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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

Celeste
Age 5
Celeste
Age 5

Treated at Orlando Health Arnold Palmer Hospital for Children in Orlando, FL.

During their 20-week ultrasound, Akosua and Fernando learned that their baby had spina bifida. Determined to explore all options, they reached out to the Fetal Care Center at Orlando Health Winnie Palmer Hospital for Women and Babies after learning the hospital offered in-utero surgery for babies with this diagnosis. Within a week, Akosua started an evaluation to see if she and her baby were suitable for in-utero surgery, and thankfully, they were. At 25 weeks into her pregnancy, Akosua underwent surgery to correct the defect in Celeste’s spine. Seven weeks later, Celeste was born, weighing 4 pounds, 10 ounces. After a short stay in the neonatal intensive care unit to ensure her health, she was able to go home. Now, at five years old, Celeste is thriving. She walks on her own and enjoys gymnastics, swimming and playing with her sister. Celeste is smart, playful, determined and kind. Celeste goes to weekly physical therapy, and as she grows, she will continue to receive care at the Spina Bifida Clinic at Orlando Health Arnold Palmer Hospital for Children.

Donations to Children’s Miracle Network Hospitals helped fund the fetal surgery program and the state-of-the-art ultrasound machine used to detect spina bifida in kids like Celeste.

Colbie & Kenna
Colbie & Kenna

Treated at St. Rose Dominican Hospital in Las Vegas, NV.

Sixteen years ago, Colbie and Kenna’s parents were excitedly expecting their first children, twin girls. Everything was routine until their mother noticed some discomfort and headed to the hospital. Staff at St. Rose Dominican Hospital quickly determined that something wasn’t right. At 23 weeks and 3 days pregnant, she was slowly leaking amniotic fluid. After doing everything medically possible to delay the birth, the girls were born 15 weeks early. Colbie weighed just 1lb 6oz and Kenna weighed 1lb 5oz. The girls were in the neonatal intensive care unit for 113 days. They each faced their own struggles and were still on oxygen, but one week after their original due date, they were finally able to go home. They continued to grow and develop without any major delays. Today the girls are doing better than ever. Kenna plays competitive soccer and is on the varsity track team. Colbie is part of the National Honors Society and plays the electric guitar. Both girls volunteer for the Unified Special Olympics through their school district.

Thanks to donations to Children’s Miracle Network Hospitals, Colbie and Kenna had access to lifesaving care in the neonatal intensive care unit after being born 15 weeks prematurely.

London
Age 9
London
Age 9

Treated at Hasbro Children's Hospital in Providence, RI/New Bedford, MA.

At 18 weeks gestation, London’s parents wanted to find out their baby’s gender. A high-level ultrasound soon confirmed that their baby was a girl--and that she would be born with spina bifida. Her parents did everything they could to learn about the diagnosis in preparation. Dr. Petra Klinge, a neurosurgeon at Hasbro Children’s Hospital, not only reassured them, but she also gave them hope. The day after London was born, Dr. Klinge performed an intricate eight-hour surgery to close the skin and spinal cord on the tiny newborn’s spine. When London was still not walking at 18 months, early intervention specialists advised her parents to consider leg braces and a walker, but instead they turned to Hasbro’s Pediatric Rehabilitation team and continued physical therapy. Just after turning two years old, London got up and walked across the room for the first time on her own. Now nine years old, London loves to dance and play soccer, and she is training for a Black Belt. She continues to amaze everyone with her vibrant smile and personality.

Donations to Children’s Miracle Network Hospitals helped London get the support of her local pediatric rehabilitation program.

See All 2024 Champion Children >