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.
National Heart Foundation of 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.
Nepean Blue Mountains Community Advisory Committee
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.
Palliative Care Australia is the national peak body for palliative care.
Palliative Care Australia represents all those who work towards high quality palliative care for all Australians. Working closely with consumers, our Member Organisations and the palliative care workforce, we aim to improve access to, and promote the need for, palliative care.
We believe quality palliative care occurs when strong networks exist between specialist palliative care providers, primary generalist, primary specialist and support care providers and the community.
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.
The Post-Polio Network (NSW) is a self-help self-funded volunteer organisation run by polio survivors. It provides information and support about the late effects of polio to polio survivors, their families and the health professionals who care for them.
Queensland Bioethics Centre
Queensland Voice for Mental Health was launched as a united voice for consumers and carers to actively promote the health and well-being of all Queenslanders through advocacy, co-operation and education.
RVA is Australia's national organisation advocating for those who live with a rare disease. RVA provides a strong common voice to promote for health policy and a healthcare system that works for those with rare diseases. RVA works with governments, researchers, clinicians and industry to promote research, diagnosis, treatment and services for all rare diseases in Australia.
The Sleep Apnoea Association ACT is a self help support group for sufferers of sleep disorders.
The Immune Deficiencies Foundation Australia (IDFA) is a not-for-profit health promotion charity raising awareness and caring for people who have Primary (Genetic) and Secondary (due to chemotherapy and other treatments/ or autoimmune illness) Immune Deficiencies (PIDs).
Tuberous Sclerosis Australia is a volunteer run organisation which helps families living with TSC through phone, email and online support services, educational materials and events, facilitation of peer support and funding of TSC research in Australia and New Zealand.