Tag Archives: ME/CFS

[Update from Sept. 2018 here!] This interview with Dr. Willy Eriksen, a research professor at the Norwegian Institute of Public Health, is the second of three blog posts on his hypothesis regarding the cause of and potential cure for myalgic encephalomyelitis, aka chronic fatigue syndrome (ME/CFS). Here I ask Eriksen to elaborate on his published hypothesis. So please see the first post for a summary of his hypothesis in relatively plain language—or, if you have access, read his journal article, “The spread of EBV to ectopic lymphoid aggregates may be the final common pathway in the pathogenesis of ME/CFS.”

In the third post, I consider Eriksen’s model in comparison to other recent research and my own experience. Continue reading →

[Update from Sept. 2018 here!] In a recent paper, Dr. Willy Eriksen proposes a complete explanation for the development, diversity, and persistence of myalgic encephalomyelitis, aka chronic fatigue syndrome (ME/CFS). He also suggests a possible cure. Seeing that this potentially groundbreaking research was attracting little attention, I contacted Dr. Eriksen and interviewed him via email. This post contains a summary of his hypothesis, which I’ve tried to present in everyday language.

Other posts contain 1) the interview, which contains considerable new information about his hypothesis, and 2) my understanding of how Eriksen’s model fits with other research—and with my experience. Continue reading →

[Update from Sept. 2018 here!] In two other posts, I summarize Dr. Willy Eriksen’s hypothesis for the cause of and cure for myalgic encephalomyelitis, aka chronic fatigue syndrome (ME/CFS), and I interview Eriksen. Here I—a well-educated sufferer but no biologist or physician—consider this model in the light of other research and my own experience. In other words, I’m thinking about it in print. While I have questions and reservations, I think Eriksen might be right about some important aspects of ME/CFS. Continue reading →

On Sept. 17, 2010, I fell ill and, barring a medical miracle, will never fully recover. It took more than three years to get a diagnosis: “chronic neuroimmune dysfunction,” better known as chronic fatigue syndrome or myalgic encephalomyelitis. Since it’s ME/CFS Awareness Day, I thought I’d share some basic information about this disease. Continue reading →