33^rd Annual Miracle Tournament and Celebration Dinner

Treated at CHRISTUS Children’s in San Antonio, TX.

Drew was a happy, healthy two-year-old who had never been ill. He never even had an earache before he was diagnosed with pneumonia and admitted into the H-E-B Emergency Department at CHRISTUS Children’s after a very high fever. When pneumonia didn’t improve, he was transferred to the pediatric intensive care unit (PICU) and underwent surgery to clear out his lungs, followed by a blood transfusion the next day. Drew’s vitals dropped extremely low, causing him to go into cardiac arrest. After his second surgery, he was able come off the ventilator, but then his anaphylactic allergic reaction to antibiotics caused another setback. His mother says “the PICU team will always have a special place in our hearts. They gave us the greatest gift: Drew’s life.” Today, Drew has fully recovered. He is a fun-loving, sweet nine-year-old that loves Marvel and LEGOS. He stays busy on the weekends playing football, baseball, and basketball.

Thanks to the support of Children’s Miracle Network Hospitals, Drew benefited from a brand new PICU ventilator to support his complex care and Child Life services for his family.

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 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.