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Liz goldberg

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Williams Syndrome Association
November 15, 2012

Our son was 14 months old when we received his WS diagnosis. Without the WSA, I don't know what we would have done! They sent me a Welcome packet, explaining WS, and put us in touch with other families in our area with the same diagnosis. They also put us in touch with top WSA specialists, helped with school, held conferences for us explaining what's going on with research for WS. They are a Wonderful Organization! I would like to Thank them for being there for our son for the past 15 years!

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