Symptoms of Multiple Sclerosis Multiple Sclerosis (MS) is a chronic autoimmune disease that affects the central nervous system. The symptoms of MS vary widely and depend on the location of the damage within the nervous system. Some common symptoms include fatigue, numbness or tingling in the limbs, muscle weakness, blurred vision, difficulty with balance and…
Marrakesh: when attitude outweighs infrastructure
A fairly impulsive holiday to Marrakesh this spring, when I was just craving some heat and sun (and easyJet obviously sensed the vibe and launched sales). I didn’t expect an old African city to be super accessible, but it had got to the point where I thought sitting in a street at 30° was preferable…
Research Highlights from ACTRIMS Forum 2023
On February 23-25, 2023, the eighth annual Americas Committee for Treatment and Research in Multiple Sclerosis (ACTRIMS) forum took place in San Diego, California with the theme – MS: Going Viral. This was one of the largest ACTRIMS meetings to-date with over 1,800 participants in attendance, and over 50 presentations and 460 posters across various…
Why Not Me?
Guest post by: Lindsay Ireland I believe in the power of perspective. Reframing the narrative in my head may not cure MS, but it has helped me live my best life. Living with three autoimmune diseases, this outlook has proven its value to me many times. When I was diagnosed with relapsing-remitting MS in 2001,…
Black History Month – Meet Luidjy
“I cried a lot when I was diagnosed. I was 22 years old, and I thought my life was over. I went to the hospital after losing feeling in my right arm. While I was there, I lost feeling in my right side, from my shoulder to my hip. I had to learn how to…
Black History Month: Meet Kelly-Ann
“Over a decade ago, I experienced numbness in my legs, and it progressed until I had no feeling in my left foot. I remember my neurologist talking about MS while I stared at the Parkinson’s poster that was plastered on the wall behind him. I have MS? I tried to keep a straight face, but…
Hi again social services
It must be that enough time had passed since I was last battling social services, that I found the confidence to think moving would be okay… After all, it’s a bungalow, it’s in the same town, just a few small alterations needed. Unfortunately, though, I think unless you’re in an accessible council house and unemployed,…
Protected: The MS Bike 12-Week Training Plan
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Black History Month: Meet Masini
“Throughout history, Black women have faced dangerous stigmas. Some of which have ranged from being aggressive, angry, and ignorant to being strong, confident, and loud. Being a plus-size Black woman, many of these stigmas have followed me throughout my life. I’m used to hearing things like, ‘Masini, you are so funny!’ or ‘You don’t have…
2022 MS Research Year in Review: Working Together Towards a World Free of MS
Looking back at this past year in research, we reflect on key advances that are accelerating our understanding of multiple sclerosis (MS) and the promising research that the MS Society of Canada funds. With the support of event participants, fundraisers, donors, and everyone else in the MS community, the MS Society of Canada can fund…