Resources and updates from the Web on Williams Syndrome
Saturday, July 2, 2011
ABC News Report (20/20) on Williams Syndrome (in two parts)
1 comment:
Anonymous
said...
Thanks for posting this story. My 20 year old daughter lives with WS. She out fishes me every time. She never met a stranger. I have been a member of Terri's WSA since the begining it's been a real joy and challenge being around these folks. I learn from them every day.
Identified more than 40 years ago, Williams syndrome occurs in an estimated one in 20,000 births worldwide. It arises from a faulty recombination event during the development of sperm or egg cells. As a result, almost invariably the same set of about 20 genes surrounding the gene for elastin is deleted from one copy of chromosome seven, catapulting the carrier of the deletion into a world where people make much more sense than objects do. Despite a myriad of health problems and a generally low IQ, people with Williams syndrome are loquacious, sociable, and very empathetic.
Why This Blog?
I am a Dad to a great little WS person and love doing all I can to understand his world and love him better. Since information on WS is fairly rare, I thought I would share whatever I found of interest. Plus, if you know my kid, here is a great way for you to understand him better!
1 comment:
Thanks for posting this story. My 20 year old daughter lives with WS. She out fishes me every time. She never met a stranger. I have been a member of Terri's WSA since the begining it's been a real joy and challenge being around these folks. I learn from them every day.
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