Welcome to our family's journey

Welcome to our journey – a space where we share our story as a family raising two incredible sons with Duchenne Muscular Dystrophy (DMD).

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  • It’s not about how you get there…

    We had family visiting this weekend and spent a special day at the Little Rock Zoo. Mason used the power chair so he could save his strength and still be independent, and Dawson enjoyed a few rides on the chair too. With Duchenne, every bit of energy matters… saving strength now means Mason can enjoy…

  • This is why I fight.

    I constantly feel like I have to do more — for the Duchenne community, and most of all, for my boys. If I’m not raising awareness, I feel like I’m not doing everything I possibly can to help find a cure. Duchenne is always on our minds.We’re always thinking about how to fight it —…

  • Living in the Unknown

    Listening to “Roar” by Tim Timmons, and it’s hitting every corner of my heart today. We’re standing on the edge of another season of unknowns — the kind that press in on you, whisper fear, and try to steal your peace. Unknowns like:How long will we be gone? Will Dawson be accepted into the gene…