Our Members

Their activities include raising awareness through seminars, conferences, campaigns and advertising; and engaging with medical professionals and their associations, Government, charities and other organisations to advocate for families with Lynch syndrome.

The Maternity Coalition is Australia's National Maternity Consumer Organisation. We believe that birth matters in Australia today.

The ME/CFS/FM Association - Queensland provides information, support and counselling to patients with chronic fatigue syndrome/fibromyalgia and their carers, and raises funds for medical research into the illnesses.

As the national peak body for people living with MS in Australia, they campaign about important issues on behalf of our community by working closely with our state societies, national advocates and MS Research Australia, to ensure their submissions and work are based on the latest evidence. They advocate across all stakeholders, governments and communities on behalf of our state and territory member organisations to represent people who are diagnosed with the disease, their carers and the broader MS community.

The National Association of People Living with HIV/AIDS, Australia (NAPWA) is the peak national non - government organisation representing people living with HIV/AIDS community based groups in Australia. NAPWA is the only national association advocating and representing specifically on behalf of people living with HIV/AIDS, and it ensures that people living with HIV/AIDS are central to the Australian response to the HIV/AIDS epidemic.

The National Stroke Foundation is a not-for-profit organisation that works with stroke survivors, carers, health professionals, government and the public to reduce the impact of stroke on the community. We are the voice of stroke in Australia.

The National Stroke Foundation is a not-for-profit organisation that works with stroke survivors, carers, health professionals, government and the public to reduce the impact of stroke on the community. We are the voice of stroke in Australia.

Our mission is to improve the quality of life of people living with pain, their families and carers, and to minimise the social and economic burden of pain on individuals and the community. We advocate for improved health policy and practice; we promote access to education and training for health professionals; and we work to raise awareness of chronic pain within the community through media and education campaigns, to help reduce the stigma of this silent epidemic.

Our mission is to improve the quality of life of people living with pain, their families and carers, and to minimise the social and economic burden of pain on individuals and the community. We advocate for improved health policy and practice; we promote access to education and training for health professionals; and we work to raise awareness of chronic pain within the community through media and education campaigns, to help reduce the stigma of this silent epidemic.

Our mission is to improve the quality of life of people living with pain, their families and carers, and to minimise the social and economic burden of pain on individuals and the community. We advocate for improved health policy and practice; we promote access to education and training for health professionals; and we work to raise awareness of chronic pain within the community through media and education campaigns, to help reduce the stigma of this silent epidemic.

Parkinson’s Australia represents over 70000 Australians living with Parkinson’s Disease through advocating their needs and interests to all levels of government. Our member organisations provide direct support to people with Parkinson’s, their families and carers. We also seek improved funding for services, research and awareness raising to improve the quality of life of these people. Our support group services can be accessed through our website or by calling 1899 644 189.