Black History Month: Meet Kelly-Ann
“Over a decade ago, I experienced numbness in my legs, and it progressed until I had no feeling in my left foot. I…
Black History Month: Meet Masini
“Throughout history, Black women have faced dangerous stigmas. Some of which have ranged from being aggressive, angry, and ignorant to being strong, confident,…
Global Diversity Awareness Month
The MS community is a global community, made up of individuals from a variety of cultures, ethnicities, and backgrounds. Everyone has their own…
Making the Right Call
Guest post by Frances Bartlett “We get calls from newly diagnosed people and their family members–often, they’re in shock and looking for reassurance,”…
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…
Reprioritizing my life to save it
Guest post by Kate Thompson, MS Bike ambassador That first year I was diagnosed with MS was hard — hard in so many…
Mother hood and MS: Having multiple children and multiple sclerosis
Guest post by Lori, MS Walk ambassador shares her experience with motherhood and MS We had just moved to Calgary in 2004 –…
MS research improves peoples’ quality of life
Guest post by MS Walk ambassador, Darcie opens up about how her neurologist’s foresight saved her quality of life. I like to think that I’m…
