Building advocacy networks for people
so that they have a good life even after their parents are no longer here to stand up for them
Building advocacy networks for people
so that their families have peace of mind about the future
Building advocacy networks for people
so that they are empowered to realise their aspirations and contribute to their community
Building advocacy networks for people
so that they form intentional friendships that broaden and enrich their lives
Building advocacy networks for people
so that they develop stronger links in the wider community
Building advocacy networks for people
so that they are as fulfilled and happy as they can be
We’ve been encouraged to read about the Down Syndrome Research Programme, a 41-year study based at the University of Queensland’s School of Education. This is the world’s longest running and most complete study of its kind. It started by recruiting around 40 children born between May 1976 and December 1978. Since then over 200 families have contributed to the research. The programme has expanded to include many other studies on Down’s Syndrome.
"This research has affirmed that people born with Down Syndrome can look forward to a good life with the opportunity to make valued contributions to their families and the community," says Dr Rhonda Faragher, the director of the programme.
It used to be thought that the language and literacy skills of people with Down’s Syndrome would plateau in early adolescence, but the research shows otherwise. This has led to Latch-On, an award-winning two-year programme of literacy and technology teaching and learning for adolescents with Down’s Syndrome and/or other learning disabilities. Latch-On has been running for 15 years in Australia and has also been licensed to organisations in Canada and Ireland. One of the areas currently being studied is mathematics: what teaching approaches are being used for students with Down’s Syndrome in mainstream secondary classes?