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.
Williams syndrome is a rare genetic disorder caused by the deletion of the long arm of chromosome 7. A random genetic mutation (deletion of a small piece of chromosome 7), rather than inheritance, most often causes the disorder and is present at birth.
Check out http://wschanginglives.org! Williams Syndrome Changing Lives Foundation assists children and adults diagnosed with Williams syndrome with medical, therapeutic, recreational and developmental needs.
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You know Black Friday and Cyber Monday, but do you know about Giving Tuesday? It's the day to give back. Please consider donating to Williams Syndrome Changing Lives Foundation to help us continue to Change Lives. To donate, you may go to http://lnkd.in/dfXR8CE
When your child turns 18, a child becomes an adult in the eyes of the law. This means you have no parental rights or decision making authority regarding education, medical, financial issues and more.
Williams Syndrome Changing Lives Foundation's insight:
Free webinar from our partners at The IEP Advocate!
When... Tuesday, Nov 12th 9:30 to 11:00 a.m.
Can't make the live event? Register and they will send you a recording!
When your child turns 18, they become an adult in the eyes of the law. This means you have no parental rights or decision making authority regarding education, medical, financial issues and more. This is true even for developmentally disabled children.
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