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The following resources are for caregivers, and people living with ME/CFS, Long COVID, and related multi-system chronic complex diseases (msCCD). Please see the menu item
The following resources are for caregivers, and people living with ME/CFS, Long COVID, and related multi-system chronic complex diseases (msCCD). Please see the menu item
(Press Release by CDC) The Centers for Disease Control and Prevention (CDC) today released an updated website for healthcare providers about myalgic encephalomyelitis/chronic fatigue syndrome (ME / CFS). Stethoscope
by Sarah Wells “Imagine you had the worst flu ever, but it never went away,” said Linda Tannenbaum, a clinical laboratory scientist, to a crowd
People impacted by ME / CFS are always glad to see the news media give accurate attention to the disease and the struggle for appropriate federal research
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