It takes a community to raise an individual with Williams syndrome. Many of those within your community will be family, friends, and professionals who you know personally. There will be many others who you will never meet but who can have a profound impact on your and your child’s journey with Williams syndrome. They are the many resource providers who you will find listed below – educators, physicians, surgeons, researchers, therapists…the list is long. Come back often – these resources are available 24/7!
Use one or more of the filters or browse by life stage below.
The Williams Syndrome Association (WSA) does not provide medical or legal advice or services. The articles, books and links above are not a recommendation, referral, or endorsement of any resource, therapeutic method, or service provider and does not replace the advice of medical, legal, or educational professionals.
Your input is invaluable as we gear up for the WSA's 2024 Williams Syndrome Convention! We aim to include everything you want to learn about and participate in. Submit your completed survey by September 29th.