<div>Help Keep Dylan Moving: Support His Fight Against Duchenne Muscular Dystrophy
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<div>Our 15-year-old son, Dylan is living  with a rare, devastating  and life limiting disease called Duchenne Muscular Dystrophy (DMD). This progressive muscle-wasting disease has already taken a significant toll on his body, limiting his mobility and impacting his quality of life.
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<div>Despite the challenges, Dylan remains brave, resilient, and full of hope. Recently, we discovered a promising treatment available in the United States that may help preserve his mobility and slow the progression of this cruel disease. It offers a lifeline—not just for his body, but for his future.
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<div>However, this treatment comes at a very high cost. As parents, we are doing everything in our power to fund Dylan’s treatment but we simply cannot cover the full expense alone.
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<div>We are reaching out to our community, friends, and kind-hearted supporters to ask for your help. Any contribution—no matter how small—will go directly toward Dylan’s treatment and care.
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<div>Please help us give Dylan the best chance to keep moving, to keep dreaming, and to keep living a full life.
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<div>Thank you from the bottom of our hearts for your support.
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<div>Greg, Terri and Dylan.
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bernard brogan

James Kelly

Rene Pierce

Pauline Greene

Anonymous

Paul Kavanagh

Alan Raftery

Liam Quinn

Tony Mc Guigan

Marzena Chmiel-McDonnell

Conor McMorrow

Petergeard Mcgarrity

Shane Heraty

Dermot Crowe

Dylan's fight against Duchenne Muscular Dystrophy

Dylan's fight against Duchenne Muscular Dystrophy

Still €643,525 to go. Help us build momentum.