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

Both Jason and Bri-anne have people close to them affected by MS.  They have seen its effects.  They have felt the helplessness of not being about to do more for the people they love.

However, they have also seen a lot of the great work The MS Society of Canada does for those affected by MS.  Not only are they working hard towards finding a cure, they are also committed to assisting those currently living with the disease though local chapters, clinics and information sessions.

With new and exciting research being conducted, this is a time of hope.  Neither Jason nor Bri-anne are doctors. They won’t be making any great scientific breakthroughs.  But the He Walks, She Walks* journey is something they can do.  It is a way to combine their skills and passions towards a common and worthwhile purpose. This is a way to be part of a solution and lend help the people they care about.

We can help end MS.