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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Tuesday, February 04, 2014
WEGO Health Activist Award Nomination
I was very honored to hear last month that this blog had been nominated for a WEGO Health Activist Best in Show Award! Unfortunately, between my own challenges and my sons' medical problems, I haven't had time to even tell anyone about it until now.
Anyway, the award nominations are open for voting now, so if you have found my blog useful, you can vote for me at this link.
And thank you for eight years of kindness, encouragement, and support!
Hi Sue,
ReplyDeleteCongratulations! I went to the site and you can't vote on a particular person. However, they are looking for a panel of judges.
Beatrice
Thanks for trying, Beatrice! I think I was VERY late in getting the word out - people were able to vote the day I posted this, but then the next day the voting button was gone. Oh, well - that's just the way things have been around here lately!
DeleteSue