Tomorrow, February 10, 2015, the IOM will release the Report on the Diagnostic
Criteria for Myalgic Encephalomyelitis/Chronic Fatigue Syndrome at 11am ET. The event will be available via live webcast at this link.
If you are unfamiliar with the IOM process, here is a summary of what they've been working on that I posted last year.
This should be interesting! So glad this one is in the morning and not during nap time - I should be able to tune in.
I have had Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) since March 2002. Both of my sons also got ME/CFS at ages 6 and 10. Our younger son fully recovered after 10 years of mild illness. Our older son still has ME/CFS and also has Lyme disease plus two other tick infections. This blog is about how our family lives with chronic illness, with a focus on improving our conditions and enjoying our lives in spite of these challenges.
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