• Changes to the CAWS Music Scholarship

    Changes to the CAWS Music Scholarship

    There are exciting changes to the Music Scholarship offered by CAWS.

  • Help a child reach his full potential

    Help a child reach his full potential

    A child can be born with Williams Syndrome anywhere.
    You can help us support families everywhere in Canada.

  • The sky’s the limit

    The sky’s the limit

    When you support Williams syndrome education, awareness, advocacy and research, you help people like Alma reach their full potential.

Learn More

  • Latest E-Newsletter

    Newsletter February 8, 2023

    Every month, CAWS sends out a new email newsletter filled with information, family stories and updates from the CAWS team. If you aren’t on the list, you can subscribe here! Honouring Siblings This cherished picture of my son and daughter was taken over three...

    read More
  • williamssyndrome.ca // what is Willliams syndrome

    What is Williams Syndrome?

    Williams Syndrome August 20, 2015

    What is Williams Syndrome? Williams syndrome is a rare genetic condition that is present at birth. It is caused by a random genetic deletion and can affect anyone. It occurs equally in males and females, all cultures and to birth parents of all ages....

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  • Williams Syndrome Frequently Asked Questions

    Frequently Asked Questions

    Williams Syndrome August 20, 2015

    Frequently Asked Questions Learn more about Williams Syndrome.    

    read More

About CAWS

Making a difference for Williams Syndrome in Canada

About CAWS

The Canadian Association for Williams Syndrome (CAWS) provides support to Williams syndrome 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 Williams syndrome. We are a small but mighty National Registered Charity, whose impact can be felt in tiny towns and big cities across Canada.

Learn More Or
Email Us At info@williamssyndrome.ca

Our Directors

    • Melanie Côté

      Ontario Director, Media Chair and National Walk Coordinator

      Melanie, the President of CAWS has been involved with the organization since 2013. She and her husband Chris have two children, one who was born with WS.

    • williams syndrome Canada Nathalie Saskatchewan Director

      Nathalie Bérubé

      Saskatchewan Contact

      Originally from Quebec, Nathalie now lives in Warman, Saskatchewan (just 20 min North of Saskatoon) and is a mother of two: Paul (WS) and Mélina.

    • williamssyndrome.ca // New Brunswick Director family

      Michelle and Blais Dobbin

      New Brunswick Director

      Blaise and Michelle Dobbin live in southeastern New Brunswick region with their two kids Megan and Nolan (WS).

Testimonials

What people Says About Us

  • “I guess what makes the CAWS such a fantastic nest to all of us is the people who runs it . They have the passion , the drive and the pride . Thank you for making this journey a bit easier by sharing and connecting WS families from coast to coast .”

    Talina’s Parents

  • The comfort that comes from someone simply saying “I’ve been there too” should never be undervalued.

    Thank you CAWS for welcoming Sophia and our family into your family.

     

    Rick C, Sudbury, ON

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