From the The Massachusetts ME/CFS & FM Association: Since 1985 we have offered support to patients and their caregivers for ME, CFS and FM. We now offer support to those…
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…
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…
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. 2. Email this to your…
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…
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.
This article by Robert Glatter, MD was originally published by Forbes on February 20, 2021. As people with long Covid come to grips with ongoing symptoms such as fatigue, chest pain, difficulty…
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…