33^rd Annual Miracle Tournament and Celebration Dinner

Treated at Corewell Health Children's in Detroit, MI.

Ages 12 & 10

Braylen was born weighing two pounds and one ounce. Since he was a premature baby, by the time he turned three, he was diagnosed with severe receptive and expressive language delay. His communication difficulties made it hard for him to connect with his peers. Braylen began receiving speech therapy through Corewell Health Children’s and was enrolled in the RE/MAX Communication Preschool Program to learn in a school-based environment where children are free of judgment. Through various therapies and the preschool curriculum, Braylen gradually began finding his voice and expanding his ability to connect with others. His mom says, “the greatest joy is that he is now able to better communicate not only with family but his peers. Each step forward, no matter how small, is a testament to his determination and unwavering spirit.”

Donations to Children’s Miracle Network Hospitals helped Braylen receive the therapy he needed to communicate with his peers and family.

Rylee lights up a room with her radiant energy. At four years old, she was diagnosed with severe mixed receptive and expressive language disorder and started receiving speech services at Corewell Health Children’s RE/MAX Communication Preschool Program. Despite her struggles with language, Rylee’s intelligence shines through. With the support of her family, speech therapists, preschool educators, and her Corewell Health Children’s Miracle Network Hospitals team, Rylee made remarkable strides in overcoming the challenges posed by her language disorder. Today, Rylee’s keen sense of creativity and ability to think outside the box matches her determination and strong spirit. She understands firsthand the frustrations of struggling to be heard and understood, and thus, she has become a fierce advocate not only for her own needs but for others as well.

Thanks to donations to Children’s Miracle Network Hospitals, Rylee is able to use her words to communicate and advocate for others with shared experiences.

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 Children's Health Foundation in Oklahoma City, OK.

At a routine 18-week ultrasound, Connor was diagnosed with the most severe form of spina bifida and hydrocephalus. His family met with the neurosurgery team at Oklahoma Children’s Hospital in Oklahoma City to learn how to prepare for Connor’s care after birth. He was born at 36 weeks and was immediately taken to the neonatal intensive care unit (NICU), where he stayed for 10 days. His first surgery was at two days old to close the hole in his back to protect his exposed spinal cord. Then, three days later he had brain surgery to place a shunt to drain the fluid in his brain (hydrocephalus). Just before he turned two, he began having long, life-threatening seizures. The seizures have caused Connor to have speech and cognitive delays. Connor receives occupational, physical and speech therapies to help with his development. Over the last 12 years, Connor has had 26 surgeries. Connor has paralysis in his lower half and has required multiple orthopedic surgeries in the last few years to correct his scoliosis, hip dysplasia, and some broken bones caused by low bone density. He loves watching sports, swimming, and watching his big sister dance. He enjoys playing adaptive baseball and attending Wheelie Club, an all-abilities club of varying activities.

Donations to Children’s Miracle Network Hospitals helped Connor receive life-saving care in the NICU and through his numerous surgeries.