Thank you for supporting the Miracle Tournament. The silent auction is now operated by Bidding for Good at biddingforgood.com

Go to Auction

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

Mason
Age 8
Mason
Age 8

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.

ZaLayaa
Age 12
ZaLayaa
Age 12

Treated at Gillette Children's Specialty Healthcare in St. Paul, MN.

Twelve-year-old ZaLayaa has experienced a variety of sensory and complex medical conditions since she was an infant. Her symptoms have impacted her daily life, and to this day, their underlying cause remains a mystery. Over the years, her family has actively sought answers from doctors, heard different theories, and tried numerous treatments. Once they made it to Gillette Children’s Specialty Healthcare, her mom says “that made a world of difference.” Gillette’s medical team brought a new approach to ZaLayaa’s care. Rather than focusing on solving the puzzle of her diagnosis, her care team addresses the real-life issues ZaLayaa was facing every day. Now, she sees more than 25 different providers at Gillette, receiving comprehensive evaluations with pediatric medicine and rehabilitation specialists, along with numerous physical and occupational therapy appointments. Gillette’s therapeutic recreation specialists have allowed her to enjoy an accessible playground and an adaptive bicycle. She has been waterskiing, run from third base to home plate at a Minnesota Twins game, and impressed fellow golfers with her swing on the course.

The support of Children’s Miracle Network Hospitals has allowed ZaLayaa to reach new milestones on her health journey with innovative complex care teams and Therapeutic Recreation.

Jaxon
Age 8
Jaxon
Age 8

Treated at Nicklaus Children's Hospital in Miami, FL.

After a seemingly healthy pregnancy, Jaxon’s parents were told not to worry by medical providers by a few early signals that something seemed off. Thankfully, his uncle noticed the ridge along Jaxon’s forehead and did not believe the triangular shape of Jaxon’s head was caused by the trauma of delivery. At two weeks old, a CAT scan confirmed Jaxon’s metopic craniosynostosis, where the soft spot at the top of his head had been prematurely fused together in the womb. Jaxon’s parents took him to the renowned Nicklaus Children’s Hospital Brain Institute. At seven months old, Jaxon underwent an eight-hour cranial procedure at Nicklaus Children’s. Despite the challenges, he was in good hands, even combatting other anomalies such as the misalignment of the eyes, a hole in his heart, a horseshoe-shaped kidney, and more. Given the range of birth defects their son faced, Jaxon’s parents’ genetics testing at Nicklaus Children’s confirmed that he had a rare gene mutation in CDK13. There wasn’t much known about CDK13 at the time. Today, nearly 300 cases have been identified globally. For now, Jaxon’s parents treat each symptom as it arises. He struggles with tasks requiring the use of his hands and motor skills, and his ADHD and moderate autism made everyday life and academic tasks challenging. And yet, he continues to make remarkable progress in physical therapy, occupational therapy, and speech therapy. Jaxon’s resilience and carefree, fun personality positively inspires all the lives he touches.

Donations to Children’s Miracle Network Hospitals support the clinical institutes and personalized care that allow Jaxon to make remarkable progress on his journey.

See All 2024 Champion Children >