Support for families. Research for a cure.
Our support and education programs assist those affected in managing the diagnosis and progression of these rare, often devastating, disorders. Funds raised through donations and special events help fund research that provides hope for a brighter future for all children born with lysosomal diseases.
Newly Diagnosed
Have you or a family member recently been diagnosed with MPS or a related disease? We are here to help and can provide you with information and support to help you through this journey.
Become a Member
Becoming a member of the Canadian MPS Society is the beginning of a rewarding relationship between families, associates, and professional. The MPS Community is an incredibly supportive group of families and loved ones working towards finding hope and cures for rare diseases.
Learn About MPS
Mucopolysaccharidoses (MPS) and related diseases are genetic lysosomal storage diseases (LSD) caused by the body’s inability to produce specific enzymes.
2017 Family Conference
Latest News
Check out the latest news here about MPS and related diseases. You can also subscribe to our newsletter so that you will never miss an important update.
Our Stories
Here is a collection of stories and videos from people who have generously shared their experiences of living with MPS. Would you like to share you own experience? Contact us for more information.
Current News and Events
Symptoms of MPS I – Animated Video
Click to watch the video describing early symptoms of MPS I. https://youtu.be/h111oEHS7-c
MPS I Parents talk about their diagnostic journey
Click to watch the video of Canadian MPS I parents where they share their stories about the diagnostic journey of their children. https://youtu.be/tKflBtR6iYI