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
FacebookGlobal Halifax
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
Happy National Volunteer Week! It’s that time of year where we celebrate all the hard work our volunteers put in for the MS Society! As an integral part of our organization, volunteers have an immeasurable impact on what we do and help us improve the lives of Canadians living with MS. Kicking things off for #NVW2019, here is our President and CEO, Pam Valentine, sharing her heartfelt appreciation for the many #ActsofGreatness that our volunteers do everyday. "Hi I'm Pam Valentine, I'm the Presid
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Happy National Volunteer Week! It’s that time of year where we celebrate all the hard work our volunteers put in for the MS Society! As an integral part of our organization, volunteers have an immeasurable impact on what we do and help us improve the lives of Canadians living with MS. Kicking things off for #NVW2019, here is our President and CEO, Pam Valentine, sharing her heartfelt appreciation for the many #ActsofGreatness that our volunteers do everyday. "Hi I'm Pam Valentine, I'm the Presid
2.3K viewsApr 8, 2019
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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
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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
For people living with multiple sclerosis (MS), every moment counts. You can help more Canadians get the early detection, diagnosis and treatment they need to stop MS in its tracks. | MS Canada
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For people living with multiple sclerosis (MS), every moment counts. You can help more Canadians get the early detection, diagnosis and treatment they need to stop MS in its tracks. | MS Canada
11.5K views5 months ago
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Finding Strength: One Woman’s MS Journey and the power of community
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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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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
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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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Support Canadian Creators Fighting to End MS. | MS Canada
107.7K views6 months ago
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In 2021, one community made up of tens of thousands of Canadians will walk forward together to show that no person living with multiple sclerosis is alone 🚶‍♀️🚶. Register for MS Walk today as we walk toward a world free of MS: https://bit.ly/38pPFaG. | MS Canada
4K viewsMar 9, 2021
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MS Society calls on government to implement disability benefit
2.5K viewsMay 27, 2022
YouTubeCityNews
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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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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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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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Empowering people affected by MS to live their best lives
Apr 23, 2024
nationalmssociety.org
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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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Multiple sclerosis can be painful, relentless and exhausting. And for many people living with it, there’s nothing to stop their condition getting worse. That’s why we won't stop until we've found treatments for everyone. Will you help transform lives this Christmas by donating to help stop MS? | MS Society UK
168.2K viewsNov 16, 2021
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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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Help us give more than hope to people living with MS. Donate now to fund MS research for new treatments: http://mssoc.uk/2h3VtKa | MS Society UK
21.7K viewsDec 15, 2016
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Sasha has found some peace of mind - there's a treatment for her multiple sclerosis. But too many people still have nothing to stop their condition getting worse. Will you help find the next life-changing treatment and stop MS? | MS Society UK
13.3K viewsNov 8, 2021
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