33^rd Annual Miracle Tournament and Celebration Dinner

Treated at Maria Fareri Children's Hospital in Hudson Valley, NY.

Camryn was diagnosed with Sickle Cell disease three weeks after birth. For most of her life, her disease had been managed. Four years ago, Camryn was diagnosed with Moyamoya disease (a narrowing of blood vessels in the brain). Her sickled blood cells would only complicate this condition. Camryn was in need of a stem cell transplant and her oldest sister, Skylar, was selected as her donor. Camryn was admitted to Maria Fareri Children’s Hospital and Skylar’s stem cells were harvested and transplanted into Camryn. It was inspiring for her family to witness this life-saving exchange among sisters! Camryn was hospitalized for 88 days and she found solace in the extraordinary care, and encouragement she received before, during and after her transplant. Today Camryn is feeling great and is an incredible advocate for the care she received at Maria Fareri Children’s Hospital.

Thanks to donations to Children’s Miracle Network Hospitals, Camryn received care and support as she underwent a stem cell transplant at Maria Fareri Children’s Hospital.

Treated at Nicklaus Children's Hospital in Miami, FL.

After a seemingly healthy pregnancy, Jaxon’s parents were told not to worry by medical providers by a few early signals that something seemed off. Thankfully, his uncle noticed the ridge along Jaxon’s forehead and did not believe the triangular shape of Jaxon’s head was caused by the trauma of delivery. At two weeks old, a CAT scan confirmed Jaxon’s metopic craniosynostosis, where the soft spot at the top of his head had been prematurely fused together in the womb. Jaxon’s parents took him to the renowned Nicklaus Children’s Hospital Brain Institute. At seven months old, Jaxon underwent an eight-hour cranial procedure at Nicklaus Children’s. Despite the challenges, he was in good hands, even combatting other anomalies such as the misalignment of the eyes, a hole in his heart, a horseshoe-shaped kidney, and more. Given the range of birth defects their son faced, Jaxon’s parents’ genetics testing at Nicklaus Children’s confirmed that he had a rare gene mutation in CDK13. There wasn’t much known about CDK13 at the time. Today, nearly 300 cases have been identified globally. For now, Jaxon’s parents treat each symptom as it arises. He struggles with tasks requiring the use of his hands and motor skills, and his ADHD and moderate autism made everyday life and academic tasks challenging. And yet, he continues to make remarkable progress in physical therapy, occupational therapy, and speech therapy. Jaxon’s resilience and carefree, fun personality positively inspires all the lives he touches.

Donations to Children’s Miracle Network Hospitals support the clinical institutes and personalized care that allow Jaxon to make remarkable progress on his journey.

Treated at UCSF Benioff Children's Hospitals in Oakland, CA.

Ripley was born with a congenital heart defect and spent the first week of his life in UCSF Benioff Children's Hospitals’ Intensive Care Nursery. A month later, he returned for open heart surgery to repair the defect, known as Tetralogy of Fallot, which reduces the heart’s ability to pump oxygenated blood to the body. He is part of a Cardiac MRI study at UCSF that is exploring the risks of brain injury in babies with congenital heart disease.

Thanks to donations to Children’s Miracle Network Hospitals, Ripley received access to critical care to correct his heart defect.