About the MPS Society

The Australian MPS Society is a non profit organisation formed by parents, relatives and friends of those suffering from a range of rare genetic disorders known collectively as the mucopolysaccharide (or MPS) diseases. 

The MPS Society supports individuals affected with MPS/ML, parents of affected children, other relatives and friends.  As well, we extend our support to those affected by related disorders and invite them to be members also. Professionals working in the MPS and related fields and all those interested in the MPS and related diseases are welcome to join the Society.

The Australian MPS Society is governed by a committed Board of Directors  elected by our membership. We have strong relationships with medical experts who advise us on a range of scientific and policy matters.