The Canadian MPS Society is the only national organization that supports families affected with all types of MPS & related lysosomal storage diseases. These are rare, progressive genetic disorders that affect the patients' hearts, respiratory systems, bones, joints and central nervous systems. Although there are treatments available for some forms of MPS, there is no cure, and many of our members never live to be adults.
The Canadian MPS Society strives to support affected families, to increase professional and public awareness, and to fund research for a cure. To find out more about our organization and our members, please visit our web site at www.mpssociety.ca.
Join Team MPS for a minimum donation of $50.00. We'll cover your registration fee and provide a team shirt. If you have any questions, contact Judy Byrne, Chairperson, at firstname.lastname@example.org.
Help create brighter futures for kids with MPS & related diseases!!!