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First, thank you for doing this for all of us to learn!!!!!!

So many little things in each of the avenues of research resonate with what I experience as a sufferer (a healthier sufferer but still significantly affected). Does it help the researchers/contribute to the research in any way, if we share and emphasize what those symptoms are as it might lead research to go in one way or the other?

(Example — not being able to tolerate aerobic exercise at all versus anaerobic). Collection of this information would be a challenge, but if it were worth it, I would work towards that!

PS. And I am going to put ice on my head to cool off my brain!!!

Thanks again. Elaine

Myalgic Encephalomyelitis / Chronic Fatigue Syndrome (ME / CFS) Post Treatment Lyme Disease Syndrome (PTLDS), Fibromyalgia Leading Research. Delivering Hope.Open Medicine Foundation®

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