33^rd Annual Miracle Tournament and Celebration Dinner

Treated at Children's National Hospital in Washington, D.C..

Mason was 12 weeks old when he had open heart surgery at Children’s National Hospital to repair his rare congenital heart condition: Tetralogy of Fallot. Before the surgery, his doctor made a crucial discovery—Mason had only one coronary artery and it was not in the right place—an additional congenital abnormality. While Mason’s care team didn’t know exactly what was to come, his Child Life specialist and Housing & Amenities Coordinator did an amazing job supporting his family during this uncertain time. Little details meant so much to his family, like bringing clothing to Mason’s mom during her stay, explaining things to his seven-year-old sister, and helping his grandparents travel to the hospital from Alabama. Mason is now 13 years old and has had a few surgeries since his initial procedure, and still remains connected to the hospital that saved his life. He loves playing video games, playing the saxophone and piano, making music, DJing and spending time with his family.

Thanks to donations to Children’s Miracle Network Hospitals, Mason had access to critical cardiac care to repair his heart condition, helping him lead a happy and healthy life.

Treated at Nicklaus Children's Hospital in Miami, FL.

After a seemingly healthy pregnancy, Jaxon’s parents were told not to worry by medical providers by a few early signals that something seemed off. Thankfully, his uncle noticed the ridge along Jaxon’s forehead and did not believe the triangular shape of Jaxon’s head was caused by the trauma of delivery. At two weeks old, a CAT scan confirmed Jaxon’s metopic craniosynostosis, where the soft spot at the top of his head had been prematurely fused together in the womb. Jaxon’s parents took him to the renowned Nicklaus Children’s Hospital Brain Institute. At seven months old, Jaxon underwent an eight-hour cranial procedure at Nicklaus Children’s. Despite the challenges, he was in good hands, even combatting other anomalies such as the misalignment of the eyes, a hole in his heart, a horseshoe-shaped kidney, and more. Given the range of birth defects their son faced, Jaxon’s parents’ genetics testing at Nicklaus Children’s confirmed that he had a rare gene mutation in CDK13. There wasn’t much known about CDK13 at the time. Today, nearly 300 cases have been identified globally. For now, Jaxon’s parents treat each symptom as it arises. He struggles with tasks requiring the use of his hands and motor skills, and his ADHD and moderate autism made everyday life and academic tasks challenging. And yet, he continues to make remarkable progress in physical therapy, occupational therapy, and speech therapy. Jaxon’s resilience and carefree, fun personality positively inspires all the lives he touches.

Donations to Children’s Miracle Network Hospitals support the clinical institutes and personalized care that allow Jaxon to make remarkable progress on his journey.

Treated at Children's Hospital Los Angeles in Los Angeles, CA.

Melody was born with a rare congenital condition where string-like bands of tissue wrap around fingers and toes. Amniotic band syndrome is non-preventable and affects one in 15,000 births annually. Melody faced her condition with grace and her family was referred to Children’s Hospital Los Angeles, where she has received comprehensive support. To date, Melody has had four surgical procedures to separate her fingers and remove excess skin to improve her hands’ functionality. Today, Melody proudly tells people about her unique hands. She loves doing art and celebrates her uniqueness.

Thanks to support from Children’s Miracle Network Hospitals, Melody has received access to donor-funded programs, providing a lifeline of support for the areas of greatest need in children’s health care.