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This is a brief post that draws on the analytical approach from the methodology used in Mast Cell Activation Syndrome and Multiple Chemical Sensitivity. Atypically, we are able to determine which probioti...
This evening on NPR News, I saw their story on Long COVID and pending work. You may view the segment here. From watching ME/CFS research for several decades, “I wept” for Long COVID patients — I do not expect any of this planned work to produce relief to patients.
In the past, when I had active ME/CFS. I could describe it as a flare sufficient to put me on disability. I would sit on the computer playing a variety of simple puzzle games. AAs the flare eased and my cognition improved, I began to find those games boring and moved on to more mentally challenging puzzles.
href="https://cfsremission.com/wp-content/uploads/2025/09/i...27 years ago, I was diagnosed with ME/CFS. Even as far back as the early 1970s, while at university, I experienced severe cognitive difficulties—including a sudden decline from managing triple honors to simply trying to finish my degree. At the time, my physician correctly attributed these issues to stress, though the biological mechanism was unclear. Today, ...
