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Who We Are

Est. 1983

Our Beginnings

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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.

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Our Mission

The London Down Syndrome Association raises funds to provide responsive, compassionate support services to children, youth, adults and families living with Down Syndrome – including:

Financial Assistance
Support Programs & Services
Community Collaborations
Educational Opportunities
Resources
Social Opportunities
Public Awareness
Advocacy
Our Team

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
Email
KAREN LUBEK

Volunteer Coordinator

MEGAN ADAIR

Tee-21 Chair

TERRI MANNING & NORM ASKEW

Annual Gala Co-Chairs