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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

Gabby
Age 15
Gabby
Age 15

Treated at Children's Specialized Hospital in Mountainside, New Jersey.

Thirteen-year-old Gabriella (Gabby) was running at track practice when suddenly she felt her left arm drop on her last lap. After she lost feeling in her arm, she quickly lost sensation in her left leg and fell to the ground. Gabby was rushed to the pediatric unit of a local trauma center. The hospital immediately took her for a CAT scan, which revealed a brain bleed. After several tests, the doctors diagnosed Gabby with a rare brain arteriovenous malformation (AVM) rupture in her right frontal lobe.

She had to wait 10 days for a craniotomy to remove the AVM because they needed the blood to settle in her brain. A few days after surgery, Gabby was transferred to Children’s Specialized Hospital (CSH) for inpatient therapy. AVMs cause stroke-like symptoms, in Gabby’s case, paralysis of the left side of her body and facial weakness. For 19 days in a pediatric intensive care unit, Gabby couldn’t move or sit up. During the five weeks she spent at CSH, Gabby received physical, occupational, speech, and recreational therapies, including aquatic therapy and targeted ways to help her walk again and smile symmetrically. Gabby arrived wheelchair-bound and successfully walked out of CSH on her own. Since then, started practicing soccer and lacrosse again.

Donations to Children’s Miracle Network Hospitals helped Gabby benefit from various forms of therapies that supported her road to recovery.

Addison
Age 11
Addison
Age 11

Treated at West Virginia University Children’s in Morgantown, WV.

Addison was eight years old when she had a rapid onset of seizures, which were misdiagnosed as panic attacks. Doctors encouraged her family to take their already scheduled vacation, but after arriving in South Carolina, her episodes increased in intensity and frequency. When her mom took her to the nearest emergency department, she was told it would be a thirteen-hour wait. Addison’s eyes were dilated and her hands and legs were shaking; her mother wondered if her daughter was having seizures and pleaded for a doctor to admit her daughter. After countless tests and doctors’ visits, neurologists diagnosed her with cortical dysplasia to the frontal lobe, which is a congenital abnormality of brain development that can cause irretractable epilepsy. Addison underwent a craniotomy with right frontal lobe resection and a few weeks later, she needed a spinal tap to drain the excess fluid from her brain due to a cerebrospinal fluid leak. Today, although on medication and still having seizures, Addison exudes strength and wisdom far beyond her years. When she grows up, Addison wants to become a Child Life specialist.

Donations to Children’s Miracle Network Hospitals provides life-saving care and essential programs that support Addison and her family during her treatments.

Porter
Age 12
Porter
Age 12

Treated at Children's Hospital of Philadelphia in Philadelphia, PA.

Porter was born with Down syndrome at Children’s Hospital of Philadelphia (CHOP), where the care team helped his family understand the medical, cognitive, and social complexities to ensure he could have the best quality of life. From the beginning, specialists provided education through their Trisomy 21 Symposiums, which helped Porter’s family build a support network of other families going through similar experiences. During the medical procedures and hospitalizations for respiratory illnesses, Porter’s family was grateful for the opportunity to participate in a few clinical trials through CHOP, helping to build a body of research that will pave a positive future for other individuals with intellectual disabilities. “Porter is thriving today because we’ve got a team that sees him as a person with a bright future,” his mom says, adding that “the team at CHOP has always been by our side.” Now 12 years old, Porter plays drums in the school band. He loves horseback riding, baseball, Tae Kwon Do, and Special Olympics swimming.

Thanks to the support of Children’s Miracle Network Hospitals, Porter and his family received incredible care and support, including music and art therapy.

See All 2024 Champion Children >