“We are so blessed that our son is like a best friend to us. We love that he can live with us and enjoy the family life that all kids should experience.”

Cathy, her son Daniel, and other friends and family stand outside for a group picture.

In 1995, when her son Daniel, was diagnosed with Duchenne muscular dystrophy, Cathy Cunningham was thrust into a world that was unfamiliar. Those first few months were hard, especially as a parent, but gratefully her son quickly developed his own set of tricks to overcome the hurdles in his way.

Now at 32 years old, Daniel takes part in everything he can and has a network of support that includes his parents, his two brothers and an array of assistive technology and equipment.

“Muscular Dystrophy Canada has played a big role in our lives over the past 30 years. Not only have they supported our family, but we’ve volunteered, started a local chapter, shared our story, hosted and attended many events and so much more”.

For 28 years, Cathy has been a loyal donor to Muscular Dystrophy Canada. Seeing first-hand the impact her funds have had, Cathy shares, “I’m proud to donate because Muscular Dystrophy Canada provides a support system to help families navigate their own complex journeys. Our family has learned so much about Duchenne muscular dystrophy, but we can’t know everything. When we have questions, Muscular Dystrophy Canada is there. We also know the importance of making sure that research in Canada is well-funded, so advancements can continue to improve and save lives.”

Cathy’s impact over nearly three decades has changed lives and we are so grateful for her, her family, as well as the leadership and support of our many volunteers, partners and donors. Together they continue to break down barriers for the neuromuscular community.


If you would like more information about making a donation, please reach out to Jennifer.Williams@muscle.ca.

“Early diagnosis and effective treatment are critical to achieving the best possible outcomes for babies born with this neuromuscular condition...”

Dr. Pranesh Chakraborty

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