People who have chronic Lyme disease are a mystery in the same way that people with ME/CFS who come down with an infection and never recover are. A recent study that asked why chronic Lyme patients don’t recover could have implications for ME/CFS. It also asked...
Kunisha Miwa has published no less than five studies on the small heart findings in ME/CFS. Now he moves onto a related puzzle – why the blood volume in ME/CFS is low? Health Rising takes a look at his present study, combines his findings with some others, and...
A Very Exciting Presentation Two years ago, Marcie and Mark Zinn produced what I thought were the two most exciting presentations of a very exciting Stanford Symposium. They had used a technology called qLoretta to analyze EEG findings in a way that hadn’t...
Nobody in the chronic fatigue syndrome (ME/CFS) community had taken leptin – a hormone produced by fat cells – seriously, until Jarred Younger’s Stanford Good Day Bad Day study suggested that it might be the factor driving fatigue n ME/CFS. Younger...
Fibromyalgia/ME/CFS sure feels like it’s in the muscles. After exercise, at least for me, they’ll often feel constricted and painful and muscle stiffness is common. The central “sensitizationists: (look -a new word :)) say those pain sensations are ...
Dr. Montoya’s Stanford ME/CFS Initiative opened in 2009 with a $5 million donation. Seven years later it’s published just two studies. Is the Initiative in trouble or is it on the brink of success? Find out more in Will 2016 Finally be Montoya’s...
A BIG thanks to everyone whose contributions helped make Health Rising's summer drive a success :)
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