33^rd Annual Miracle Tournament and Celebration Dinner

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.

Treated at Cook Children's Medical Center in Fort Worth, TX.

Less than two weeks after Molly started experiencing numbness in her face, she was diagnosed with Ewing sarcoma, a type of cancer that forms in bone or soft tissue. Molly underwent brain surgery to remove the tumor and has recently finished chemotherapy. Molly’s dad said that while he could never have imagined hearing the word cancer, he finds comfort in knowing how much the hospital staff cares for his daughter. “Cook Children’s is a big part of this new life that we have to live while we get through this season,” he said. “It’s not just us fighting this fight. While the journey hasn’t been easy, Molly has worked to express any fears and concerns with the support of Child Life specialists.”

Donations to Children’s Miracle Network Hospitals helps families like Molly’s with support during her hospital stays and preparation for care at home.

Treated at Riley Hospital for Children in Indianapolis, IN.

Cassidy has a rare immunodeficiency and has been treated at Riley Hospital for Children since she was five months old. When Cassidy was six months old, she became very ill with croup. Within a matter of minutes of being triaged in the Riley Emergency Department, she stopped breathing on her own and was intubated and sedated for several days while doctors began to research a diagnosis and treatment plan. After several days, she was intubated. Her family says they were thankful for a diagnosis of croup at the time, this began our long journey of discovering the impact that a minor respiratory illness could have on Cassidy. After several years, her family discovered that she has a rare immunodeficiency with cold induced urticaria. Cassidy is now in kindergarten and thanks to a wonderful care team, she has avoided inpatient treatment since her hospital visit four years ago.

Thanks to donations to Children’s Miracle Network Hospitals, Cassidy has received lifelong support for her rare immunodeficiency condition.