33^rd Annual Miracle Tournament and Celebration Dinner

Treated at CHOC Hospital in Orange, CA.

Cash was 13 years old when he was playing football in a park and collapsed on the field. He went into cardiac arrest and the paramedics arrived within minutes. After repeated shocks and IV medication in the local emergency room, he was transported to CHOC Hospital to receive care from a recently formed collaboration between CHOC and UCLA Health pediatric heart specialists. The specialists diagnosed Cash with an anomalous left coronary artery (ALCA), a rare condition that disrupts the flow of blood to the heart. Since only one percent of the population is born with it, sudden cardiac arrest during exertion may be the first sign of ALCA and that’s what happened to Cash. He spent 33 days at CHOC Hospital before he was stable enough to go home. Now 15, Cash manages his condition with medications to support optimal heart function. Cash does his best to stay positive, spends time with family and friends, and enjoys traveling to new places.

Thanks to support for Children’s Miracle Network Hospitals, Cash was able to receive life-saving surgery and highly specialized care.

Treated at Johns Hopkins All Children’s Hospital in St. Petersburg, FL.

You would never know by looking at Gavin that he spent the first five years of his life battling debilitating ailments and undergoing countless treatments for an undiagnosed disease. Gavin was just three months old when he started experiencing persistent high fevers, rashes, vomiting, and blood in his intestinal tract. Early tests confirmed elevated liver enzymes and inflammatory markers in his blood. Gavin received treatment for his symptoms, but nothing seemed to cure the cause. When he was just two years old, Gavin had surgery for his kidneys at Johns Hopkins All Children’s Hospital. The surgery was successful, but Gavin continued to suffer from his ailments. For the next three years, Gavin endured several colonoscopies, biopsies, and MRIs without a definite diagnosis. At five years old, after discovering ulcers throughout Gavin’s intestinal tract, he was diagnosed with Crohn’s disease- an inflammatory bowel disease that causes chronic inflammation in the intestinal tract. Crohn’s disease is rare in young children and often undetectable. Today, he receives IV infusion treatments every four weeks and is living a much healthier life. Gavin is an 12-year-old who loves all things golf-related, riding roller coasters, swimming, reading, and has a zest for life.

Thanks to the support of Children’s Miracle Network Hospitals, Gavin received a diagnosis and receives ongoing infusion treatment help improve his quality of life.

Treated at Boston Children’s Hospital in Boston, MA.

The joy of Kennedy’s birth changed to fear when she stopped feeding and her oxygen levels dropped. After six weeks with no answers at a local hospital, Kennedy’s parents drove 90 minutes to Boston Children’s Hospital, where extensive testing revealed Kennedy had a rare condition where her weak trachea could collapse to block the airway, making it hard to breathe. Her doctor explained that Kennedy needed a tracheotomy to keep her airway stable. After 136 days at Boston Children’s, nine-month-old Kennedy was able to go home. The care team helped the family understand how to access benefits for children with complex medical needs, including the care of an at-home nurse. Six years later, Kennedy visits Boston Children’s for check-ups and is making great progress, working toward being able to walk on her own. Kennedy is a proud big sister and loves music and seeing her friends at school.

Donations to Children’s Miracle Network Hospitals supported Kennedy over her 136 days of care with Child Life Specialists, music therapy, and visits from therapy dogs.