VATTA (Canadian Down Syndrome Society), 28th July 2014.
Have you ever wondered what prenatal testing means to people with Down syndrome? A group of nine adults with Down syndrome want to share their overlooked perspective on this topic, in the film What Prenatal Testing Means To Me, available to watch on the Canadian Down Syndrome Society’s website.
The film stars VATTA (Voices At The Table Advocacy), the Canadian Down Syndrome Society’s self-advocate-led steering committee. These remarkable adults, ranging in ages 22 to 43, reflect on their hopes and fears for the future of Down syndrome in Canada and around the world.
Prenatal testing is a complex and controversial subject. VATTA’s view is simple: If people have fair and balanced information about Down syndrome, and take the time to know and learn more about people with Down syndrome, they will be able to make a better choice for themselves and their families. VATTA wants everyone to “See the Ability” and not believe misconceptions or fears about Down syndrome.
The film was originally presented as a session at the 2014 Canadian Down Syndrome Conference in response to a growing number of concerns by parents and expectant parents regarding prenatal testing.
VATTA’s mission is to help all Canadians “See the ability.” VATTA helps self-advocates use their voice and stand up for what they believe in. VATTA has been part of the Canadian Down Syndrome Society since 2005.
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