The Williams Syndrome Association is a nonprofit organization that strives to enrich the lives of individuals and families affected by Williams syndrome and similar conditions through support, research and education. The Williams Syndrome Association (WSA) is the most comprehensive resource for people and families living with WS as well as doctors, researchers and educators. The WSA provides the resources and referrals that families need, and a strong and supportive community with which to connect throughout that child’s life. We create a road map to help families navigate challenges – providing answers to common questions, a step-by-step guide, information about WS clinics across the country and best practices for age-appropriate interventions.