Category: Multiple Sclerosis Research

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…

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,…

“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…

“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…

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,…

This content is password protected. To view it please enter your password below: Password: The post Protected: The MS Bike 12-Week Training Plan  appeared first on Blog – MS Society of Canada. Source: blog.mssociety.ca

“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…

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…

Multiple sclerosis (MS) can be an unpredictable disease. Living with MS is different for every person and the symptoms and progression of the disease can vary widely for individuals.   Thankfully, technology has come a long way with tools that help managing MS, and life in general, a bit easier. The following apps can help with…

It’s Giving Tuesday If you are fortunate enough to be in a position to contribute to charitable causes, I ask you to consider this organization so close to my heart. 3i Housing of Maine is building a 50 unit, accessible, affordable housing complex in Scarborough, Maine. Please watch the video below, and visit our website….