Episode #19 - Infantile Spasms: Know the Signs and Take Action featuring Amy Miller

Share
Subscribe

Infantile spasms, also known as West Syndrome, is a rare and particularly severe epilepsy syndrome that typically begins within the first year of life. Identifying, diagnosing, and treating infantile spasms is critical to preventing cognitive and developmental delay. Sadly, many primary care doctors and parents alike are not familiar with the signs and symptoms of infantile spasms.

Amy Brin Miller, Executive Director of the Child Neurology Foundation, discusses how to tell if a baby is having spasms, steps parents should take if they suspect their child has infantile spasms, and why early intervention is critical.

Learn more about the challenges of identifying and diagnosing infantile spasms by watching this free webinar recording or viewing our FAQ.

 

Download Audio

Want to download this episode? Fill out the form below and enjoy the podcast any time you’d like!

    Back to Episode Download PDF

    Infantile Spasms Transcript

    Related Episodes

    featured episode
    ResearchTypes of Epilepsy
    August 7, 2024

    #140 Post-Traumatic Epilepsy: What We Know and Where the Research is Going

    Guest: Dr. Elisa Zanier

    Dr. Elisa Zanier of the Mario Negri Institute in Milan, Italy discusses the current state of research into Post-Traumatic Epilepsy (PTE).

    featured episode
    ResearchTypes of Epilepsy
    July 3, 2024

    #139 The NORSE Institute: A Mother’s Loss Drives Awareness and Research into a Devastating Form of Epilepsy

    Guest: Nora Wong

    After losing her son to a sudden and devastating form of epilepsy, Nora Wong founded the NORSE Institute to raise awareness and fund research.

    featured episode
    Living with EpilepsyTypes of Epilepsy
    December 27, 2023

    #132 Rare Epilepsy Organizations: Fostering Community and Advancing Research

    Guest: Dr. Justin West and Liz Ramirez

    This week on Seizing Life® we speak with two rare epilepsy organizations, The KCNT1 Epilepsy Foundation and The Cute Syndrome Foundation, about community, awareness, and advancing research.