We are dedicated to supporting short-statured Australians and their families through advocacy, education, and fostering a strong, inclusive community.
Providing a safe, welcoming network for individuals with dwarfism and their families to connect, share experiences, and build lifelong friendships.
Working to remove societal barriers, combat discrimination, and promote accessibility and equal opportunities across Australia.
Breaking down stigmas through public education campaigns, medical resources, and school outreach programs.
Dwarfism Awareness Australia was founded on the belief that everyone deserves to live in a society that embraces physical diversity without prejudice.
There are over 400 distinct medical conditions that cause dwarfism, with Achondroplasia being the most common. We strive to provide accurate, up-to-date medical information for new parents, while simultaneously advocating for the social model of disability—ensuring the world adapts to include us, rather than the other way around.
Language matters: We encourage the use of terms like "person with dwarfism," "short-statured," or simply calling someone by their name. Awareness starts with respect.
Access Our ResourcesYour support allows us to fund national community events, create educational resources for schools, and continue our advocacy work across Australia.