…online, made sure to have some non-ME/CFS excursions and adventures, and conducted a successful crowdfunding campaign so I can continue this project for another year. (That campaign will continue through…
…they chose to exclude them from the series. They attended a symposium at Stanford University on the molecular basis of ME/CFS, which included prominent researchers from around the world, including…
…in children with chronic fatigue syndrome, otherwise known as myalgic encephalomyelitis, CFS/ME or ME/CFS. As I have noted, the study has provided Lightning Process practitioners with an opportunity to cite…
…October, so I can’t even go to the event and ask him a few pertinent questions about his treatment of people with ME/CFS, or whichever name people choose to use…
…and employ people with ME, which Action For ME piloted at Bristol’s NHS CFS/ME specialist service in 2015-2016. Here’s what the tool-kit states: The information and advice presented in this…
…review of the matter. I have not yet heard back from you. Since my academic position at UC Berkeley’s Center for Global Public Health involves investigating ME/CFS research and related…
