Williams Syndrome Association (WSA)
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.
Camps
Each summer (and at a special adult camp in March!) approximately 250 youth and teens and adults with Williams syndrome enjoy camp weeks designed especially for them, at WSA-sponsored camps. The camps are busy, happy, and enriching places with many activities and specialized programs
| Age Groups |
|
Last Updated: 01/31/25
