Trying to Find Meaning in My MS
Guest post by: Anna Giannakourus One day I was jogging, and I kept tripping over my feet. I was pregnant at the time, and already had a lot…
The Power of Positivity in the Face of Uncertainty
Guest post by: Donalda Martin-Gagnon It was one morning in 2009 when I woke up and I couldn’t move the right side of my body. It almost…
Indigenous Disability Awareness Month: A Conversation with Dr. Rheanna Robinson
The Indigenous population in Canada is a culturally and geographically diverse group that includes First Nations, Métis and Inuit people. According to Statistics…
A Confrontation with Uncertainty: Kajal’s MS Story
Guest post by: Kajal Rai A cure for MS would mean that I could have a life of normality and a life of…
New ventures lead to new found bonds
Guest post by: Carrie MacLean When I was diagnosed with multiple sclerosis (MS), I thought I only had a few years to live.…
Millennials and MS: Abdalla Ahmedin
There are questions about being a millennial with MS that you won’t find answered by a Google search. How do you think about…
Indigenous People and Multiple Sclerosis
Multiple sclerosis (MS) is a disease that does not discriminate – it can affect anyone at any time, often in the prime of their lives. In…
Faces Behind the Science: Kelsi Smith
Kelsi Smith is a Canadian who is pursuing her PhD in the area of neuroscience and epidemiology at Karolinska Insitutet. In 2020, Kelsi…
MS Navigators – pillars of support
A diagnosis of multiple sclerosis (MS) comes with unanswered questions. Your medical team can provide expert advice on halting disease progression and available…
