Severely Ill ME / CFS and Family’s Struggle Featured in a Mini-Documentary
Our own ME / CFS Scientific Advisory Board director, Ron Davis, PhD, and his family, struggle with severe ME / CFS. Whitney, Dr. Davis’ son, has it. This has
Our own ME / CFS Scientific Advisory Board director, Ron Davis, PhD, and his family, struggle with severe ME / CFS. Whitney, Dr. Davis’ son, has it. This has
As word is spreading about the ME / CFS Severely Ill-Big Data Study, the first study of the End ME / CFS Project, organizations and bloggers are revealing more
The NIH released its P2P (Pathways to Prevention) report with suggestions on what types of ME / CFS studies should be conducted. As most expected, the panel
Linda Tannenbaum, our organization director, explains our new study: the ME / CFS Severely Ill, Big Data Study. Geoff Langhorn hosted her in May, 2015, on his
After a careful review of what is needed to “End ME / CFS,” our ME / CFS Scientific Advisory Board determined the first step is to look for answers
By Linda Tannenbaum A February Institute of Medicine report said up to 91 percent of people with chronic fatigue syndrome have not been diagnosed. These people are
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