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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

Natalie
Age 15
Natalie
Age 15

Treated at UNM Children’s Hospital in Albuquerque, NM.

Natalie’s cancer journey began at the age of ten when her mom noticed her daughter’s visual impairment. She was diagnosed with an Optic Pathway Glioma, a type of cancer that is difficult to treat and can also affect the pituitary gland. After two chemotherapy sessions, the tumor had completely disappeared, and her family rejoiced. She continued chemotherapy for another year as neurologists monitored Natalie.

A few months later, an MRI identified an area of concern and a biopsy confirmed Anaplastic Astrocytoma, a different, more aggressive brain tumor. She immediately and courageously began treatment again, including 30 rounds of proton therapy radiation and 42 rounds of oral chemotherapy.

Although her treatment worked, she was left with hemiparesis, the weakness of her right side weakness, which required two years in physical and occupational therapy. Recently, an MRI detected a new area of concern, this time, in Natalie’s brain stem. To get a biopsy, Natalie needed major surgery to access the tumor through her cerebellum. Doctors found a Germinoma tumor and her family was relieved to learn that the condition is very treatable. Now, Natalie is bravely facing months of chemotherapy again at UNM Children’s Hospital.

Donations to Children’s Miracle Network Hospitals benefited Natalie’s highly tailored care throughout her journey.

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.

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.

See All 2024 Champion Children >