Making a difference in MS research
This summer was a memorable one for MS research. In June, we saw the results of the Canadian Bone Marrow Transplantation trial, which…
“MS changed our families. Now we’re going to end MS”
Nearly 100,000 Canadians live with MS, but it also affects the children of those who live with the disease. A generation of young people…
Meet the original members of #TeamFight
Throughout history, women have fought for rights, freedom and power. We are fighters, and we know how to take action to effect change…
Coping with cognitive changes
For some people, multiple sclerosis is an invisible illness. Cognitive impairments such as short-term memory loss, difficulty concentrating and altered moods can have…
Your MS winter safety toolkit
By Sylvia Leonard The cold season can make daily life especially challenging for people living with a disability. Weather-related limitations can present barriers…
Working in partnership to offer caregiver webinars
Over the years I have worked for a number of different health charities. All do great work to provide supports and services and…
World MS Trend Day
Kayla Chatkiewicz has a goal: make #CureMS trend on social media tomorrow. As the creator of the Stop Drop Selfie for MS social…
Adapting your sartorial choices: Dressing for MS
“Vain trifles as they seem, clothes have, they say, more important offices than to merely keep us warm. They change our view of…
One phone call – a life changed forever.
Listen to the clip above to hear Allie’s reaction to the news of her scholarship. I’m excited to announce that Allie Sherwin, whose…
Sometimes, it’s not MS: My journey with neuromyelitis optica
by Lelainia Lloyd, guest blogger You may have heard the acronym “NMO” floating around the MS community and wondered what it means. NMO…