A huge thank you to the Cape Breton Regional Fire Fighters, Local 2779, for holding their annual Boot Drive on November 1 and raising an incredible $4,000 in just a few hours. This marks one of their most successful drives to date. Since 1977, these dedicated Fire Fighters have

A heartfelt thank you to the Eel River Crossing Fire Fighters for holding their annual #FillTheBoot drive on October 18 and raising $1,733.05 for the neuromuscular community. Since 1989, they have raised an incredible $21,000, helping to #BreakDownBarriers with every donation.

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Tonight marks one of the most meaningful moments of our year. We come together for Muscular Dystrophy Canada’s Dr. David Green Awards Banquet to celebrate the people who power our mission. From volunteers and Fire Fighters to donors, fundraisers, researchers and healthcare

This weekend, Fire Fighters are hosting boot drives to raise critical funds and awareness for Muscular Dystrophy Canada. Come, #FillTheBoot in your area, and help our Fire Fighter partners break down barriers for Canadians affected by #NeuromuscularDisorders. Every dollar raised

Don’t forget! The Hope on the Horizon event for myasthenia gravis is on November 28. In the last year alone, there have been several new targeted treatments for MG. Where are we at with approval and access? What do these new treatments mean for you? Learn the answers to these

The Ottawa Fire Services – Districts 6 & 8 held their first annual First Responders Golf Tournament in support of Muscular Dystrophy Canada this August, raising an astonishing $13,741! Their incredible motivation to raise awareness and funds in this inaugural event was exciting

There are 3 clinical trials for myotonic dystrophy happening right now in Canada and more in the pipeline. Want to know what this means for you? Register for the Hope on the Horizon event happening on November 27, where we will share updated information on the current state and

Join us next week, on November 26, for the Hope on the Horizon event to learn more about the treatments, therapies and clinical trials for Duchenne muscular dystrophy. While the recent approval of vamorolone is promising, we know Canada lags behind other countries when it comes

Reminder! Join Muscular Dystrophy Canada for our FA Together: Learn. Share. Connect. mini-regional conference in Calgary — created for individuals and families living with Friedreich’s Ataxia. Join us in-person on December 8 to: ✅ Learn about the latest research advancements

A big thank you to the Deer Lake Fire Fighters for holding their annual #FillTheBoot drive on September 27 and raising $1,536 for Muscular Dystrophy Canada. Since 1978, these committed Fire Fighters have raised $28,700, helping to fund vital research, programs, and services for

Imagine being told you have to try, and fail, a drug that was never approved for your condition before getting access to one that actually works. That’s the reality of many Canadians with Myasthenia Gravis. In a new @HealthyDebate op-ed, Muscular Dystrophy Canada’s Stacey

Thank you to the Dalhousie Fire Fighters for hosting their annual #FillTheBoot drive on September 27 and raising $5,000 in just a few hours, their best year yet. Since 1989, the Dalhousie Fire Fighters have raised over $28,400 to #BreakDownBarriers for the neuromuscular

This weekend, Fire Fighters are hosting boot drives to raise critical funds and awareness for Muscular Dystrophy Canada. Come #FillTheBoot in your area, and help our Fire Fighter partners make a difference for Canadians affected by #NeuromuscularDisorders. 🔗

A huge thank you to the Clarenville Fire Fighters for hosting a successful #FillTheBoot drive on September 25 and raising an incredible $6,700 in support of Muscular Dystrophy Canada. This milestone pushed their total fundraising to over $205,000 since 1977. Your continued

A huge shoutout to the Fredericton Fire Fighters, Local 1053, for hosting their annual golf tournament on July 3 in support of Muscular Dystrophy Canada. Despite the heat and unpredictable weather, they raised an incredible $10,000 for the neuromuscular community. Since 1969, the

From laughter-filled campfires to moments of quiet connection, our Caregiver and Family Retreats remind us what community truly means. This year, at six incredible events held across Canada, we welcomed families and caregivers for weekends of rest, relaxation, fun, and

When Michel was diagnosed with myotonic dystrophy (DM1), his neurologist told him one thing: “Stay strong. Stay active.” Michel took that advice to heart. Under medical supervision, he ran a full marathon — showing his children that even with DM1, there are “no limitations,

Today, we pay tribute to the veterans who bravely fought for us, and thank our fellow Canadians who continue to serve our nation. #RemembranceDay2025

Muscular Dystrophy Canada is thrilled to be hosting two mini-regional conferences next month. Join us in-person in Calgary and Toronto, to: ✅ Hear research and clinical trial updates from experts in Canada ✅ Learn about multidisciplinary care for SMA and FA ✅ Share your lived

This weekend, Fire Fighters in Ontario are hosting boot drives to raise critical funds and awareness for Muscular Dystrophy Canada. Come, #FillTheBoot in your area, and help our Fire Fighter partners break down barriers for Canadians affected by #NeuromuscularDisorders. Every