Want to learn more about #MS, treatment options, and symptom management while connecting with other community members in a supportive and welcoming space?
Join our next online MS 101 – Newly Diagnosed session on June 16 at 6PM ET.
Register today: https://t.co/i9zI0L5ldj
And just like that, #MSAwarenessMonth came and went, but the momentum, support, and connections made throughout May will have a lasting impact.
Thank you for making this month unforgettable and for standing with the #MS community all year round!
Thank you to everyone who joined us for #TheMay50K challenge, moved 50 km (or more!), and supported the #MS community throughout the month. ❤️
Together, we’re one step closer to a world free of MS.
#MultipleSclerosis
The parliamentary e-petition calling on the federal government to modernize the Disability Tax Credit (DTC) closes on June 4.
Sign the petition today and help make sure the DTC better reflects the daily realities of Canadians living with #MS: https://t.co/UJKAASNua6
Yesterday, more than 12,000 people across the country took action, created impact, and showed up in support of the #MS community.
Thank you to every participant, volunteer, donor, and sponsor for making this year’s #MSWalk so special. We can’t wait to see you next year!
MS Walk Day is here! 🎉
Across the country, thousands of people are coming together to raise awareness for Canadians living with #MS and their families.
Every participant, volunteer, and supporter brings us closer to a world free of MS ❤️.
#MSWalk#MultipleSclerosis
Today is #WorldMSDay, a day of solidarity, collective action, and hope.
Almost 3 million people live with #MS worldwide and today, the global MS community is coming together to spread awareness and show support for everyone affected by the disease.
“MS Bike is about more than just cycling—it’s my way of honouring my mom and keeping her spirit alive.” - Craig, MS Bike participant, mom lived with MS
Head to our blog to see how Craig is turning his mom’s legacy into action: https://t.co/PKVv52x1xy
#MSBike#MultipleSclerosis
Molly was diagnosed with #MS when she was 27. She was newly married, had just bought a house, and was suddenly faced with a life-changing diagnosis.
Watch and listen as Molly shares what living with MS has taught her and what she wishes more Canadians knew about the disease.
“My favourite part of MS Walk is being surrounded by others who understand what it’s like to live with MS, that sense of connection is everything.” – Tina, diagnosed in 2019
Join #MSWalk on May 31 and help make sure no one faces MS alone: https://t.co/lWCTEtVSHW
The e-petition calls on the federal government to modernize the DTC to better reflect the daily realities and fluctuating symptoms experienced by people living with #MS.
#TakeActionForMS and sign the petition today: https://t.co/UJKAASNua6
The Disability Tax Credit (DTC) is failing Canadians living with #MS.
Barb, who’s been living with MS for more than a decade, knows this all too well. She started a Parliamentary e-petition, giving us a real chance to change the DTC system for Canadians living with MS.
Join us at our next Hear From the Experts webinar, MS Rehabilitation, where Dr. Sarah Donkers will talk about practical ways to support rehabilitation for people living with #MS.
Tune in on May 20 at 6PM ET. Register today: https://t.co/wijF5IlaBf
Thank you to everyone who joined us and to our community members for sending letters to your Members of Parliament and taking part in our Digital Carnation Pinning in support of #MSAwarenessMonth.
#TakeActionForMS
Last week, our MS Canada team and volunteers were on Parliament Hill for our annual Day on the Hill event, where we had over 60 meetings with federal leaders to raise awareness about life with #MS.
Want to learn more about #MS, treatment options, and symptom management while connecting with other community members in a supportive and welcoming space?
Join our next online MS 101 – Newly Diagnosed session on May 19 at 6PM ET.
Register today: https://t.co/lTTyFOZnmF
It was a pleasure to join the @MSCanOfficial Parliamentary Reception, on behalf of Parliamentary Secretary @mckelvieAJAX. May is Multiple Sclerosis Awareness Month and it's an opportunity to raise awareness and support Canadians affected by MS.