33^rd Annual Miracle Tournament and Celebration Dinner

Treated at St. Rose Dominican Hospital in Las Vegas, NV.

Sixteen years ago, Colbie and Kenna’s parents were excitedly expecting their first children, twin girls. Everything was routine until their mother noticed some discomfort and headed to the hospital. Staff at St. Rose Dominican Hospital quickly determined that something wasn’t right. At 23 weeks and 3 days pregnant, she was slowly leaking amniotic fluid. After doing everything medically possible to delay the birth, the girls were born 15 weeks early. Colbie weighed just 1lb 6oz and Kenna weighed 1lb 5oz. The girls were in the neonatal intensive care unit for 113 days. They each faced their own struggles and were still on oxygen, but one week after their original due date, they were finally able to go home. They continued to grow and develop without any major delays. Today the girls are doing better than ever. Kenna plays competitive soccer and is on the varsity track team. Colbie is part of the National Honors Society and plays the electric guitar. Both girls volunteer for the Unified Special Olympics through their school district.

Thanks to donations to Children’s Miracle Network Hospitals, Colbie and Kenna had access to lifesaving care in the neonatal intensive care unit after being born 15 weeks prematurely.

Treated at Nationwide Children’s Hospital in Toledo, OH.

Two weeks before Myla’s sixth birthday she was diagnosed with acute lymphoblastic leukemia. Myla’s diagnoses came during the COVID-19 pandemic, therefore, Myla’s dad had to wait out in the van while they remained in the emergency room. It was through a video call that he heard the words “your child has cancer.” Myla initially spent ten days in the hospital where she had surgery to have her port placed, receive her first few rounds of chemotherapy, and many blood transfusions. After her release from the hospital, Myla began experiencing severe neuropathy. She had difficulty walking, using her hands, and her vocal cords were becoming paralyzed. Myla tested positive for Charcot-Marie-Tooth disease (CMT). Two weeks later, she was sent home with many mobility and occupational therapy devices to help her regain her independence.

Today, Myla is nine and has returned to things she loved to do before her diagnosis- like riding a bike, doing ballet, and going to school. Myla keeps a smile on her face and takes things one day at a time!

Thanks to donations to Children’s Miracle Network Hospitals, Myla had access to the therapies, specialists, and equipment that helped her overcome leukemia and get back to all her favorite activities.

Treated at Duke Children's in Durham, NC.

At 18 weeks pregnant with twins, Stephanie learned something was wrong. Braeden, “Baby B,” was diagnosed with hypoplastic left heart syndrome, one of the most severe congenital heart defects. The prognosis was unclear. After researching options, Braeden’s parents chose to go with Duke Children’s, where he could receive the outpatient care he needed close to home. In advance of his birth, the staff gave them a tour of the facilities and set up meetings with their surgeon to ask questions. Over the next couple of years, Braeden returned to Duke Children’s for heart catheters and two more big surgeries, and his parents found comfort in nurses and doctors who truly cared. The medical teams continue to find innovative ways to treat hypoplastic left heart syndrome so more kids like Braeden can live their lives to the fullest. Now Braeden is nine years old and his sense of humor makes everyone around him smile.

Thanks to the support of Children’s Miracle Network Hospitals, Braeden received world- class medical care close to home at Duke Children’s.