The Grant Family Foundation was founded from a deeply personal journey and a simple belief: every family deserves hope.

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After our son Benjamin was diagnosed with Duchenne Muscular Dystrophy, our lives changed forever. Like so many families facing a neuromuscular diagnosis, we quickly learned that while remarkable progress is being made in medical research, there is still much work to be done.

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Rather than accept the status quo, we chose to take action.

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The Grant Family Foundation was created to raise funds for innovative neuromuscular research, support groundbreaking scientific discoveries, and help accelerate the development of treatments that can improve—and ultimately save—the lives of children and adults living with neuromuscular diseases.

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We believe that meaningful change happens when communities come together. Through fundraising events, corporate partnerships, and the generosity of donors, we are committed to investing in research that brings hope to families today while helping build a healthier future for generations to come.

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Our vision extends beyond fundraising. We aim to inspire others to get involved, raise awareness about neuromuscular diseases, and create opportunities for collaboration between researchers, healthcare professionals, businesses, and communities.

Every dollar raised is an investment in innovation, discovery, and hope.

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Together, we can help move research forward and create a future where every child has the opportunity to live a healthier, stronger life.