A Fathers Search For a Cure - Rare Genetic Di...

In this episode, I’m joined by Dr. Nirav Shah, a neurologist turned health tech innovator. Dr. Shah shares his incredible journey from stroke neurologist to founding a startup that transformed patient care with wearable tech. We dive into how he built software that integrates FDA ...  Show more

In this episode, I'm joined by Dr. Mohit Joshipura, the VP of Clinical Affairs at OpenLoop. Mohit shares his incredible journey from practicing internal medicine to becoming a key player in the digital health space. We dive deep into the world of clinical operations and what it t ...  Show more

Mapping the human genome led to big advances in diagnosing rare disease. But diagnosis is only the first step in dealing with an illness. So what do you do if your child is found to have a condition that has no treatment? We hear from Michelle Teng, a mother who co-founded a biot ...  Show more

There are neglected tropical diseases, and then there is Noma, a severe gangrenous disease which tends to affect 2 to 6-year-olds and has a 90% fatality rate. Its quick onset means that often children die before they can get medical attention and it is thought that many medical p ...  Show more

Biomedical researcher Sonia Vallabh's life was turned upside down when she learned she had the genetic mutation for a rare and fatal illness, prion disease, that could strike at any time. Thirteen years later, her search for a cure has led to new insights about how to catch and p ...  Show more

Esta semana, en el segundo de dos episodios, el Dr. Daniel Correa continúa la conversación de la semana pasada con las familias que comparten cómo SYNGAP1-una rara enfermedad neurológica genética que causa convulsiones y retrasos en el desarrollo-ha afectado a sus seres queridos. ...  Show more