The Association was formed in 1984 with the principal aim of helping families of children with Down syndrome, and in particular, to help children to realise their full potential. The types of people who join the Association are parents and/or guardians of children and adults with Down Syndrome; adults with Down Syndrome; and professionals, or persons, interested in the welfare of people with Down Syndrome generally.

FUNCTIONS OF THE ASSOCIATION

• To advise the community of the positive role that people with Down syndrome can play within society

• To advocate for the interests of people with Down syndrome

• To promote the inclusion of people with Down syndrome into the community

• To ensure new parents of babies with Down syndrome have all available information, to assist them during the early period of their child's life.

• To provide support and assistance to all parents of children with Down syndrome

• To advise families of children with Down syndrome of the medical, educational, financial, social and legal benefits to which they are entitled

• To campaign for educational facilities and programmes to be available for all people with Down syndrome in Tasmania, including early intervention programmes, appropriate ongoing education and vocational training

• To maintain a library on matters relating to Down Syndrome

• To lobby for accommodation, recreation and support facilities for people with Down syndrome

• To lobby both the government and the community to accept financial, educational, medical and occupational programmes for the benefit of people with Down syndrome