This is the third in a series of blogs following the work of Workwell and allied exercise physiologists who are aiming to do nothing less than revolutionize the way chronic fatigue syndrome / myalgic encephalomyelitis (ME/CFS) is viewed. The Disability Defenders:...
Given the ubiquity of herpesviruses, the common infectious trigger in ME/CFS and the fact that once you’re infected with them – you’re infected for life – it’s no surprise that researchers have been interested in herpesviruses and ME/CFS...
It was a typically warm July southern Florida day as we pulled out of our hotel to find one exit blocked by construction. Google Maps sent us in another direction, and when that didn’t work out, we made our own map and, once again, hurried with time running out...
“New data collectively supports the presence of specific critical points in the muscle that are affected by free radicals.” Fulle et. al. A group of pioneering Italian researchers have been studying the muscles of people with ME/CFS – a rather...
The Solve ME/CFS Initiative’s Ramsay Awards are small grants (@$50K – only in the medical field is 50K small) but potentially mighty grants. They are designed to give researchers the funding to produce pilot data needed to get really big grants – the...
Thanks again to Veronique for providing her intriguing take on chronic fatigue syndrome (ME/CFS). This is one of a series of articles from Health Rising which feature hypotheses created by health care professionals with ME/CFS or who are associated with ME/CFS. (It is...
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