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The Williams Syndrome Changing Lives Foundation is a non-profit foundation centered on increasing Williams syndrome awareness, increasing education for families, the public, physicians and therapists.
The Williams Syndrome Changing Lives Foundation was formed to enhance the lives of children and adults living with a diagnosis of Williams syndrome by providing needed financial assistance with medical, therapeutic, recreational needs and other developmental resources. In addition, the Williams Syndrome Changing Lives Foundation provides support for individuals, parents and families through support, outreach and sponsored functions.
Inspired by my youngest son, Keith, who was diagnosed with Williams syndrome and autism, I formed Williams Syndrome Changing Lives Foundation with the vision of providing financial assistance and support to individuals/families affected by Williams syndrome. Penny Perez
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