MPS Society Australia is a registered Australian non-profit charity formed by parents, relatives and friends of people diagnosed with mucopolysaccharidosis (MPS) and related diseases. Its purpose is to value, nurture and support affected individuals and families, helping ensure they do not have to face diagnosis and its challenges alone. The organisation builds connections among people with shared experiences, fosters a supportive community, and provides access to trusted information, resources and guidance.

MPS Society Australia offers information about MPS and related conditions, including MPS I, II, III, IV, VI, VII and IX, as well as mucolipidoses ML II and ML III. Its website provides resources for people with MPS, parents, siblings, friends and caregivers, with content tailored to different family members and life stages. The organisation also shares personal stories and information about its work and history. Supporters can contribute through donations, including online card payments or offline donations. Through community support and hope for better treatments and a cure, the Society works toward brighter futures for everyone affected by these rare inherited disorders.