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Rare Voices Australia

Summary of Support

RVA is committed to advocating in ways we believe are likely to be the most effective and in a manner that is solutions-focused, respectful and continues to build and protect RVA’s ongoing relationships with all stakeholders: policy-makers, Governments, Departments of Health, clinicians, practitioners, researchers, academics, industry as well as people living with a rare disease, and their family and carers.

About Organisation

Rare Voices Australia (RVA) is the national peak body for Australians living with a rare disease. RVA provides a strong, unified voice to advocate for policy as well as health, disability and other systems that work for people living with a rare disease.

Our person-centred focus sees us working with all key stakeholders, including people living with a rare disease, governments, key peak bodies, researchers, clinicians and industry. We advocate for the best outcomes for Australians living with a rare disease.

HeartKids is not affiliated with this support group or organisation. It is the responsibility of the individual and/or their carer(s) to determine whether this or any other organisation on this website may provide some benefit to them.

Last Reviewed: 25 August 2026

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