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…
Brief attack, lasting impact
by Robyn Cohen It took me almost a full year to recover after my first MS relapse. As this episode unravelled my life,…
MS hits close to home
Interview with Kate and Sam I recently sat down with two of our #MSBike ambassadors, who happen to both be affected by multiple…
Living with MS as a 20-something, part 1
Amanda, Juan and Lizelle have more than a few things in common: they are all unstoppable forces in this world and they’ve all…
