About LDSA
The London Down Syndrome Association was originally an initiative by a group of parents who were attending the Child and Parent Research Institute’s support group. Since it’s creation in 1987, the LDSA has committed to “Enhance the Quality of Life for All Individuals who have Down Syndrome”. LDSA is a not for profit, charitable organization.
The LDSA set out with a number of ongoing goals:
- Raise Down Syndrome Awareness
- Provide Information Resources
- Develop Community Partnerships
- Support Individuals, Families & Friends
- Provide Social Opportunities
From our modest beginnings, the LDSA has evolved into a structured and directed organization. A Constitution and By-Laws has been developed to ensure fair and equitable practices as well as making sure our goals are met. At the head of the association is an Executive Committee (Board of Directors), who directs the activities of the association with input from the membership as a whole.
We are an association of people with Down Syndrome, their families and friends, and we have in our numbers several professionals, organizations, and companies who are also interested in furthering the goals of LDSA. Lastly, we are a group of dedicated volunteers who are passionate about accomplishing the goals of the association.
We pride ourselves in the fact that, as a not for profit charitable organization, all funds generated are directed entirely into our programs and services.