Annette Whittemore and Dr. Donnica Moore appeared yesterday on Nevada Newsmakers, talking about pediatric CFS. I think this is the beginning of their efforts to bring more attention to how CFS affects kids and teens.
You can listen to their interview at the Nevada Newsmakers website (it's listed under Tuesday, May 18). It takes a few minutes to download the video - and there are a bunch of local ads to get through! - but it's worthwhile.
Busy, busy here (and feeling rotten) - my mom and her husband come in today to stay for a couple of days and I'm hoping to get to my book group tonight. I'm trying to figure out how to manage two dinners with the least amount of work!
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.
3 comments:
Sue - thanks for the great info, as always. I talked you up in my post today, btw, because you are the best!
I think you have the biggest family ever! LOL
I hope you are able to rest some.
"Two dinners with the least amount of work!" Take out anyone! ha ha
Hi Sue,
I hope you begin to feel a little better soon. It does sound like you're incredibly busy. Maybe things will be well paced so that you can relax and enjoy the weekend with your mom.
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