Santi Beats the Odds: A Story of Perseverance


Patient Santino smiling.
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Patient of the Month: Naomi

June 30, 2025 – Diagnosed with scoliosis at six years old, Naomi has been fighting hard to prevent further curvature of her spine. After years of trying various treatment options, and with puberty causing greater curve progression, Naomi and her family sought other treatment options. It was at Nicklaus Children’s Orthopedic, Sports Medicine & Spine Institute where Naomi and her family found comfort and hope.

Caring for Matthew: Managing a Very Rare Disease

April 03, 2025 – Matthew was diagnosed with Phelan-McDermid Syndrome (PMS), a rare genetic disorder that affects development, speech, and cognitive ability, and requires extensive medical care and round-the-clock support. Despite his challenges, Matthew radiates love and joy, and his family is advocating for increased awareness of PMS while seeking potential treatments for the condition.

With Limb-Lengthening, Surgery Is Only the Beginning

March 11, 2025 – Liz, who was born with achondroplasia, had limb-lengthening surgery in January 2023 to help her gain more independence and improve her arm mobility. After months of therapy and adjustments, she reached her goal, giving her more freedom to do everyday activities without any limitations.

Optimal Care, Improved Life for Children With Spasticity

March 11, 2025 – Spasticity, which is often caused by brain or spinal cord injuries, is common in children with cerebral palsy and can result in muscle tightness, spasms, and problems like chronic constipation. The Nicklaus Children's Cerebral Palsy and Spasticity Program uses a team approach, offering both nonsurgical and surgical treatments to enhance the quality of life for kids, while providing personalized care and family support along the way.