The federal government’s 2026 budget left #MS out of the new streamlined application process for the Disability Tax Credit (DTC). We’ll keep urging the government to include MS in the upcoming Spring Economic Update. Sign up for our advocacy updates: bit.ly/4AiELOD
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Our incredible #MSBike community raised $4.79M to fuel critical research and support programs for Canadians living with #MS and their families. Thank you! ♥️
Register for a 2027 MS Bike event today: bit.ly/4sAVXMF
Register for a 2027 MS Bike event today: bit.ly/4sAVXMF
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You can help create a brighter future for Canadians affected by #MS through #WorkplaceGiving.
HealthPartners makes it easy for employees to support health charities and causes they care about through payroll donations.
Learn more at healthpartners.ca
HealthPartners makes it easy for employees to support health charities and causes they care about through payroll donations.
Learn more at healthpartners.ca
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For people living with #MS, some of the most difficult symptoms can often be invisible.
This #InvisibleDisabilitiesWeek, let’s remember that what someone is experiencing on the inside isn’t always visible from the outside. ♥️
This #InvisibleDisabilitiesWeek, let’s remember that what someone is experiencing on the inside isn’t always visible from the outside. ♥️
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Turn your favourite sport into a fundraiser to help end #MS. Register in less than a minute and get the resources and support to get started: bit.ly/4sbZHDQ
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In one week, thousands of people around the world will gather online to attend this year’s @ECTRIMS Patient Community Day, a free global event that brings the latest #MSResearch to the people it impacts most.
Register today: bit.ly/44elQGb
Register today: bit.ly/44elQGb
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October 16 is the last day to take action and urge the Minister of Finance and National Revenue and the Minister of Jobs and Families to include #MS in the new streamlined Disability Tax Credit (DTC) application process. Send a pre-written letter today: bit.ly/3Up4Dc8
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Have questions about #MS or looking for reliable information and support?
Join our next online MS 101 - Newly Diagnosed session on October 20 at 6PM ET to learn more about MS, treatment options, symptom management, and available support.
Register today: bit.ly/4hKsdcr
Join our next online MS 101 - Newly Diagnosed session on October 20 at 6PM ET to learn more about MS, treatment options, symptom management, and available support.
Register today: bit.ly/4hKsdcr
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Excited about your Halloween plans? Turn them into a fundraiser to help end #MS. Swipe to see how we can help you bring your idea to life.
Register in less than a minute. Turn your upcoming spooky event into an MS fundraiser: bit.ly/3TKCegv
Register in less than a minute. Turn your upcoming spooky event into an MS fundraiser: bit.ly/3TKCegv
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Your next get-together could help end #MS. Check out these ideas for fun and easy fall fundraisers. Register in less than a minute to make an impact: bit.ly/4rS0R7m
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Canada’s Drug Agency is reviewing Ocrevus for children and youth 10+ with relapsing-remitting #MS, and families like Erica’s deserve to be part of the conversation. Help shape access to pediatric MS treatments. Share your feedback by October 16: bit.ly/3VyCakq
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In case you missed it: @ECTRIMS Patient Community Day is on October 23. This free global event brings the latest research directly to people affected by #MS and related neurological diseases.
Join online or in-person in Toronto. Learn more: bit.ly/44elQGb
Join online or in-person in Toronto. Learn more: bit.ly/44elQGb
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A Canada-wide survey we funded found that the #MS community may be more diverse than previous research has shown: bit.ly/3TExAR8
Building stronger community partnerships and involving people with diverse lived experiences is important when developing future studies.
Building stronger community partnerships and involving people with diverse lived experiences is important when developing future studies.
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We’re asking for #MS to be included on the list of long-term medical conditions in the new Disability Tax Credit (DTC) application process.
Share this post and send a pre-written letter to federal Ministers urging them to include MS: bit.ly/4zAS10L
Share this post and send a pre-written letter to federal Ministers urging them to include MS: bit.ly/4zAS10L
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A whole lot of Teen Burgers™… an even bigger impact! 🍔
Canadians showed up in a BIG way for #BurgersToBeatMS this summer, coming together to raise $1.56M for the MS community!
Thank you for making a difference for Canadians living with MS and their families. ❤️
Canadians showed up in a BIG way for #BurgersToBeatMS this summer, coming together to raise $1.56M for the MS community!
Thank you for making a difference for Canadians living with MS and their families. ❤️
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Families of children and youth living with #MS should have a say in treatment decisions. Canada's Drug Agency is reviewing Ocrevus for children and youth 10+. Your feedback will help us share what matters most to the youth MS community. Add your voice: bit.ly/4xFYmWY
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Only one week left to apply to our Annual Research Competition! Learn more about our available funding opportunities: bit.ly/4zKCFrd
Apply by October 1 at 4:00 PM ET.
#MultipleSclerosis #MS #MSResearch
Apply by October 1 at 4:00 PM ET.
#MultipleSclerosis #MS #MSResearch
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We’re one month away from @ECTRIMS Patient Community Day, where leading experts will break down the latest research into real-life insights for people affected by #MS and related neurological diseases.
Join online or in-person in Toronto on October 23: bit.ly/44elQGb
Join online or in-person in Toronto on October 23: bit.ly/44elQGb
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Join us for our next Hear From the Experts webinar, Adapting to Change – Acceptance and Resilience, where we'll explore how people adjust to major life changes while building resilience and finding new meaning and purpose.
📆 Tomorrow at 6PM ET
Register: bit.ly/4xBTL8q
📆 Tomorrow at 6PM ET
Register: bit.ly/4xBTL8q
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