Want an opportunity to help ME/CFS research from your couch or bed?
This lovely young woman from George Washington University whose aunt has CFS has set up a charity volleyball tournament to raise money for ME/CFS research. Check out her website to read all the details and hear from an adorable little boy who wants you to help his Grammy.
You can donate directly from the website to help fund this great charity event up until April 21, the date of the tournament. I just did!
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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