33^rd Annual Miracle Tournament and Celebration Dinner

Treated at Children's Hospital of The King's Daughters in Norfolk, VA.

At 11 years old, Sam’s parents noticed that something wasn’t quite right. The energetic, competitive tennis player said he felt tired all the time and was often cold, his appetite disappeared and he lost some weight. His pediatrician ordered bloodwork and a few hours later, called the family and asked them to bring Sam immediately to the emergency department at Children's Hospital of The King's Daughters (CHKD). Sam was diagnosed with T-cell leukemia and had a mass in his lungs, close to his heart. Sam was admitted to CHKD and immediately started treatment. A week later, his mass was barely visible. Although he was discharged, Sam returned to CHKD several more times over the next year for additional treatment. During his nine hospital stays, Sam realized how fortunate he was to have his mom and dad with him every step of the way. He decided that when his cancer treatment was over, he wanted to help other families by fundraising for CHKD. Two years after his initial trip to the emergency department, Sam was in remission and had raised more than $100,000 to help families with a child in the hospital. Today, Sam is back in school and focused on getting stronger. His family says they are incredibly thankful for Sam’s recovery, the staff at CHKD, and everyone who has donated to help CHKD patients and families.

Thanks to donations to Children’s Miracle Network Hospitals, Sam received quick, lifesaving treatment for his T-cell leukemia and is a strong, healthy 15-year-old.

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 Texas Children's Hospital in Houston, TX.

Kylea was born prematurely at 34 weeks in Kansas, and she tested positive for cystic fibrosis (CF). Her medical team thought it was a false positive since she had no symptoms. Months later, Kylea was still under five pounds. Her mom took her to the emergency center at a nearby children’s hospital in Missouri, where Kylea was admitted for jaundice. After a liver biopsy and other tests, including blood tests to look for the genetic mutations that cause CF, the family got confirmation: Kylea had two copies of delta F508, the most common genetic mutation that causes cystic fibrosis. Once she had an official diagnosis, Kylea’s family turned to Texas Children’s Hospital since they were ranked number one in pulmonology and offered a holistic approach to care. Her family moved to Houston, just in time for the new school year. Her childhood was filled to the brim with sports, dance, gymnastics, Girl Scouts, swimming, science camp, and trips to the zoo.

Today, she is 15 and studying French. She hopes to travel the world and study forensic psychology in college.

Thanks to donations to Children’s Miracle Network Hospitals, Kylea had access to world-class, holistic pulmonology care for cystic fibrosis.