A personal letter to the NIH team researching ME/CFS about their PEM study, 2020

Hmm. Don't know why I bothered really. The presentation was OK, they just went through their key so findings and said how it had helped with very basic stuff about designing the main NIH study, like building in rest times, which they could have learned by talking to any person with ME. My question wasn't asked. They seemed very satisfied with their research.
 
Did you catch how one researcher called it "P-E-M" and the other "pm" ?

It was pretty basic. But the qualitative aspect, it seemed a good thing.
 
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