Putting your oxygen mask on first: motherhood and MS
Multiple Sclerosis Society of Canada Blog
by Gabriella Montesano
3M ago
Women in Canada are three times more likely to develop multiple sclerosis (MS) than men. Caregiver and caretaker roles remain predominantly occupied by women, which can lead many women to put the healthcare concerns of others – parents, children, and loved ones – ahead of their own. When it comes to MS, which can require a regular self-care practice, routine medical appointments, and an ongoing treatment regimen, these social and familial expectations can become dangerous for women affected by the disease. The demands of motherhood require women to constantly be vigilant of their children’s ne ..read more
Visit website
The whole picture: A holistic approach to managing MS
Multiple Sclerosis Society of Canada Blog
by Gabriella Montesano
5M ago
Our bodies are made up of systems, no different than the eco-systems making up our planet. Our musculoskeletal, digestive, central nervous, and endocrine systems – to name only a few – each require a specific set of environmental factors to function optimally. A healthy, nutrient-rich diet has the power to optimize the efficiency of each individual system, allowing the entire body to work together to the best of its ability. This is called holistic health, a concept defined by the treatment of your person as a whole, including mental, emotional, and – for some people – spiritual health, rather ..read more
Visit website
Research Highlights from ACTRIMS Forum 2023
MS Society of Canada
by Krystle Forget
1y ago
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 areas of multiple sclerosis (MS) research. Canadian-based researchers and trainees showcased their cutting-edge MS research throughout the forum, representing 24% of the speakers. Dr. Ruth Ann Marrie, neurologist and researcher at the University of ..read more
Visit website
Why Not Me?
Multiple Sclerosis Society of Canada Blog
by Krystle Forget
1y ago
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, it was a scary time. As an adolescent I underwent many surgeries related to ulcerative colitis and have lived with an ileostomy* since I was 11 years old. I understood scary times. Also, I learned some useful coping skills at a young age.  The ostomy surgery s ..read more
Visit website
Black History Month – Meet Luidjy
Multiple Sclerosis Society of Canada Blog
by Krystle Forget
1y ago
“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 hold a pencil and eat again, among other things.  Shortly after receiving my diagnosis, I told myself I had two choices: accept the disease and live with it or live unhappily. As soon as I got out of the hospital, I decided I was going to appreciate everything around me more. I got involved with MS Canada including MS Walk in Terrebo ..read more
Visit website
Black History Month: Meet Kelly-Ann
Multiple Sclerosis Society of Canada Blog
by Gabriella Montesano
1y ago
“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 my brain was working overtime. What does living with MS look like?   I struggled with my initial diagnosis but when I came to the realization that my MS was manageable, I was able to move forward. When given an MS diagnosis, it is the perfect time to allow ourselves to be humble and open to receiving ..read more
Visit website
Protected: The MS Bike 12-Week Training Plan 
Multiple Sclerosis Society of Canada Blog
by Hassan Khan
1y ago
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 ..read more
Visit website
Black History Month: Meet Masini
Multiple Sclerosis Society of Canada Blog
by Krystle Forget
1y ago
“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 to have such an attitude.’ And of course, ‘You are such a strong Black woman. You can handle anything.’ Without really understanding that these phrases are forms of microaggressions, I took some of them as compliments and wore them like a badge of honour. Sayi ..read more
Visit website
2022 MS Research Year in Review: Working Together Towards a World Free of MS
Multiple Sclerosis Society of Canada Blog
by Krystle Forget
1y ago
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 the most promising MS research. In the 2022-23 Annual Research Competition, the MS Society announced over $3.5 million in funding to support MS research in a number of critical and unmet areas, such as understanding and halting MS disease progression, identi ..read more
Visit website
Wellness Apps to Help Manage Your MS 
Multiple Sclerosis Society of Canada Blog
by Gabriella Montesano
1y ago
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 the day-to-day tracking of symptoms, treatments, medications, organizing tasks and notes, and keeping you looped in on the latest news, advancements, and information.   Aby   For iOS and Android  Start a personalized journal to hel ..read more
Visit website

Follow Multiple Sclerosis Society of Canada Blog on FeedSpot

Continue with Google
Continue with Apple
OR