33^rd Annual Miracle Tournament and Celebration Dinner

Treated at Levine Children's Hospital in Charlotte, NC.

At nine years old, Gracie found a bump below her ribs. After an ultrasound and an MRI, the doctors didn’t think the bump was cancerous, but they did a biopsy just in case. It took over two weeks to receive a final diagnosis: a rare soft tissue cancer called CIC-DUX4 sarcoma. Since there had been less than 200 reported cases to date, there was no definitive treatment plan. Over the next six months, Gracie underwent surgery, intensive chemotherapy, and IV infusions at Levine Children’s Hospital. Now in remission, 11-year-old Gracie helps other kids fighting cancer and lights up every room she enters. She returned to school as a fifth grader and is back to her favorite past time: playing soccer.

Thanks to the support of Children’s Miracle Network Hospitals, the Child Life program at Levine Children’s Hospital has the resources needed to give kids like Gracie the best and most comfortable care.

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.

Treated at Carilion Children's in Roanoke, VA.

Ten-year-old Meg has a rare genetic condition called CTBP, and scoliosis. At the age of nine, Meg had a full spinal fusion once her curve hit 101 degrees, a surgery that saved her life. Thanks to her care team at Carilion Children’s, Meg has access to all the therapies, doctors, and equipment she needs close to home. Meg loves babies, puppies, her American Girl Dolls, and playing with her big sisters!

Thanks to donations to Children’s Miracle Network Hospitals, Meg has access to world-class doctors and surgeons treating her genetic condition and scoliosis at Carilion Children’s Hospital.