Working towards a world without MND.
To provide and promote the best possible care and support for people living with MND.
The objectives of MND Victoria are:
- To provide the best possible care and support for people living with MND.
- To collect and share the best available advice on living with MND.
- To create and foster links between people living with MND by providing opportunities for interaction.
- To raise awareness of MND and the needs it creates.
- To develop and maintain relations with MND Associations within Australia and overseas.
- To foster and maintain links that help us achieve our mission.
- To encourage and support research initiatives and disseminate knowledge of research progress.
- To achieve our mission through innovation and influence.
MND Victoria came into existence on October 13, 1981 at a meeting attended by a small group of people with MND and their families, staff of health and welfare groups and other concerned people.
The direction of MND Victoria is controlled by a State Council of twelve members of the Association of whom six must be people with MND, carers, or close associates.
Professional staff are employed for delivery of services to people living with MND, their families, community workers, service providers and health professionals. In conducting the Association's activities and in the provision of services, the staff are assisted by over 100 generous and dedicated volunteers.
MND Victoria has regular contact with similar organisations in other States through the Motor Neurone Disease Association of Australia (MNDA), an umbrella group that serves as a forum for national communication and cooperation. Member organisations participate in a national MND Awareness Week, which is held in May each year.
Through its membership of MND Australia, the Victorian Association participates in an International Alliance of ALS/MND Associations and the global effort to conquer MND.
Read our Annual Review.
Careers at MND Victoria
Find out about Careers at MND Victoria.
The Association is predominantly supported by its own fundraising activities, and in part by grants from the State Government through the Department of Human Services.
In 2016/17, the Association received 20% recurrent funding from the State Government. Other funds are raised through donations, raffles, card sales, bequests, support from service clubs, and from philanthropic trusts and company sponsorship.
We are grateful to the following companies for supporting our work to provide the best possible care, support and VITAL equipment for people living with motor neurone disease:
Find out more about Our History.