The journey to end MS
Guest post by Ahmed Nassrat, I Challenge MS ambassador “Show of hands – who here knows someone affected by MS?” All around me, hands…
MS Awareness VS stigma: Vanquishing the taboo
Guest post by Chisani Doyle-Wood, MS Bike ambassador & MS awareness champion On a summer day last year, I was sitting in my…
Where there’s a will, there’s a way
Guest post by Patrycia Rzechowka, MS Bike Ambassador Its been five years since I was diagnosed with MS, and five years since my…
Reprioritizing my life to save it
Guest post by Kate Thompson, MS Bike ambassador That first year I was diagnosed with MS was hard — hard in so many…
Mother hood and MS: Having multiple children and multiple sclerosis
Guest post by Lori, MS Walk ambassador shares her experience with motherhood and MS We had just moved to Calgary in 2004 –…
MS research improves peoples’ quality of life
Guest post by MS Walk ambassador, Darcie opens up about how her neurologist’s foresight saved her quality of life. I like to think that I’m…
Secure your own oxygen mask first: Living with MS
Guest post by Samara Bleiwas, who says living with MS means learning to secure your own oxygen mask first. I’m a mom, wife, business…
Taking a walk in my own shoes
Guest post by Lisa Mackintosh The road to my diagnosis started when I saw my family doctor in October of 2014 because I…
Slow and steady wins the race
Guest post by Kim Cormack I used to love running – I’d run ten laps of Bob Daily stadium almost daily. Now, writing…
An important milestone in MS research and hope for people living with progressive MS
Guest post by Cory Turner – member of the MS Scientific Research Foundation Board We don’t get to pick when we’re diagnosed with…