Multiple sclerosis is a complex disease. While it is most often diagnosed in young adults, aged 15 to 40, we know that it affects children, some as young as two years old. The impact is felt by family, friends and by the community. MS is unpredictable, affecting vision, hearing, memory, balance and mobility. Its effects are physical, emotional, financial, and last a lifetime. There is no cure.

The Multiple Sclerosis Society of Canada is here to help. No one need face MS alone. In communities across Canada, our volunteers and staff provide information, support, educational events and other resources for people with MS and their families. Researchers funded by the MS Society are working to develop new and better treatments. Their ultimate goal is the cure for MS.

Did you know ...

• Canadians have one of the highest rates of multiple sclerosis in the world.
• MS is the most common neurological disease affecting young adults in Canada.
• Every day, three more people in Canada are diagnosed with MS.
• Women are more than three times as likely to develop MS as men.
• MS can cause loss of balance, impaired speech, extreme fatigue, double vision and paralysis.
• MS was first identified and described by a French neurologist, Dr. Jean-Martin Charcot, in 1868.
• We don't know what causes MS but researchers are closer to finding the answer.

Select from the menu items on the left to find out more about multiple sclerosis and life with MS.

Multiple Sclerosis   Living with MS   Research   Treatments   Donate Now   Get Involved    Special Events

Home    About Us    Advocacy    Media    Contact Us    Site Map    Privacy    Français