33^rd Annual Miracle Tournament and Celebration Dinner

Treated at Children's Hospital Colorado in Aurora, CO.

At age 4, Maelle began to complain that her head hurt and her eyes started crossing. Doctors discovered a three-centimeter mass in her brain and immediately sent the family to Children’s Hospital Colorado where Maelle had a biopsy.

Doctors at Children’s Hospital Colorado diagnosed Maelle with a non-cancerous pilocytic astrocytoma. Due to the tumors’ precarious location, it was deemed inoperable. After careful consideration, Maelle’s family and care team decided to shrink the tumor with chemotherapy. After seven months of chemotherapy, the tumor had shrunk significantly, and they were able to cease treatment and return to normal life.

For two years, Maelle enjoyed life outside of the hospital and became an avid volleyball player. But unfortunately, during a routine check-up, doctors discovered that Maelle’s tumor had started growing again. In January of 2021, Maelle began a new experimental treatment to help reduce the growth of the tumor. Maelle continued to remain in the best of spirits and came off the treatment in February of 2023.

Whilst the treatment saw limited success, she has been off all medication since. Maelle continues to visit Children’s Hospital Colorado to monitor the tumors’ progress and is excited to start high school next year! The family has hope in the groundbreaking research being conducted at Children’s Hospital Colorado to find new treatments and therapies for kids like Maelle.

“Words can’t describe what Children’s Colorado means to us,” says her mom, Kristen. “A hospital isn’t a place where most people would choose to be. And yet, I always feel at ease here, knowing that our daughter is getting the best care available. They are nothing short of amazing.”

Thanks to donations to Children’s Miracle Network Hospitals, Maelle benefits from groundbreaking research being conducted by her local member hospital.

Treated at University of Michigan Health at Sparrow Children's Center in Lansing, MI.

At 17 weeks pregnant, Ryan’s mom, Becky, was diagnosed with a subchorionic hematoma. Soon after, Becky was placed on bedrest for 6 weeks until Ryan was born via an emergency C-section at 23 weeks.

Ryan weighed one pound seven ounces at birth. In the University of Michigan Health at Sparrow Children’s Center’s Regional Neonatal Intensive Care Unit (RNICU), he was supported by a team of neonatologists, nurse practitioners, nurses, respiratory therapists, phlebotomists, and many others. Ryan’s time in the NICU was marked by underdeveloped lungs and bronchopulmonary dysplasia, multiple infections, intraventricular hemorrhages, necrotizing enterocolitis, and advanced retinopathy of prematurity.

After discharge, Ryan required regular follow-up appointments with many subspecialists, therapists, medical equipment providers, and others. He was readmitted that first year into the pediatric intensive care unit for breathing difficulties, and additional surgery.

Today, Ryan is a 14-year-old who exemplifies perseverance. He loves to build things, ride his bike and hoverboard, and play in the band!

Thanks to donations to Children’s Miracle Network Hospitals, Ryan had access to a team of lifesaving specialists in the neonatal intensive care unit after being 17 weeks prematurely.

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.