Driving research of Myalgic Encephalomyelitis / Chronic Fatigue Syndrome (ME / CFS),
Post Treatment Lyme Disease Syndrome (PTLDS), Fibromyalgia and Long Covid

Archives: Symposium Questions

Is the IDO genetic mutation going to be checked on hundreds or thousands of patients to see if its universal in ME patients?

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Is the IDO genetic mutation going to be checked on hundreds or thousands of patients to see if its universal in ME patients?

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REQUEST…I am a sufferer. I want to help you raise money. It would help immensely to have a 1-pager or a brief video that says

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What kind of genetic testing would be useful to get? Where can we get whole exome testing? Are companies like Blueprint a good way to

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Is there anyway to contact speakers personally with questions that have not been selected to be answered in the webinar?

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Is there any connection between the liver mitochondria and CFS? In particular dysfunction in fatty acid metabolism? Does this relate to fatty liver in any

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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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