Multiple Sclerosis Society of Canada

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 needs to 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.

Help End MS. Give Now.