The Australian Sjögren's Syndrome Association

As there is no research undertaken in Australia, Ms Norton contacted the American Sjögren's Syndrome Foundation and became their representative in Australia. They sent out books, resources such as brochures, flyers and posters that could be used until TASSA could get their own sponsored.

The Association is set up to provide:

- Support, information and education to individuals, carers, and their family and friends suffering from any aspect of Sjögren's Syndrome;

- an awareness of the syndrome to healthcare providers, dentists, eye specialists, the general public and health care funds e.g. MBF and HCF;

- Funds for research into cause, prevention, treatment and cure of the disease and give individuals the education and coping mechanisms needed to deal with the disease on a daily basis;

- a clearing house for medical information and a recognised national advocate for people with Sjögren's Syndrome.