Why Not Me?
Guest post by: Lindsay Ireland I believe in the power of perspective. Reframing the narrative in my head may not cure MS, but…
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…
Protected: The MS Bike 12-Week Training Plan
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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,…
World Mental Health Day
Prioritizing Mental Health for MS Management and Overall Well-Being Every year on October 10, the World Health Organization (WHO) recognizes World Mental Health…
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…
It’s that time of year again: back-to-school tips from the MS community
The new school years means new friends, teachers, classrooms, and experiences. It’s normal for anyone to feel anxious, but for students, parents, and…
Meet Five Canadian MS Researchers To Get Excited About
Canadians are known for many things – our hockey teams, maple syrup production, and universal healthcare come to mind – but our MS…
Pride Month: Elevating Voices Within the 2SLGBTQIA+ MS Community
In celebration and recognition of Pride Month, we are featuring stories from the 2SLGBTQIA+ MS community. All people impacted by multiple sclerosis deserve…
Coming Back to Win: Fatherhood and MS
Guest post by: Dale Allen Berg For 20 years, I endured a host of odd, unexplained symptoms. Starting at 15 years old, I…