Enjoying the Journey: How to Plan Your Cycling Route
Picture this: it’s a beautiful day, your bike is all tuned up, your helmet is on and you’re ready to hit the open…
Indigenous People and Multiple Sclerosis
Multiple sclerosis (MS) is a disease that does not discriminate – it can affect anyone at any time, often in the prime of their lives. In…
Faces Behind the Science: Kelsi Smith
Kelsi Smith is a Canadian who is pursuing her PhD in the area of neuroscience and epidemiology at Karolinska Insitutet. In 2020, Kelsi…
New Developments in MS Research from ACTRIMS Forum 2021
The MS Society of Canada is proud to share new developments in multiple sclerosis (MS) research from the 6th annual Americas Committee for…
Dear Richard: A Letter To My Husband
Dear Richard, Five years. I feel like we’ve lived a lifetime in these last five years. It’s crazy to think how little we knew then. I…
Millennials and MS: Christina Andaya
There are questions about being a millennial with MS that you won’t find answered in any Google searches. Like how do you think…
Dear Marc: A Letter to my Husband
Dear Marc, If I had to write this letter shortly after being diagnosed with multiple sclerosis (MS), it would have had a much…
#TakeActionForMS: Lance & the EI Sickness Benefit
“I disclosed my MS diagnosis to my employer almost immediately. I wanted them to know there was a genuine reason why things had…
Slipping Through The Cracks: My Invisible Disease in the Workplace
“I find people have a preconceived notion that if you can work full-time, you surely can’t be that bad. Because multiple sclerosis can be episodic and invisible,…
Lessons From Cyber School: A First-Year Teacher During COVID-19
Most teachers remember their first year in the classroom. For Spencer Davis, a first-year teacher who was diagnosed with MS last year, the…