This MS Awareness Month, find the resources you need to thrive with MS Canada. Join a community that supports you on every step of your MS journey. | MS Canada
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This MS Awareness Month, find the resources you need to thrive with MS Canada. Join a community that supports you on every step of your MS journey. | MS Canada
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This May, the Multiple Sclerosis (MS) Society of Canada brings the MS community together for MS Awareness Month with the launch of #WeChallengeMS, a nationwide virtual movement urging people to turn everyday acts into extraordinary actions. Throughout the month, MS communities across the country will connect virtually to rally with the tens of thousands of Canadians affected by MS. More Global News Morning videos can be found here: http://globalnews.ca/halifax/videos/ | Global Halifax
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This May, the Multiple Sclerosis (MS) Society of Canada brings the MS community together for MS Awareness Month with the launch of #WeChallengeMS, a nationwide virtual movement urging people to turn everyday acts into extraordinary actions. Throughout the month, MS communities across the country will connect virtually to rally with the tens of thousands of Canadians affected by MS. More Global News Morning videos can be found here: http://globalnews.ca/halifax/videos/ | Global Halifax
802 viewsApr 30, 2020
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MS Society goes virtual to rally Canadians for MS Awareness Month
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MS Society goes virtual to rally Canadians for MS Awareness Month
Apr 30, 2020
Global News
Burgers to Beat MS celebrates 10 years supporting MS Society of Canada
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Burgers to Beat MS celebrates 10 years supporting MS Society of Canada
Aug 16, 2018
Global News
What’s happening at the MS Society of Canada? Promising research, community connection and more — all because of you. Read more in the 2022 Spring Progress Report. | MS Canada
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What’s happening at the MS Society of Canada? Promising research, community connection and more — all because of you. Read more in the 2022 Spring Progress Report. | MS Canada
148 viewsApr 1, 2022
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2021 Year in Review: The MS Society of Canada is Accelerating Progress in MS Research - Blog - MS Society of Canada
2021 Year in Review: The MS Society of Canada is Accelerating Progress in MS Research - Blog - MS Society of Canada
Dec 2, 2021
mssociety.ca
Help pave the way to a future free of MS! Support thousands of Canadians who live with MS by making a gift during MS Walk on May 29 and you’ll bring us one step closer to a cure. ❤️ | MS Canada
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Help pave the way to a future free of MS! Support thousands of Canadians who live with MS by making a gift during MS Walk on May 29 and you’ll bring us one step closer to a cure. ❤️ | MS Canada
2.4K viewsMay 4, 2022
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Time is running out! Your gift can go 3x as far to fund support services for the MS community and research for a cure. | MS Canada
22.8K viewsNov 23, 2020
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Find the resources you need to thrive with MS Canada. Join a community that supports you on every step of your MS journey. | MS Canada
5.2K views7 months ago
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Finding Strength: One Woman’s MS Journey and the power of community
May 5, 2025
MSNGlobal News
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The Multiple Sclerosis Society of Canada is excited to announce today a $5 million grant in support of the first, international, multicenter clinical trial to investigate cognitive rehabilitation and aerobic exercise in improving cognition in people with progressive multiple sclerosis. The study, led by Dr. Anthony Feinstein (University of Toronto and Sunnybrook Health Sciences Centre) and a group of international MS rehabilitation specialists has the potential to provide a treatment option for
3.8K viewsSep 12, 2018
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The MS Society’s Director, Government Relations and Advocacy, Julie Kelndorfer, testified at a House of Commons committee about the Canada Disability Benefit, a proposed federal benefit that would help lift Canadians with disabilities out of poverty. Watch below as Julie speaks about how important income security is for the MS community. You can watch more of the presentation at bit.ly/3UoIjKn | MS Canada
765 viewsNov 9, 2022
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Take a moment to look back on everything you've made possible in the last 12 months for Canadians living with multiple sclerosis. There were many amazing things that happened in MS research in 2015 -- and it wouldn't have happened without the support of our amazing donors, volunteers and event participants. Thank you! Thank you for your commitment to Canadians living with MS in 2016. #endMS #TeamFight #WhateverItTakes Happy holidays! Everyone at the MS Society of Canada | MS Canada
12 viewsDec 22, 2015
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Across Canada, people living with MS and their loved ones feel alone because they haven’t been able to connect with someone who understands their experience. With your support through the 1:1 Peer Support Program, they no longer need to. Whether you live with MS, or are taking care of someone living with the disease, sign up to “match” with a Canadian looking for support. By sharing your experience with a peer via telephone or internet-based apps, you will help change the life of someone in the
2.1K viewsJun 15, 2020
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Dr. Knox, one of our Hermès Canada| MS Society Wellness Research Innovation Grant recipients, shares with us the research she’s doing to enhance #LifeWithMS. She’s testing an innovative, web-based physiotherapy program that will help people living with MS manage their disease, overcoming the geographic, economic and/or mobility barriers to accessing individualized physiotherapy programs. https://drkarenlee.ca/the-faces-behind-the-research-spotlight-on-wellness-and-ms-part-iii/ | MS Canada
2.3K viewsMay 16, 2017
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WATCH: Dr. Pamela Valentine with the Multiple Sclerosis Society of Canada joins Global News Calgary to explain the link between vitamin D deficiency and MS. | Global Calgary
17.7K viewsNov 17, 2018
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Supporting Those Living with Multiple Sclerosis through MS Walk 2021
8.3K viewsMay 12, 2021
Global Newsfourniernatalie
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Canada is home to one of the strongest MS research communities in the world. We’re committed to keep this momentum going by supporting and funding MS researchers – whether they’re in the early stages of graduate school or conducting research as an independent investigator. Along with Parisa, we’re excited to share more of the up-and-coming researchers who are advancing research across our four impact goals. Thanks to our generous donors, sponsors, and fundraisers, we’ve invested over $218 millio
652 viewsAug 8, 2024
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Canada has the highest rate of multiple sclerosis in the world and MS is one of the most common neurological diseases affecting young adults in Canada. Faced with these facts, Canadians have come together to raise $6.5 million in the first six years of A&W Canada's Cruisin’ to #endMS campaign, which has funded research find a cure and develop treatments to improve quality of life. It has also allowed us to push for better support of caregivers, provide wheelchairs and other special equipment for
23.7K viewsAug 27, 2015
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Many people living with relapsing MS say making treatment decisions can be complicated. Deciding whether you want to treat your MS, or how, can depend on many factors. It’s as individual as you are. Our Treatment Stories is a series of honest accounts from people with MS about how they made that decision. Below is a trailer – watch our full, interactive films here: https://mssoc.uk/2LVDdTa | MS Society UK
65.4K viewsJun 4, 2018
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It can be overwhelming to deal with a new diagnosis of MS. And if you don’t know much about MS, you might be wondering what your diagnosis means. Our short video explains what MS is. But if you’ve got more questions about MS, or just want to talk, our MS Helpline is always here for you. 🧡 Click the link in the comments to find out how to get in touch. | MS Society UK
5.3K views3 months ago
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Living with MS can leave people feeling lonely and isolated. Help us make sure no one has to face MS alone. | MS Society UK
30.9K viewsDec 11, 2018
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People with MS and their loved ones are experts in their condition. So we work together to find solutions to the challenges people living with MS face. When people living with MS are fully involved in every stage of a project, we call this co-production. Find out more, and discover how you can get involved https://mssoc.uk/3hhCnll | MS Society UK
6.4K viewsJul 5, 2021
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Living with MS can leave people feeling isolated. Our MS Helpline and local groups can make all the difference. | MS Society UK
34.3K viewsNov 29, 2018
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Empowering people affected by MS to live their best lives
Apr 22, 2024
nationalmssociety.org
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What is multiple sclerosis (MS)? Many people have a vague idea, but there is still lots of confusion out there. This MS Awareness Week, let’s change that! We created a new animation to explain MS. Please share it far and wide! Here is more info on what MS is: https://mssoc.uk/2Gpunwe | MS Society UK
55.6K viewsApr 25, 2019
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For tens of thousands of people, a diagnosis of progressive MS can mean a future with no available treatments to slow or stop their MS from progressing. But we can change that. Donate now to help drive forward the MS treatment revolution. One donation. Double the Impact | MS Society UK
935 viewsMar 17, 2025
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Every MS letter tells a story. 🎥 MS Letters are the real stories of people affected by MS. They’re about life with MS. The highs and the lows. And the power of our collective commitment to stop MS. 🧡 In the final year of our Stop MS Appeal, we want to raise £100 million to help fund vital research needed to slow or stop MS progression for everyone. 🔬 These letters are real. So is the impact you can make. Donate today: https://mssoc.uk/3Jjt4SV | MS Society UK
4.9K views6 months ago
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Be part of something incredible this spring and join the MS Superstars on one of our Ultra Challenges in 2025. Sign up today and help raise vital funds to help us to stop MS. | MS Society UK
136.7K viewsFeb 28, 2025
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If you're impacted by MS, our online forum is there to support you. 🧡 You can get advice, find support, or just chat to other people who understand MS. Join our free community forum 🔗 https://mssoc.uk/4jpI4e5 | MS Society UK
1.8K views11 months ago
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