Our Beginnings
Established in 1983 the London Down Syndrome Association evolved from a Parent Support Group through the Child and Parent Research Institute (CPRI) in London, Ontario. The London Down Syndrome Association known as LDSA, is a registered charity located in London Ontario, providing support within the counties of Elgin, Huron, Middlesex, Oxford and Perth. This dedicated group of parents desired to create an organization that would provide emotional and social opportunities for families while raising funds to provide much needed programs and support services.
The LDSA is led by a volunteer Board of Directors – comprised of parents and community members. The Board of Directors work tirelessly to support the children and families in our community and is dedicated to making a lasting impact. As part of the organization’s Vision and Mission, the LDSA advocates and raises awareness and recognizes the contributions made by people with Down Syndrome. Today, the LDSA continues its long history of advocating for dignity, equal rights and a better life for all persons with Down Syndrome.
The London Down Syndrome Association raises funds to provide responsive, compassionate support services to children, youth, adults and families living with Down Syndrome – including:
Board of Directors
& Volunteer Support
Board of Directors
DAN TWIST
Chair
NORMAN ASKEW
Vice Chair
RHONDA ASKEW
Treasurer, Director of Programs, SEAC Representative (TVDSB)
NANCY DELORY
Secretary
VACANT
SEAC Representative (LDCSB)
SHANA MECHEFSKE
Director
GREG KEANE
Director
AARON LALANDE
Director
JOLIN PAYNE
Director
SUSANA MARTINEZ DE RIVERO
Director
Volunteer Support
Name
KAREN LUBEK
Volunteer Coordinator
MEGAN ADAIR
Tee-21 Chair
TERRI MANNING & NORM ASKEW
Annual Gala Co-Chairs