33^rd Annual Miracle Tournament and Celebration Dinner

Treated at Cohen Children's Medical Center in New Hyde Park, New York.

At the age of three, Mason started having prolonged fevers. During these extended periods, he would be lethargic, irritable, and barely able to eat. Even with the bruises on his skin, Mason’s primary physician told his parents that it was just a virus. A month later, his mom knew something wasn’t right so she took Mason to the emergency department of Cohen Children’s Medical Center. Shortly after he was admitted, Mason was diagnosed with acute lymphoblastic leukemia. For three years, he underwent chemotherapy treatments and has also had long hospital stays due to infections or low white blood cell count. Today, Mason is in remission and celebrated it by ringing the bell. Mason loves life, baseball, and ice hockey.

Donations to Children’s Miracle Network Hospitals fund life-saving treatments that help kids like Mason and their families cope during hospital stays.

Treated at Children's Hospital of Philadelphia in Philadelphia, PA.

Porter was born with Down syndrome at Children’s Hospital of Philadelphia (CHOP), where the care team helped his family understand the medical, cognitive, and social complexities to ensure he could have the best quality of life. From the beginning, specialists provided education through their Trisomy 21 Symposiums, which helped Porter’s family build a support network of other families going through similar experiences. During the medical procedures and hospitalizations for respiratory illnesses, Porter’s family was grateful for the opportunity to participate in a few clinical trials through CHOP, helping to build a body of research that will pave a positive future for other individuals with intellectual disabilities. “Porter is thriving today because we’ve got a team that sees him as a person with a bright future,” his mom says, adding that “the team at CHOP has always been by our side.” Now 12 years old, Porter plays drums in the school band. He loves horseback riding, baseball, Tae Kwon Do, and Special Olympics swimming.

Thanks to the support of Children’s Miracle Network Hospitals, Porter and his family received incredible care and support, including music and art therapy.

Treated at Valley Children's Hospital in Madera, CA.

Davey Jean was born with a rare genetic disorder called 22q11.2 deletion syndrome (22q) and was faced with many 22q-related anomalies including congenital heart defects, cleft palate, developmental and speech delays, etc. At 30 weeks in utero, she was diagnosed with Tetralogy of Fallot, a compilation of four heart defects, and required open-heart surgery soon after her birth. By the time she was three years old, she was still non-verbal and used American Sign Language to communicate. Her parents learned that she had conductive hearing loss and would need ear surgery to help drain the fluid causing it. Davey Jean also went through two complex surgeries for her Atypical Submucosal Cleft Palate, which made it nearly impossible for her to form sounds and words. The ear, nose, and throat (ENT) department at Valley Children’s, along with the plastic surgery, audiology and speech therapy teams, all joined in an effort to help with Davey Jean’s hearing issues and speech delays. Today, she is able to communicate using words. Now ten years old, Davey Jean has already undergone five surgeries at Valley Children’s. She continues to see multiple specialists at Valley Children’s, as well as physical and occupational therapy. She is very active and enjoys playing with her friends and doing gymnastics. She loves going to the park and playing with her toys and her dog, Tater Tot.

Thanks to support from Children’s Miracle Network Hospitals, Davey Jean has been able to get the surgeries and critical care she needed.