Letter from a Caregiver
Dear Dad, I will never forget when you were first diagnosed with multiple sclerosis. It was ten years ago and I was only…
I live with MS, but it’s not who I am.
Guest post by Charlotte McCarthy I want to take you to the beginning when it all began for me, because that is where…
On the persistence of art and friendship
Lelainia has been an artist all her life. In 2007, when she lost feeling in her arms due to damage in her spinal…
An act of recovery: When treatments become triggers
Recovery : Noun /rəˈkəv(ə)rē/ The action or process of regaining possession or control of something stolen or lost. Some people living with multiple…
We challenge you to challenge MS
Here at the MS Society, we host a full suite of fundraising events throughout the year, and across the country. You may have…
Taking action to improve #LifeWithMS
By Benjamin Davis Canada has the highest rate of multiple sclerosis in the world, which is why Canadians needs us – more than…
Women in the changing world: International Women’s Day 2017
Women in Canada are three times more likely to develop MS than men. Women also face significant barriers to finding reliable information about…
Family matters: Tales from a pediatric MS clinic
People in Canada are most commonly diagnosed with MS between the ages of 15-40, but did you know that it can affect children…
It’s time to tell the world: Kiss Goodbye to MS
Kiss Goodbye to MS is the first and only global fundraising and awareness campaign for multiple sclerosis. We talk a lot of talk…
