This page contains questions frequently asked about the Williams Syndrome Association.
Q. My child has just been diagnosed with Williams syndrome. How can the WSA help me?
A. The WSA provides support to families in many ways: First, it is important to note that when you call the WSA National Office, or a regional or state representative, you will be speaking with the parent of a child with Williams syndrome. Each of us has made a commitment to helping you through the hard times as well as sharing in the joy of each child�s triumphs.
Q. What are some of the current WSA activities? [back to top]
A. The WSA currently:
- Advances the public awareness of Williams syndrome
- Helps people with Williams syndrome reach their highest attainable goals
- Educates medical and educational professionals about Williams syndrome
- Maintains an extensive library of articles and tapes on Williams syndrome; is the largest clearinghouse for information regarding Williams syndrome
- Provides information on the most up to date educational strategies and medical treatments for Williams syndrome
- Actively supports research on Williams syndrome
See the WSA programs page for more details.
Q. How is the Williams Syndrome Association supported? [back to top]
A. The Williams Syndrome Association is a 501(c)(3) non-profit, tax-exempt corporation. It derives support primarily from private donations and fund-raising projects.
Q. How can I support the Williams Syndrome Association? [back to top]
Q. How can I get more information about the Williams Syndrome Association? [back to top]
A. There are many ways to reach the national WSA office. Call us toll-free at: 1-800-806-1871 or, for more ways to contact us, see our Contact information page.
