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'The clinical trials that are available are groundbreaking' : Minnesota family finds hope in MDA's support for son

Duchenne Muscular Dystrophy is a progressive genetic disorder that causes muscles to weaken over time.

AUGUSTA, Mo. — In the quaint town of Augusta, Missouri, where time seems to slow down, the Zull family is embarking on a race against the clock. Their story is one of unexpected challenges, unwavering community support, and newfound hope in the face of a life-altering diagnosis.

Augusta is a close-knit community of about 100 people, where neighbors are more like family. As Danny Zull describes, "It really is about a hundred people that just, they like to take care of each other." This sense of community became a crucial lifeline for the Zulls when their son, Rory, was born three years ago.

Rory quickly became the light of his parents' lives. Danny proudly shares, "Rory is a character. I mean, he is smart, he's funny, he's intuitive." But behind Rory's infectious personality lay a diagnosis that would rewrite their family's story.

The day that was supposed to be filled with the joy of learning their baby's gender took an unexpected turn. Amanda Zull recalls, "We were just waiting to hear boy or girl. And then we heard that it was a boy. But then you could tell that her tone changed and she got a little bit more serious."

The Zulls were confronted with unfamiliar, scary words: Duchenne Muscular Dystrophy, a progressive genetic disorder that causes muscles to weaken over time. The diagnosis cast a long shadow of fear over the family.

Credit: Mike Bush

Danny admits to his initial struggle, saying, "It was just, we were gonna live in misery. Just that all the things you see that was gonna happen right away. And I didn't have hope. Um, so I was in a dark place."

However, in their darkest hour, the Zulls discovered they weren't alone. The Muscular Dystrophy Association (MDA) stepped in, offering a beacon of support and optimism.

"They were like, other families are like yours. And, um, that is how we were able to join groups and reach out to other families going through what we were going through," Amanda said. 

Now, with MDA's help, Rory is part of a clinical trial that could rewrite the future for children with Duchenne. The Zulls' outlook has dramatically shifted. Amanda now sees a bright future: "When I think about the future now I see Rory, um, doing all the things we had dreamed for him to do."

Danny's perspective has also transformed. He says, "I can see the cure in my lifetime. You know, I, I can really see. And, and I hope that it's, it's around the corner."

In Augusta, where time seems to stand still, the Zulls race forward with newfound optimism. Their journey reminds us that in a world that often rushes by, true progress is measured not in leaps and bounds, but in hope and the celebration of every small step.

The impact of the MDA on the Zull family cannot be overstated. As Danny puts it, "The MDA has meant everything to us." Their story is a testament to the power of community, research, and never giving up hope.

Credit: Mike Bush

The all-local MDA Telethon produced and hosted by Mike Bush will air live from Grant's Farm on Sunday, Sept. 1 from 8 to 10 p.m. To donate: 314-425-5355 and text the word Donate.

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