Every 3-5 years, the WSA creates a strategic plan to guide the organization. We use this strategic plan to guide our vision and programming. In our current 5 year plan, our priorities are on finding ways to promote and facilitate meaningful inclusion in all environments and provide support to all families throughout the lifespan. In addition, we will continue our efforts to fund high impact research and ensure the growth of research expertise in Williams syndrome. Finally, we recognize that we cannot succeed in any of these areas without increasing our capacity and building our infrastructure.
