33^rd Annual Miracle Tournament and Celebration Dinner

Treated at Medical University South Carolina Shawn Jenkins Children's Hospital in Charleston, SC.

At 48 hours old, Vinny was diagnosed with Hirschsprung's disease, a gastrointestinal disorder that affects the body’s ability to eliminate stool. Under the care of the team at MUSC Shawn Jenkins Children’s Hospital, Vinny underwent a 4.5-hour lifesaving surgery.

Vinny spent one month in the hospital recovering. Despite the hurdles associated with his condition, he defied the odds and blossomed into a healthy, vibrant kid. The compassionate care he received from MUSC staff played a pivotal role in Vinny's remarkable recovery and ongoing well-being. Vinny received follow-up care from special teams at MUSC Shawn Jenkins Children’s Hospital and has not required a return visit since he was ten.

Now 12 years old and in the sixth grade, Vinny is a lover of sports, and can often be found on the tennis court, hanging out with his two sisters, or surfing. His true passion is playing soccer. Last year, he was selected and traveled to Madrid, Spain, to compete in the Real Madrid World Challenge tournament!

Thanks to donations to Children’s Miracle Network Hospitals, Vinny had access to specialized care and world-class surgeons at MUSC Shawn Jenkins Children’s Hospital.

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.

Treated at Duke Children's in Durham, NC.

At 18 weeks pregnant with twins, Stephanie learned something was wrong. Braeden, “Baby B,” was diagnosed with hypoplastic left heart syndrome, one of the most severe congenital heart defects. The prognosis was unclear. After researching options, Braeden’s parents chose to go with Duke Children’s, where he could receive the outpatient care he needed close to home. In advance of his birth, the staff gave them a tour of the facilities and set up meetings with their surgeon to ask questions. Over the next couple of years, Braeden returned to Duke Children’s for heart catheters and two more big surgeries, and his parents found comfort in nurses and doctors who truly cared. The medical teams continue to find innovative ways to treat hypoplastic left heart syndrome so more kids like Braeden can live their lives to the fullest. Now Braeden is nine years old and his sense of humor makes everyone around him smile.

Thanks to the support of Children’s Miracle Network Hospitals, Braeden received world- class medical care close to home at Duke Children’s.