Treating MS as a piece of luggage
Guest post by: Kelly-Ann Jones When I went to the doctor over a decade ago with a sore back, he automatically sent me…
Protected: MS Read-a-Thon Book List: Stories of Disability and Inclusion
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Doing my part to help achieve a world free from MS
Guest post by: John Duffy My sister, Joanne, was never much of an athlete. She was a bit clumsy. Our parents had a chalet in Craigleith and…
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…
