Canadian MPS Society
Support Team MPS!
The Canadian MPS Society is the only national organization that supports families that are affected with lysosomal storage diseases. These are rare, progressive genetic disorders that affect the patient's heart, respiratory system, bones, joints and central nervous system. Although there are treatments available for some forms of MPS, there is no cure, and most of our MPS members never live to be adults.
The Canadian MPS Society strives to support families who are affected with these diseases, to educate medical professionals and the public about these diseases, and to fund research for a treatment and an eventual 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 judy@mpssociety.ca.
Help make a difference for our kids!!!