33^rd Annual Miracle Tournament and Celebration Dinner

Treated at UNM Children’s Hospital in Albuquerque, NM.

Natalie’s cancer journey began at the age of ten when her mom noticed her daughter’s visual impairment. She was diagnosed with an Optic Pathway Glioma, a type of cancer that is difficult to treat and can also affect the pituitary gland. After two chemotherapy sessions, the tumor had completely disappeared, and her family rejoiced. She continued chemotherapy for another year as neurologists monitored Natalie.

A few months later, an MRI identified an area of concern and a biopsy confirmed Anaplastic Astrocytoma, a different, more aggressive brain tumor. She immediately and courageously began treatment again, including 30 rounds of proton therapy radiation and 42 rounds of oral chemotherapy.

Although her treatment worked, she was left with hemiparesis, the weakness of her right side weakness, which required two years in physical and occupational therapy. Recently, an MRI detected a new area of concern, this time, in Natalie’s brain stem. To get a biopsy, Natalie needed major surgery to access the tumor through her cerebellum. Doctors found a Germinoma tumor and her family was relieved to learn that the condition is very treatable. Now, Natalie is bravely facing months of chemotherapy again at UNM Children’s Hospital.

Donations to Children’s Miracle Network Hospitals benefited Natalie’s highly tailored care throughout her journey.

Treated at Texas Children's Hospital in Houston, TX.

Kylea was born prematurely at 34 weeks in Kansas, and she tested positive for cystic fibrosis (CF). Her medical team thought it was a false positive since she had no symptoms. Months later, Kylea was still under five pounds. Her mom took her to the emergency center at a nearby children’s hospital in Missouri, where Kylea was admitted for jaundice. After a liver biopsy and other tests, including blood tests to look for the genetic mutations that cause CF, the family got confirmation: Kylea had two copies of delta F508, the most common genetic mutation that causes cystic fibrosis. Once she had an official diagnosis, Kylea’s family turned to Texas Children’s Hospital since they were ranked number one in pulmonology and offered a holistic approach to care. Her family moved to Houston, just in time for the new school year. Her childhood was filled to the brim with sports, dance, gymnastics, Girl Scouts, swimming, science camp, and trips to the zoo.

Today, she is 15 and studying French. She hopes to travel the world and study forensic psychology in college.

Thanks to donations to Children’s Miracle Network Hospitals, Kylea had access to world-class, holistic pulmonology care for cystic fibrosis.

Treated at Orlando Health Arnold Palmer Hospital for Children in Orlando, FL.

During their 20-week ultrasound, Akosua and Fernando learned that their baby had spina bifida. Determined to explore all options, they reached out to the Fetal Care Center at Orlando Health Winnie Palmer Hospital for Women and Babies after learning the hospital offered in-utero surgery for babies with this diagnosis. Within a week, Akosua started an evaluation to see if she and her baby were suitable for in-utero surgery, and thankfully, they were. At 25 weeks into her pregnancy, Akosua underwent surgery to correct the defect in Celeste’s spine. Seven weeks later, Celeste was born, weighing 4 pounds, 10 ounces. After a short stay in the neonatal intensive care unit to ensure her health, she was able to go home. Now, at five years old, Celeste is thriving. She walks on her own and enjoys gymnastics, swimming and playing with her sister. Celeste is smart, playful, determined and kind. Celeste goes to weekly physical therapy, and as she grows, she will continue to receive care at the Spina Bifida Clinic at Orlando Health Arnold Palmer Hospital for Children.

Donations to Children’s Miracle Network Hospitals helped fund the fetal surgery program and the state-of-the-art ultrasound machine used to detect spina bifida in kids like Celeste.