Our Mission

To enhance the quality of life of those impacted by ectodermal dysplasias through education, service, and supports while serving as a national information and support resource.

Our Vision

The Canadian Ectodermal Dysplasias Syndromes Association (CEDSA) will act as the national information and resource centre on provincial and territorial funding programs, medical expertise, ongoing research and support groups. Working with established ectodermal dysplasias associations around the world, CEDSA will support research towards a cure, raise awareness of EDS and connect children, youth, family and friends seeking support and a place to share information.