The community of families impacted by Williams syndrome who are members of the WSA is between 3,000 and 4,000, but in your immediate community you may be the only family with a child with Williams syndrome, or one of just a few.
The Williams Syndrome Association is organized into 19 regions across the United States. Each region works to provide resource information and social and educational opportunities to its members. Each region is led by local volunteer regional chairs (parents and grandparents who can provide resources and information) and supported by local committee volunteers who work hard to facilitate annual gatherings such as picnics, conferences and fundraising events.
Using the tool below, select your state to find name(s) of your regional chair(s), e-mails, and phone numbers as well as separate calendars for events and regional Facebook pages to join. Make sure you're a member of the WSA so you are on our email list for communications.