• Living with Apert Syndrome: Xavier's Story

  • Apr 30 2025
  • Duración: 1 h y 6 m
  • Podcast

Living with Apert Syndrome: Xavier's Story

Escúchala gratis

Ver detalles del espectáculo

  • Resumen

  • In 2019, Katy Martins welcomed her fourth child, a son named Xavier. Shortly after his birth, Xavier was diagnosed with Apert Syndrome—a rare genetic condition that affects approximately 1 in every 65,000 to 88,000 live births. Today, Katy sits down with Tahnee to share their family’s journey. Tune in as we explore what Apert Syndrome is, how it affects those who live with it, and the strength and resilience behind their story.

    https://www.gosh.nhs.uk/conditions-and-treatments/conditions-we-treat/apert-syndrome/
    Más Menos
Más Menos
adbl_web_global_use_to_activate_webcro768_stickypopup

Lo que los oyentes dicen sobre Living with Apert Syndrome: Xavier's Story

Calificaciones medias de los clientes

Reseñas - Selecciona las pestañas a continuación para cambiar el origen de las reseñas.

Reseñas de Audible.com

Opiniones de Amazon
No hay comentarios disponibles