Q&A: Caregiving during COVID-19
During the rapidly evolving COVID-19 pandemic, loved ones are stepping up to care for and protect the safety of vulnerable populations. For those…
Stories on Women’s Health and MS
Women are 3x more likely to be diagnosed with MS than men. On International Women’s Day, we’re shedding light on some of the challenges faced…
Through thick and thin: Estelle and Adam’s MS love story
Guest post by: Estelle McLellan and Adam Laufer When Estelle and Adam first started dating, they never anticipated to have a third wheel…
Beyond the Stigma
I was diagnosed with MS in 2011. Some people remember the day of their diagnosis like it’s an anniversary. They recall the weather,…
From Denial to Acceptance: A story about Catherine’s journey with MS
“For years, denial kept me from facing my MS head-on. Rather than learning how to live with it, I was ashamed of the…
My MS journey: beyond the lesson plan
Guest post by: Christine Rutherford They tell you that you have MS, but no one tells you how it feels to live with…
Giving Back Through my MS
Living with MS can mean giving up a lot. MS affects each person differently and the symptoms can make a significant impact on…
Jonathan’s MS: a voyage to volunteerism
“I can’t think of a better cause to support than the MS Society of Canada when you’re faced with this disease.” Jonathan Allenger…
A match made in heaven – the story of our 1:1 peer support program
Mari-Lynn has always loved to connect with people. After reluctantly leaving her teaching career because of her multiple sclerosis diagnosis, Mari-Lynn looked for…
