40 min listen
Part One: Community Stories of Navigating a Rare Epilepsy Diagnosis
FromBrain & Life
ratings:
Length:
48 minutes
Released:
Jul 6, 2023
Format:
Podcast episode
Description
This week, in the first of two episodes, Dr. Daniel Correa speaks with families who share how SYNGAP1—a rare genetic neurologic disease that causes seizures and developmental delays—has impacted their loved ones and how SynGAP Research Fund (SRF) provides them with resources and community. Dr. Correa also speaks with Dr. Angel Aledo-Serrano, a neurologist and director at Vithas Madrid Neuroscience Institute. Dr. Aledo-Serrano explains SYNGAP1, when individuals should consider seeking genetic testing, and how it relates to other genetic neurologic conditions. Additional Resources SynGAP Research Fund (SRF) Brain & Life: How Parents Advocate for Their Children with Rare Diseases Learn more about autism spectrum disorder Learn more about epilepsy American Epilepsy Society (AES) We want to hear from you! Have a question or want to hear a topic featured on the Brain & Life Podcast? Record a voicemail at 612-928-6206 Email us at BLpodcast@brainandlife.org Social Media: Guest: SynGAP Research Fund @cureSYNGAP1 (Twitter); Dr. Angel Aledo-Serrano @AledoNeuro (Twitter) @aledoneuro (Instagram) Host: Dr. Daniel Correa @neurodrcorrea
Released:
Jul 6, 2023
Format:
Podcast episode
Titles in the series (100)
Susannah Cahalan on Anti-NMDA Encephalitis and Her Journey to Diagnosis: Susannah Cahalan on Anti-NMDA Encephalitis and Her Journey to Diagnosis by Brain & Life