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 Carilion Children's in Roanoke, VA.

Ten-year-old Meg has a rare genetic condition called CTBP, and scoliosis. At the age of nine, Meg had a full spinal fusion once her curve hit 101 degrees, a surgery that saved her life. Thanks to her care team at Carilion Children’s, Meg has access to all the therapies, doctors, and equipment she needs close to home. Meg loves babies, puppies, her American Girl Dolls, and playing with her big sisters!

Thanks to donations to Children’s Miracle Network Hospitals, Meg has access to world-class doctors and surgeons treating her genetic condition and scoliosis at Carilion Children’s Hospital.

Treated at OHSU Doernbecher Children's Hospital in Portland, OR.

Ages 12 & 10

Madison (Maddie) has only known life with cystic fibrosis. A few days after she was born, she was transferred to OHSU Doernbecher Children’s Hospital for a bowel obstruction. After undergoing the procedure, she stayed in the neonatal intensive care unit (NICU) for 30 days. Two years later, Maddie’s little brother, Max, was also diagnosed with a bowel obstruction. His parents knew to go to the NICU at Doernbecher where his sister received care. Max’s severe bowel obstruction and jejunoileal atresia led to his diagnosis of cystic fibrosis too. As Maddie grew up, her condition began affecting her liver, and when she was 10, she was diagnosed with CF-associated liver disease. While their parents wouldn’t wish the diagnosis on either of their children, they see how Maddie and Max support each other on their shared health journeys. Maddie, now 12, loves art, playing golf and wants to be a veterinarian. 10-year-old Max is an all-star baseball player and his favorite position is shortstop. Maddie and Max continue to lean on one another as they manage their condition and are each other’s biggest cheerleaders.

Thanks to the support of Children’s Miracle Network Hospitals, Maddie and Max received quality care during their stay in the NICU at OHSU Doernbecher Children’s Hospital.