Wilbur VS MS
“I appreciate mobility. I appreciate being able to remember things. I appreciate being able to walk. Having gone through a period of time…
My mom: the fiercest competitor I know
Guest post by: Christine Sinclair When I was a young girl, I remember my mom started using a cane. I never understood why.…
Letter from a father, living with MS
Dear Amelia, A few months ago, you wrote me a letter – a letter about what it feels like to be my caregiver…
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,”…
Be a part of the change – take action to improve #LifeWithMS
Nearly 100 meetings with parliamentarians. More than 100 hands to shake. Countless personal stories shared. Canada has one of the highest rates…
Sibling Support: How a brother and sister bonded through having MS
Guest post by Kayla Dalley To some, multiple sclerosis could be viewed as a force intended to push you apart from your friends…
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…
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…
