Voices for Ability Radio interviews the Canadian CdLS Foundation President & Founder about CdLS and the current work of the Foundation.

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Thanks for listening to CdLS Connections brought to you by the Canadian CdLS Foundation.

Stay connected with our community at www.canadiancdlsfoundation.com and follow us on social media for more stories, support and updates. Together, we're building awareness and connection for everyone affected by Cornelia de Lange Syndrome.

(c) Canadian CdLS Foundation. All Rights Reserved.

Join us for a previously recorded webinar with Kelly Hall-Berenesky to learn about her daughter Grace's Autism Assistance Service Dog.  Grace lives in Red Lake, Ontario and was born with CdLS and as with many individuals with CdLS, anxiety can be a huge challenge that often times results in responsive behaviours.  Learn about the process for applying for a service dog, its challenges and benefits and how Sandro has become a part of Grace's entire family and community.

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Support the show

Thanks for listening to CdLS Connections brought to you by the Canadian CdLS Foundation.

Stay connected with our community at www.canadiancdlsfoundation.com and follow us on social media for more stories, support and updates. Together, we're building awareness and connection for everyone affected by Cornelia de Lange Syndrome.

(c) Canadian CdLS Foundation. All Rights Reserved.

Jenn Evans is a Physiotherapist, certified Rebound therapist and a volunteer Clinical Advisor for the Canadian CdLS Foundation.  Jenn shares with us a form of therapy that is fun, beneficial and relatively new in the Canadian landscape. Join us to learn more about the benefits of Rebound Therapy.

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Support the show

Thanks for listening to CdLS Connections brought to you by the Canadian CdLS Foundation.

Stay connected with our community at www.canadiancdlsfoundation.com and follow us on social media for more stories, support and updates. Together, we're building awareness and connection for everyone affected by Cornelia de Lange Syndrome.

(c) Canadian CdLS Foundation. All Rights Reserved.

Join us as we share the grief journey of a CdLS diagnosis. Carmen practices soul medicine in Calgary, AB and is a mother of three children. Her middle child Eli was born with CdLS and shares her story of receiving the diagnosis and how that has impacted her practice. Learn more about Carmen at www.carmenwilde.ca

If you or your family member has been diagnosed with CdLS and you would like support, please contact [email protected]

Send us a text

Support the show

Thanks for listening to CdLS Connections brought to you by the Canadian CdLS Foundation.

Stay connected with our community at www.canadiancdlsfoundation.com and follow us on social media for more stories, support and updates. Together, we're building awareness and connection for everyone affected by Cornelia de Lange Syndrome.

(c) Canadian CdLS Foundation. All Rights Reserved.

Join us for a conversation with Sarah Strathy-Alie, SLP as we discuss the role of Speech Language Pathology in the life of an individual with CdLS. This is Part 2 of our conversation.

Send us a text

Support the show

Thanks for listening to CdLS Connections brought to you by the Canadian CdLS Foundation.

Stay connected with our community at www.canadiancdlsfoundation.com and follow us on social media for more stories, support and updates. Together, we're building awareness and connection for everyone affected by Cornelia de Lange Syndrome.

(c) Canadian CdLS Foundation. All Rights Reserved.

Join us for a conversation with Sarah Strathy-Alie, SLP as we discuss the role of Speech Language Pathology (SLP) in the life of an individual with CdLS. Sarah Strathy-Alie is a SLP in Toronto where she sees children and adults both in the Catholic School Board but also at her private practice where she sees individuals with CdLS.  She is also on the Clinical Advisory Team of the Canadian CdLS Foundation and provides consultation and treatment to individuals with CdLS.

Send us a text

Support the show

Thanks for listening to CdLS Connections brought to you by the Canadian CdLS Foundation.

Stay connected with our community at www.canadiancdlsfoundation.com and follow us on social media for more stories, support and updates. Together, we're building awareness and connection for everyone affected by Cornelia de Lange Syndrome.

(c) Canadian CdLS Foundation. All Rights Reserved.