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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

Kaleb
Age 12
Kaleb
Age 12

Treated at Children's Health in Dallas, TX.

When Jenifer was 20 weeks pregnant, she learned that her baby's, heart was on the right, instead of the left side of his body. This meant he would need surgery shortly after birth to help his blood flow properly. Kaleb's parents chose Children’s Health because not only would they have an expert surgeon, but an entire care team dedicated to their baby’s health. Kaleb was born six weeks early with a heart defect that impacted the way blood flowed through his lungs, meaning his pulmonary veins, which carry blood from the lungs to the heart, weren't working well. Kaleb’s doctors made the difficult decision to try a surgery that had only been performed once, unsuccessfully. Kaleb underwent surgery at 9 days old – placing two stints to keep oxygenated blood flowing throughout his body – and it worked so well that the procedure has become the standard of care for all babies born with this heart defect. He also lives with heterotaxy syndrome, a rare genetic disorder that can affect the development of important systems like the heart and gastrointestinal tract. Living with heterotaxy is difficult, unpredictable and requires long-term monitoring and care. But Kaleb’s care team and family do everything they can to keep him as healthy as possible, so he can focus on regular kid things — like swimming, Legos, Minecraft and learning everything he can about U.S. presidents. Every Halloween, Kaleb dresses up as a different U.S. president. He also loves animals, especially his Goldendoodle. “Her name is Jefferson, after President Thomas Jefferson. And yep, she’s a girl,” Kaleb said.

Thanks to donations to Children’s Miracle Network Hospitals, Kaleb had access to an innovative, life-saving heart surgeon and care team.

Joseph
Age 12
Joseph
Age 12

Treated at Bernard & Millie Duker Children's Hospital at Albany Medical Center in Albany, NY.

During Joseph’s newborn screening, a blood test flagged a rate metabolic genetic disorder, called galactosemia. Galactosemia prevents the body from breaking down the sugar galactose, causing it to build up in the blood and wreak havoc on organs. While waiting for further test results, Joseph was admitted to the emergency room with a fever, and at that point had become septic, which eventually resulted in meningitis. Doctors prescribed him strong antibiotics, which was lifesaving, but unfortunately caused unilateral hearing loss.

Because of galactosemia, Joseph must adhere to a strict diet. There currently is no treatment or cure for galactosemia, only dietary restrictions. His family has become creative chefs, finding new recipes and workarounds to meet Joseph’s dietary needs.

Today, Joseph is 12 years old. He enjoys soccer, swimming, riding his bike, and playing fortnight. Last year, Joseph obtained his black belt in taekwondo.

Donations to Children’s Miracle Network Hospitals help patients and families like Joseph’s receive ongoing, specialized care.

Libbi
Age 5
Libbi
Age 5

Treated at Golisano Children's Hospital of Southwest Florida in Fort Myers, FL.

At just 20 months old, Libbiana (Libbi) was diagnosed with stage 2 Wilms tumor in the height of the pandemic. On the day that Libbi was planning to ring the bell to celebrate being cancer-free at Golisano Children’s Hospital, her family learned that the cancer had come back and that it was growing rapidly. It consumed Libbi’s entire abdominal and pelvic area, compressing her bladder, intestines, and lungs. Despite strong chemotherapy, the tumor wasn’t shrinking. A risky and complicated surgery became the only option for her survival. Thankfully, by the time Libbi turned three, she had beat Wilms tumor twice. Over the course of 150 nights and an additional 150 days in the oncology clinic, Libbi overcame major emergency surgeries, being on a ventilator, blood and platelet transfusions, the removal of a kidney, intensive chemotherapy, and so much more. Today, Libbi is five years old, cancer-free, and healthy. She and her family love to share her story to give hope to other families.

Donations to Children’s Miracle Network Hospitals ensured that Libbi and her family had the care and support they needed as she fought to beat cancer.

See All 2024 Champion Children >