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An estimated 93,500 Canadians are living with multiple sclerosis (MS) according to the Canadian Community Health Survey. Much is unknown about MS, and Canada is estimated to have one of the highest MS rates in the world.

To further our knowledge of MS, work began on the Canadian Multiple Sclerosis Monitoring System (CMSMS) in April 2011. An extensive network of experts is collaborating on this work. This network includes people living with MS, their caregivers, the Multiple Sclerosis Society of Canada, the Canadian Network of Multiple Sclerosis Clinics, clinicians, researchers, international experts and various governments. Since September 2012, the CMSMS has been ready to receive data.

The CMSMS will

  • Record, measure and monitor the evolution and treatment of MS in Canada
  • Improve the understanding of disease patterns across Canada, variations in treatment and long-term patient outcomes
  • Provide a minimum data set and data standards
  • Provide longitudinal data that is pan-Canadian and comparable across jurisdictions

We welcome your feedback and questions

Information on multiple sclerosis and the CMSMS

 Information for people with MS
 Reports and analyses
 Key resources
 Metadata
 Related content

Information for people with MS

Reports and analyses

Key resources

Metadata

Metadata is information about data. It helps users understand and interpret data from a specific source.

Find out more about CMSMS data: