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Neurology

When 10-month-old Seandelle first arrived at Nemours Children’s Health, his future was uncertain. He had survived severe injuries, but from the beginning, his new mother saw something different, “He had a drive in him. I just knew I couldn’t walk away.” Over the next several years, Nemours Children’s specialists across neurology, rehabilitation, ophthalmology, and surgery worked closely together to support him. His mother says, “Every doctor treated him like he was their own. They stopped, listened, and went above and beyond.” By age 3, Seandelle began experiencing clusters of seizures, sometimes lasting up to 30 minutes. After many tests and hospital stays, his care team recommended a major procedure to disconnect one side of his brain. It was a terrifying decision. “It was the hardest choice of my life,” his mother shared. “I was scared.” Neurologist Dr. Lily Tran, MD, his  Pediatric Epileptologist, recommended that they proceed with epilepsy surgery […]

Isaac’s journey with Nemours Children’s Health began after a long search for answers.  Around his first birthday, his parents noticed that something wasn’t right. “Isaac was extremely nauseated, underweight, and falling behind developmentally,” his mom recalled. After months of uncertainty, genetic testing revealed a rare diagnosis: SYNGAP1, a condition that affects only about 475 people in the U.S. and roughly 1,500 worldwide. SYNGAP1 causes developmental delays, epilepsy, and autism, making even everyday milestones more difficult.  Before coming to Nemours Children’s, Isaac’s seizures were constant and resistant to medication. “His neurologist said it was as if his brain were on fire,” his mom said. “He would just sit and stare off into space most of the day.” At just 3 years old, SYNGAP1 has left Isaac fully disabled, and he is not yet walking or talking. The emotional and physical toll was heavy for his family, who had spent years visiting multiple hospitals and doctors without answers.  That changed when […]

Read Amais’s Story in English En enero de 2024, la familia de Amaia llevó a su hija de dos años a la sala de emergencias de Nemours Children’s Hospital, Florida, en Orlando, después de notar que tenía crisis de mirada fija. Las crisis de mirada fija son un tipo de epilepsia focal corta, durante la cual el niño presenta una mirada vacía, confusión o pérdida de la conciencia de su entorno, a menudo sin ningún síntoma perceptible.  Su madre, Stefanie, recuerda el día exacto: “Amaia comenzó a sangrar por la nariz y a comportarse de una manera que no era normal, como girar y mirar hacia su lado izquierdo de una manera muy fuerte y sin moverse, e incluso se puso de color morado. Por eso decidimos llevarla a la sala de emergencias de Nemours”. Esa visita reveló un descubrimiento que les cambió la vida: un tumor cerebral. El impacto […]

Lee la historia de a Amaia en español In January 2024, Amaia’s family brought their two-year-old daughter to the ER at Nemours Children’s Hospital in Florida after noticing staring seizures. Staring seizures are a type of short focal seizure, during which a child will stare blankly, confused or lose awareness of their surroundings, often without any noticeable symptoms.  Her mother Stefanie remembers the exact day: “Amaia started bleeding through her nose and was behaving in a way that was not her normal, such as turning/looking to her left side in a very strong way and not moving – even turning purple [blue]. Then we decided to take her to the ER at Nemours.” That visit revealed a life-changing discovery: a brain tumor. The impact was immediate. “The impact of this news on our lives was extremely strong. I had to stop working to care for Amaia, take her to the […]

Peter, a child with Down syndrome adopted from Hong Kong at the age of 3, has faced numerous health challenges throughout his life. His journey, including multiple surgeries and comprehensive care, is a testament to the importance of dedicated medical support. Peter’s health issues were first identified when his parents noticed he wasn’t thriving. After consulting several specialists, a podiatrist with training at Nemours Children’s referred them to Nemours Children’s Health. After several tests, Peter received a critical diagnosis: his C1-C2 vertebrae were not fused, posing a significant risk to his spinal cord. In September 2017, Peter underwent a lifesaving C1-C2 fusion surgery performed by Dr. William Mackenzie and Dr. Jeffrey Campbell at Nemours. Following the surgery, Peter showed remarkable improvements in various areas, including potty training, communication, and education. However, his journey was far from over as Peter was still experiencing complications with his foot. Further examinations with Dr. […]

As a young athlete, Erin had faced her share of injuries, requiring her to go through physical therapy (PT) several times. These transformative experiences that ignited a passion within her. “The care I received sparked a desire to help others regain their ability to participate in the sports and activities they love,” Erin reflects. Initially, she envisioned a career focused on pediatric rehabilitation, driven by her understanding of the challenges young athletes face. However, during her physical therapy schooling, a neurology rotation at the MS Comprehensive Care Center exposed her to world of neurologic rehabilitation.” I was drawn to the complexity and challenge of working with the neurologic population and discovered a passion for adaptive equipment,” says Erin. After graduating, Erin gained valuable experience in both acute care and outpatient settings. Her skills and knowledge grew with each patient she treated. A few years into her career, she was encouraged […]