Paradigm Shift for Long COVID Patients (and people with ME/CFS)? The dramatic announcement that Congress is going to appropriate over a billion dollars (a billion dollars!) to study the COVID-19 long haulers was just one sign that long COVID is being taken seriously....
Emily Taylor of Solve ME/CFS Initiative reported that Congress has approved $1.15 billion (yes that’s a billion with a “B”) for the NIH to fund long-COVID research and clinical trials. $100 million will specifically be used for the rapid acceleration...
A riff on Dr. Peter Rowe’s presentation at the 2020 Dysautonomia International Conference (note that I expand on many of Rowe’s points; i.e. not all the words are his.) Lauren Stiles, the founder of Dysautonomia International, has long believed that the...
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