Your support has improved outcomes for thousands of Canadians, like Ben

“We thought our child was going to die a very slow and painful death. Our world ended, and we were never going back to life as we knew it.” Those were Amanda and Brodie’s first thoughts when they learned their son, Ben, was affected by Duchenne muscular dystrophy (DMD).

For the first three years of Ben’s life, countless doctors and physiotherapists told his parents that he suffered from low muscle tone. Unable to crawl, or walk unassisted, Ben was referred for blood tests. “When the doctor told me he had muscular dystrophy, she sent me information that told me I should expect my son to be in a wheelchair by age six, on a ventilator by age eight and dead by 19,” Amanda says. “It was horrific, devastating news.”

When a Canadian is diagnosed with a neuromuscular disorder, Muscular Dystrophy Canada (MDC) knows they will need a lot of support and have many questions. Your gift today will give families hope. When you’re facing a life-changing diagnosis for your child or family member, hope can make a huge difference.

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Since our inception, MDC has been a leader in funding ground-breaking research for all neuromuscular disorders. For decades, MDC has been helping to accelerate the development of more treatments, therapies, and hopefully, one day soon, potential cures. It is an exciting time for neuromuscular research and we are proud to see incredible advancements that are having real-world impacts on families like Amanda and Brodie’s.

After the initial shock of Ben’s diagnosis wore off, and Amanda and Brodie were able to digest the information they had received, they were referred to MDC by their healthcare provider. Armed with new information about therapies and medication available, Brodie and Amanda started to have hope once again. “I remember feeling that finally there was a light at the end of the tunnel”.

By donating today, you are investing in families like Brodie and Amanda’s. Whether through research investments or helping them navigate upcoming treatments for Ben, your gift can enable so much. Thanks to you and others like you, we can continue to invest in Canadians affected by neuromuscular disorders in the ways that matter most to them.

“The funding that MDC has provided to neuromuscular research has changed our lives infinitely,” Brodie says. “We have seen directly, even from the information we received initially, how far medicine and therapies have come in as little as 10 years. Ben has great doctors who are pushing the envelope to find the next thing – a treatment, therapy or cure. The funding from MDC specifically enables them to do that research and take those chances.”

Being diagnosed with a neuromuscular disorder is very difficult and often shocking. Your mind races between practical concerns and anxious thoughts: what treatments are available? What will happen to me in the next five or 10 years? Who can give me the answers I can trust? By donating to MDC today, you are ensuring families have the answers they desperately require, ensuring hope in the months and years to come. You can help provide clarity and comfort to a family during that difficult time.

Your gift today will ensure that families have access to the most up-to-date information they need when they need it most.

Thanks to improvements in neuromuscular treatments and therapies, today, Ben is an active six-year-old who is able to walk, run and climb. And while Amanda and Brodie are still concerned with what the future holds, they know that Duchenne is a very different disease now, compared to 20 years ago. “Ben has a very serious disease and kids still die from it, but Duchenne is not the disease it used to be. DMD comes in all shapes and sizes, which is thanks, in large part, to how far medicine has come. It is a heavy load to carry, but it would be a lot heavier without the support of MDC.”

Your generosity today will help support MDC’s programs and services, while also investing in critical neuromuscular research. Together, we can provide hope, change the face of muscular dystrophy and other neuromuscular disorders, and improve the outcomes now and for future generations. But we cannot continue this important work without your support.

“Understanding the support that MDC provides to Canadians is huge,” Brodie says. “There is a group of people – the MDC village, that are working day and night on behalf of my family. It affects our day-to-day life and I only see some of it – there is so much work happening beyond the support they provide to our family.”

Please consider making a gift today that will help countless Canadians right now. You can change the future and give hope to future generations.

Donate now!

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