The Williams Syndrome Association (WSA) is the comprehensive resource for individuals and families living with Williams syndrome, as well as for doctors, researchers, and educators. Established in 1982 by and for families of individuals with Williams syndrome, the WSA provides resources, support, and the latest medical information to help children and adults with Williams syndrome thrive. Their mission is to advance the interests of individuals with Williams syndrome by providing programming and resources, supporting research, promoting partnerships, and ensuring a strong community.

The WSA offers information, emotional support, and programs for individuals with Williams syndrome at every stage of life, from early childhood through adulthood. They strive to increase public awareness and understanding of Williams syndrome and support research into various issues related to the condition. With a dedicated staff and volunteers nationwide, the WSA is committed to improving the lives and advocating for the full inclusion of individuals with Williams syndrome in educational, work, and community settings.

Join the WSA to access support, connect with others, and navigate the challenges of Williams syndrome