El camino de Luigi hacia un futuro mejor


Luigi y familia
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Noticias Relacionadas

Cuidar de Matthew: El tratamiento de una enfermedad muy rara

abril 03, 2025 – A Matthew le diagnosticaron el síndrome de Phelan-McDermid (SPM), un raro trastorno genético que afecta al desarrollo, el habla y la capacidad cognitiva, y que requiere una amplia atención médica y apoyo permanente. A pesar de sus dificultades, Matthew irradia amor y alegría, y su familia aboga por una mayor concienciación sobre el SPM al tiempo que busca posibles tratamientos para esta enfermedad.

Lily Shines a Light on the Importance of Early Detection of Neuromotor Delays

marzo 12, 2025 – Lily, age 2 ½, is walking independently and making remarkable progress, thanks to rehabilitative intervention at Nicklaus Children’s Hospital and an early diagnosis of cerebral palsy.

Leading Pediatric Epilepsy Care for 40 Years

febrero 26, 2025 – For 40 years, Nicklaus Children's Hospital has been a leader in pediatric epilepsy. Learn more about the comprehensive care we offer for the most complex chronic cases.

Gene Therapy Offers New Hope for Children with Duchenne MD

enero 23, 2025 – At Nicklaus Children's Hospital, gene therapy offers a promising treatment that dramatically improves life for children with Duchenne muscular dystrophy. Recognizing the potential wielded by a new gene therapy, Nicklaus Children’s became one of the first in the nation to offer ELEVIDYS-dystrophin soon after the FDA's 2023 approval.