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33rd Annual Miracle Tournament and Celebration Dinner

The 33rd Annual Miracle Tournament and Celebration Dinner benefiting Children's Miracle Network Hospitals, will take place June 24-25, 2024. We look forward to welcoming everyone to the NCR Country Club in Kettering, Ohio for the tournament and the National Museum of the United States Air Force in Dayton, Ohio for the Celebration Dinner*. Last year, more than 600 suppliers, vendors and business partners participated in the tournament or attended the Celebration Dinner*, interacting with Champion Children and their families. Thanks to their generous support, we were able to raise nearly $3 million for children’s hospitals across the United States.

*Celebration Dinner is by invitation only and reserved for Event Sponsors.

Join us June 24-25, 2024!

“We could not be more grateful for the incredible support of corporate partners like 7-Eleven, Inc., who, year in and year out, amaze us with their passion for our cause. Together with their customers, suppliers, vendors, Franchise Owners and employees, the impact of their fundraising efforts is helping us change kids’ health to change the future.”

- Aimee J. Daily, Ph.D.
President and CEO, Children’s Miracle Network Hospitals

Contact Info

Contact us at
GM-MiracleTournament@7-11.com

2024 Champion Children

Carah
Age 17
Carah
Age 17

Treated at Dayton Children’s Hospital in Dayton, OH.

At the age of three, Carah was diagnosed with childhood-onset fluency disorder (also known as stuttering). While most children outgrow a stutter by the age of 5, Carah did not. In 6th grade, a substitute teacher mocked her in class, leaving Carah spiraling with her self-esteem and confidence plummeting. She mentally and emotionally struggled and didn’t want to go to school. Carah saw countless speech therapists over the years but never felt there was a right fit as the focus was placed on her speech fluency and less on the deep, lingering emotional trauma she was experiencing. That changed when Carah turned to Dayton Children’s Speech Therapy Program. “...from the time we walked through those speech therapy doors, they took the time to actually talk with Carah and dug deeper to the parts that people can’t see. And helped Carah in learning tools and techniques to navigate those feelings and mental roadblocks,” her mom said. Carah will always have a stutter; however, she’s learned that her condition does not steal the power of her own voice. One way she’s doing that is by educating her former middle school by giving a keynote speech every year, now part of her school’s curriculum, about stuttering, understanding yourself and your feelings, and bullying. “Stuttering is a part of me, but it doesn’t define me. I have a lot of goals set for the future and I’m just getting started,” Carah said.

Thanks to donations to Children’s Miracle Network Hospitals, Carah received life-changing support from Dayton Children’s Speech Therapy Program, helping her self-esteem grow as she navigates Child Onset Fluency Disorder.

Benjamin
Age 6
Benjamin
Age 6

Treated at Penn State Health Children's Hospital in Lancaster, PA.

When Benjamin was born a month early, medical staff realized immediately that he wasn’t crying or breathing correctly. “Everything that could be wrong with his lungs seemed to be wrong,” said Ben's mom, Danielle. He was transported by a pediatric ambulance that was funded by Children's Miracle Network Hospitals to Penn State Health Children’s Hospital, which had the highest level NICU and a high-oscillating ventilator that could save his life. Because Benjamin’s condition was so critical, a doctor explained that he may need a form of life-support called ECMO, a machine that was also purchased by Children’s Miracle Network Hospitals. “I remember signing the consent for the ECMO and asking the doctor if we have to go to ECMO, and that doesn’t work, is there anything beyond that? And she said no. Knowing that we were at that point was very scary,” shared Danielle. “But he’s a strong guy. He rallied and did so well.” A few weeks later, Benjamin was able to go home, and today is a happy, healthy kid! Benjamin loves baseball, soccer and Cub Scouts. He loves trains, bridges, and building things with Legos. He also loves the Pittsburgh Steelers and got to go to Pittsburgh to attend his first game!

Thanks to donations to Children’s Miracle Network Hospitals, Benjamin received life-saving care with the use of a pediatric ambulance and ECMO machine, allowing him to live a healthy life.

Kylea
Age 15
Kylea
Age 15

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.

See All 2024 Champion Children >