33^rd Annual Miracle Tournament and Celebration Dinner

Treated at Penn State Health Children's Hospital in Lancaster, PA.

When Benjamin was born a month early, medical staff realized immediately that he wasn’t crying or breathing correctly. “Everything that could be wrong with his lungs seemed to be wrong,” said Ben's mom, Danielle. He was transported by a pediatric ambulance that was funded by Children's Miracle Network Hospitals to Penn State Health Children’s Hospital, which had the highest level NICU and a high-oscillating ventilator that could save his life. Because Benjamin’s condition was so critical, a doctor explained that he may need a form of life-support called ECMO, a machine that was also purchased by Children’s Miracle Network Hospitals. “I remember signing the consent for the ECMO and asking the doctor if we have to go to ECMO, and that doesn’t work, is there anything beyond that? And she said no. Knowing that we were at that point was very scary,” shared Danielle. “But he’s a strong guy. He rallied and did so well.” A few weeks later, Benjamin was able to go home, and today is a happy, healthy kid! Benjamin loves baseball, soccer and Cub Scouts. He loves trains, bridges, and building things with Legos. He also loves the Pittsburgh Steelers and got to go to Pittsburgh to attend his first game!

Thanks to donations to Children’s Miracle Network Hospitals, Benjamin received life-saving care with the use of a pediatric ambulance and ECMO machine, allowing him to live a healthy life.

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 Tucson Medical Center for Children in Tucson, AZ.

In 2017, Brielle was born with a condition called Amniotic Band Syndrome, which affected all of her extremities. The surgeons at Tucson Medical Center for Children helped correct some of her limb differences during her first year of life, which has helped her meet some key milestones. During the pandemic, she suffered from Multisystem inflammatory syndrome in children (MIS-C)-19 and was hospitalized for a week. During that time, she received treatment to help her overcome this rare and unfamiliar illness, which is known to be life-threatening. Today, she’s six years old, and excelling in school. She recently received the Stars of Honor Award.

Thanks to donations to Children’s Miracle Network Hospitals, patients like Brielle can access customized care that best suits their needs.