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
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Living with MS can leave people feeling isolated. Our MS Helpline and local groups are there for you. | MS Society UK
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Living with MS can leave people feeling isolated. Our MS Helpline and local groups are there for you. | MS Society UK
34.3K viewsNov 29, 2018
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Living with MS can leave people feeling isolated. Our MS Helpline and local groups are there for you. | MS Society UK
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Living with MS can leave people feeling isolated. Our MS Helpline and local groups are there for you. | MS Society UK
62K viewsDec 12, 2018
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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
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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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These letters are real. So is the impact you can make 🧡 MS Letters shares the intimate words of people affected by MS, like Zoë – conveying what's sometimes too hard to say out loud. Your donation can help turn world-leading research into life-changing treatments. Help us write the end. | MS Society UK
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These letters are real. So is the impact you can make 🧡 MS Letters shares the intimate words of people affected by MS, like Zoë – conveying what's sometimes too hard to say out loud. Your donation can help turn world-leading research into life-changing treatments. Help us write the end. | MS Society UK
311.7K views5 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
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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 viewsDec 6, 2021
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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
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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
33.7K views5 months ago
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Empowering people affected by MS to live their best lives
Apr 23, 2024
nationalmssociety.org
How to volunteer for people with MS
Feb 28, 2019
mssociety.org.uk
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Whether you have MS, or care about someone who does, our community is here for you. | MS Society UK
47.4K viewsDec 24, 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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“The MS Society just felt the natural thing to do, because of my mum’s story, and it could help her live on.” Say hello to Steve 👋 He shares his memories of his mum, who lived with MS, and why the progress of MS research means so much. And why he’s decided to leave us a gift in his will 🧡 Your generous donations are bringing us closer to a future free from MS. Find out more about leaving a gift in your will: https://mssoc.uk/4mOGpQX | MS Society UK
2.6K views7 months ago
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These letters are real. So is the impact you can make 🧡 MS Letters shares the intimate words of people affected by MS, like John – conveying what's sometimes too hard to say out loud. Your donation can help turn world-leading research into life-changing treatments. Help us write the end. | MS Society UK
30.1K views5 months ago
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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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Our MS Society local Councils make sure people affected by MS feel included, seen and heard, wherever they are in the UK. We’re looking for new members to join our Councils in Northern Ireland, Wales and Scotland. Join Catherine and apply now! | MS Society UK
11.8K viewsOct 18, 2021
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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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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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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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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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Are you or anyone you know affected by MS? You’re not alone. Open conversations can make a difference. | MS Society UK
20.9K viewsSep 12, 2016
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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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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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🌟 Important info for anyone with MS on income-related ESA or legacy benefits! 🌟 Are you living with MS and receiving income-related Employment and Support Allowance (ESA) or any other legacy benefits, like housing allowance or income support? If the answer is yes, we've got some important advice for you. ⬇️📽️ Need more support? Read about moving to Universal Credit on our website: https://mssoc.uk/4fz61y5 | MS Society UK
1.8K viewsMar 3, 2025
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Our MS Helpline is closed at the moment. But have you used our forum before? 💻 You can connect with others living with MS, share tips and get advice. Our forum is open to everyone affected by MS. Find out how to register here: https://mssoc.uk/3PF1zTq | MS Society UK
691 views4 months ago
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Need a place to connect with others who are affected by MS? We Talk MS is here for you! Join Donalda and others from our community to share your experiences and chat with people who truly understand the MS journey. Sign up today: bit.ly/3NVg1G1 #WeTalkMS #MultipleSclerosis #MSCommunity | MS Canada
461 viewsNov 14, 2024
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Whether you're feeling lost after receiving a diagnosis of MS, or are frustrated by a symptom you've dealt with for twenty years, we know that having somewhere to turn is so important. Our MS Navigators are trained to point you in the right direction towards resources, both online and in your community, that will meet your specific needs - be it questions about your treatment, questions about a symptom you've been experiencing, or because you're looking for moral support. Reach out to one of our
4K viewsJan 25, 2017
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MS Society goes virtual to rally Canadians for MS Awareness Month
Apr 30, 2020
Global News
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We surveyed more than 2,000 people around the UK to find out what awareness of MS is like. 🎤📝 Only 1 in 5 UK adults know MS is most likely to be diagnosed in people in their 30s and 40s. This isn't good enough. ❌ Multiple sclerosis needs to be better understood, so more people living with MS know that they’re not alone. 🧡 Read about our latest awareness polling on our website: https://mssoc.uk/4i4QA1U | MS Society UK
2.7K viewsMar 5, 2025
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There's strength in solidarity. Join the MS community and improve #LifeWithMS by asking your MP to: Make work, work. Make ends meet. Make access a reality. Make health research a priority. | MS Canada
17.8K viewsSep 1, 2018
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What’s one thing you wish more people understood about living with MS? We put this question to our community and here’s what they said. Do these sound familiar to you? If you’re struggling and need support, our MS forum is here for you. 🧡 You can connect with others and share advice. Go to the link in the comments to find out how to register. | MS Society UK
6.5K views3 months ago
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