33^rd Annual Miracle Tournament and Celebration Dinner

Treated at Children's Health in Dallas, TX.

When Jenifer was 20 weeks pregnant, she learned that her baby's, heart was on the right, instead of the left side of his body. This meant he would need surgery shortly after birth to help his blood flow properly. Kaleb's parents chose Children’s Health because not only would they have an expert surgeon, but an entire care team dedicated to their baby’s health. Kaleb was born six weeks early with a heart defect that impacted the way blood flowed through his lungs, meaning his pulmonary veins, which carry blood from the lungs to the heart, weren't working well. Kaleb’s doctors made the difficult decision to try a surgery that had only been performed once, unsuccessfully. Kaleb underwent surgery at 9 days old – placing two stints to keep oxygenated blood flowing throughout his body – and it worked so well that the procedure has become the standard of care for all babies born with this heart defect. He also lives with heterotaxy syndrome, a rare genetic disorder that can affect the development of important systems like the heart and gastrointestinal tract. Living with heterotaxy is difficult, unpredictable and requires long-term monitoring and care. But Kaleb’s care team and family do everything they can to keep him as healthy as possible, so he can focus on regular kid things — like swimming, Legos, Minecraft and learning everything he can about U.S. presidents. Every Halloween, Kaleb dresses up as a different U.S. president. He also loves animals, especially his Goldendoodle. “Her name is Jefferson, after President Thomas Jefferson. And yep, she’s a girl,” Kaleb said.

Thanks to donations to Children’s Miracle Network Hospitals, Kaleb had access to an innovative, life-saving heart surgeon and care team.

Treated at Kentucky Children’s Hospital in Lexington, KY.

At ?rst, eight-year-old Lucy’s parents thought she’d caught strep throat, or maybe the ?u. But as her symptoms progressed to a high fever and an upset stomach over the course of the week, they realized their daughter was dealing with something worse. Lucy’s pediatrician tested her for something called Multisystem In?ammatory Syndrome in Children, or MIS-C: a rare syndrome associated with COVID. “We were just ruling it out” was the mindset behind running blood work that led to Lucy’s diagnosis. “[Our pediatrician] said, ‘We’ve already called ahead to Kentucky Children’s Hospital, and they have a room for you. You need to go immediately.’” MIS-C can lead to major in?ammation of the organ systems, skin, and brain, and most children with the condition arrive at the hospital in bad shape. When Lucy was admitted, her blood pressure was low and her heart was beating way too fast. Lucy’s doctors and her parents quickly made the decision to transfer her to Kentucky Children’s Hospital’s pediatric intensive care unit (PICU). After several days in the PICU, Lucy’s condition began to improve. Soon she was discharged to recover fully at home. Lucy’s family is deeply grateful to the medical professionals at Kentucky Children’s Hospital for ensuring their story has a happy, healthy ending.

Thanks to donations to Children’s Miracle Network Hospitals, Lucy had access to lifesaving care at Kentucky Children’s as she recovered from MIS-C.

Treated at OHSU Doernbecher Children's Hospital in Portland, OR.

Ages 12 & 10

Madison (Maddie) has only known life with cystic fibrosis. A few days after she was born, she was transferred to OHSU Doernbecher Children’s Hospital for a bowel obstruction. After undergoing the procedure, she stayed in the neonatal intensive care unit (NICU) for 30 days. Two years later, Maddie’s little brother, Max, was also diagnosed with a bowel obstruction. His parents knew to go to the NICU at Doernbecher where his sister received care. Max’s severe bowel obstruction and jejunoileal atresia led to his diagnosis of cystic fibrosis too. As Maddie grew up, her condition began affecting her liver, and when she was 10, she was diagnosed with CF-associated liver disease. While their parents wouldn’t wish the diagnosis on either of their children, they see how Maddie and Max support each other on their shared health journeys. Maddie, now 12, loves art, playing golf and wants to be a veterinarian. 10-year-old Max is an all-star baseball player and his favorite position is shortstop. Maddie and Max continue to lean on one another as they manage their condition and are each other’s biggest cheerleaders.

Thanks to the support of Children’s Miracle Network Hospitals, Maddie and Max received quality care during their stay in the NICU at OHSU Doernbecher Children’s Hospital.