Support, Advocacy, Education and Community for those affected by Williams Syndrome

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About CAWS

Making a Difference for Williams Syndrome in Canada

The Canadian Association for Williams Syndrome (CAWS) provides support to  Williams syndrome (WS) individuals, their families and caregivers, coast-to-coast. Our  grassroots, parent-volunteer run organization is on a mission to spread awareness,  raise funds, support research and connect families touched by WS.  We are a National Registered Charity, whose impact can be felt  in towns and cities across Canada.

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Williams Syndrome Facts

DID YOU KNOW  

  • Williams Syndrome affects 1 in 7,500 - 10,000 people worldwide.
  • Williams Syndrome is known to occur equally in both males and females and in every culture. 
  • Williams syndrome is caused by the spontaneous deletion of 26-28 genes on chromosome #7 at the time of conception. 

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Become a Member

We are a small but mighty National Registered Charity, whose impact can be felt in tiny towns and big cities across Canada.

If your family member has recently received a Williams syndrome diagnosis or if you’re supporting someone with Williams syndrome, we hope you’ll join us

  • Access to Support and Resources: Joining the Canadian Association for Williams Syndrome provides access to a wealth of information, resources, and support networks specifically tailored to individuals with Williams Syndrome and their families. 
  • Advocacy and Awareness: By becoming a member of the association, you contribute to a collective voice advocating for increased awareness, understanding, and support for Williams Syndrome within Canada. Your membership can contribute to a stronger voice for positive change and improved services for individuals with Williams Syndrome.
  • Community and Networking: Joining the association allows you to become part of a supportive and inclusive community. Connecting with other families, individuals with Williams Syndrome, and professionals in the field can create a sense of belonging and camaraderie. 

Connect with Us

Walk For The CAWS

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Our Stories

Meet Kayla

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Family Support Network

Are you looking for ways to connect with other parents/caregivers? Join our WSA Family.

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Make a real difference for someone living a rare life

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