Junior Reporter

The Junior Reporter program, born from the partnership between University of Notre Dame Athletics and Beacon Health Foundation, gives Beacon Children’s Hospital patients the opportunity to meet and interview Notre Dame athletes. Meet these special kids, learn their stories and see them in action.

2024 Junior Reporter lineup

Get to know these amazing kids and find their full story and video below.

Nash Hensley

Sept. 7, 3:30 p.m.
Notre Dame vs. Northern IL
At nine days old, Nash was diagnosed with a genetic disorder called PKU, phenylketonuria, which means his body is missing an enzyme that helps break down protein. At four months old, Nash was also diagnosed with a form of dwarfism called achondroplasia. He’s likely the only child in America with these two disorders together. Nash has had surgeries and countless doctor and therapy visits at Beacon Children’s Hospital and will continue to for some time. Due to many complications at birth he was required to be on supplemental oxygen until past his second birthday. He walked with a walker and leg braces before gaining enough muscle strength to do it on his own. Nash’s mom, Angela, says, “He’s made me a stronger person. I think he’s made all of us stronger people.”

Braxton Miller

Sept. 21, 3:30 p.m.
Notre Dame vs. Miami University

Fifth-grader Braxton’s healthcare journey started when he complained to his parents about some stomach pain. After numerous medical visits, a suspected virus turned out to be something much more serious: acute lymphoblastic leukemia, a fast-growing cancer of the blood. Fortunately, Braxton’s illness responded to treatment immediately. In fact, the cancer cells died so quickly that the care team had to race to flush the released toxins out of his body. One month after treatment began, his cancer was in remission, and a few months after that, Braxton was the starting pitcher in a baseball game. Now that Braxton is one and one-half years into his treatment, there is no sign that the leukemia will return. With a smile, his mother, Päivi, says, “He’s going to have a happy, healthy life.” 

Avery Vinnedge

Sept. 28, 3:30 p.m.
Notre Dame vs. Louisville

On the first day of school in 2021, 6-year-old Avery woke up in the middle of the night with a fever. Off and on over the next six weeks, she would experience low-grade fevers and terrible leg pain. Multiple doctor’s visits and tests didn’t provide any definite answers. “The six weeks just felt like it was a lifetime,” said her mom, Kait. When worsening symptoms led to an emergency room visit, additional testing revealed that Avery had acute lymphoblastic leukemia. Aggressive treatment started right away, and she completed two years of treatment last December. “She’s so smart and so brave. We called her Ave the Brave during her treatment,” said Kait.

Greyson Young

Oct. 12, 3:30 p.m.
Notre Dame vs. Stanford

Greyson Young was born without any problems. But by his 9-month check-up, his head circumference had become extremely large. He was diagnosed with severe hydrocephalus, a buildup of cerebrospinal fluid in the ventricles deep within the brain. The extra fluid puts pressure on the brain and skull, which can cause brain damage and seizures. Greyson had brain surgery that same week. But not just any brain surgery: Dr. Daniel Fulkerson is one of the few pediatric neurosurgeons who specializes in a particular endoscopic option called ETV (endoscopic third ventriculostomy). Greyson’s surgery was a success, and Dr. Fulkerson says, “Greyson is doing fabulous. He’s shown no symptoms and encountered no problems so far. If he goes a full year without requiring another surgery, he’s probably cured for life.”

Gavyn Kimbrough

Nov 9th at 7:30 pm.
Notre Dave vs. FSU

It started out as a rash on his arms after football practice. Gavyn’s parents though he might just be having a simple allergic reaction to the grass. But before long, his rash had spread to his whole body. He tested negative for allergies. Next,  Gavyn’s joints began to swell, especially his fingers. He couldn’t walk. The hospital suspected juvenile arthritis. But a few days later, the results of additional testing showed the true culprit: Lyme disease. Fortunately, treatment with antibiotics for four weeks cleared his symptoms. Gavyn is now a healthy, adventurous, friendly and kind 10-year-old. Looking back, his mom Shayla says, “It was the scariest thing I’ve ever gone through.” But through it all, and with the help of his faith, her son kept his chin up. “He’s just a kid that doesn’t let things bother him too much. He’s a tough cookie for sure,” she said.