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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Thursday, April 14, 2011
NIH State of the Knowledge Videocast Posted
For all of you who were waiting to watch some (or all) of last week's NIH ME/CFS State of the Knowledge Workshop, the videocast has been posted (just scroll down a bit to April 7-8). If you want to zero in on certain presentations, you can refer to the meeting agenda to help find the sections you want.
As always, thanks so much, Sue, for providing this information for us.
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