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CdLS Connections

Navigating the challenges & triumphs of Cornelia de Lange Syndrome (CdLS) and where we explore, learn, and share everything related to CdLS. We will learn from families, clinicians, researchers & educators and those exploring new frontiers relevant to the CdLS community.
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Host

Jenni Glad Timmons

Jenni Glad Timmons is the President and Founder of the Canadian CdLS Foundation and also mom to a young adult daughter who was born with Cornelia de Lange Syndrome (CdLS).

https://www.linkedin.com/in/jenni-glad-timmons-07a38420b/
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