Williams Syndrome Association
WSA: research, programming and support for families and caregivers affected by Williams syndrome.
The Williams Syndrome Association (WSA) was formed in 1982 by, and for, families of individuals with Williams syndrome to provide the resources and referrals you need now, and a strong and supportive community for a lifetime.
It is the most comprehensive resource for people and families living with Williams syndrome as well as doctors, researchers and educators. The WSA provides resources, support and the latest medical information to help your child today and throughout his/her life. By joining, you’ll become part of the largest organization dedicated to improving the lives of people living with Williams syndrome.