body Politic want to…
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…
Members of the Long COVID Alliance have drafted key recommendations and guidance for the National Institutes of Health, including a list of scientific initiatives from the research community to highlight…