Join us each month to listen and learn from the experts – people living with rare conditions. We’ll
Jay joins David Rintell, Head of Patient Advocacy at BridgeBio to talk about his experience of livin
Dan joins David Rintell, Head of Patient Advocacy at BridgeBio to share the story of his long diagno
32 seconds. That’s how much time Brady could tolerate exposure to light on his skin before the onset
Anne and Mike continue their conversation with David Rintell, Head of Patient Advocacy at BridgeBio,
Anne joins David Rintell, Head of Patient Advocacy at BridgeBio to talk about how autosomal dominant
Lacey joins David Rintell, Head of Patient Advocacy at BridgeBio to talk about how LGMD2I/R9 has imp
Kristen joins David Rintell, Head of Patient Advocacy at BridgeBio to tell her personal story about
Veronica joins David Rintell, Head of Patient Advocacy at BridgeBio to tell her son Brent’s story. W
In part two of our series on ALS, amyotrophic lateral sclerosis, Holly and Beth, two women whose hus
Holly and Beth, two women whose husbands died from ALS, amyotrophic lateral sclerosis, (also known a
The birth of Jihan’s first daughter, Bella, was traumatic. She and her husband were totally unprepar
At birth, Jessica’s physician noticed she had low levels of calcium. Genetic testing later confirmed
In this month’s episode of On Rare, David Rintell speaks with Cliff and Noreen, the parents of Dyla
In this month’s episode of On Rare, David Rintell speaks with Alex, 18-year-old whose mother is livi
In this month’s episode of On Rare, David Rintell speaks with Erica, who is living with congenital a
Andrea and Ryan’s son, Parker, is living with tuberous sclerosis complex (TSC). During an ultrasound
Inês’ 9-year-old daughter, Clara, is living with achondroplasia. In this episode of On Rare, Inês de
In her 20s, Chaundra believed she was living the dream with a graduate degree and a new, exciting j
Brady is a five-year-old who is living with recessive dystrophic epidermolysis bullosa (RDEB), a rar
John and Tony are living with limb girdle muscular dystrophy type 2i (LGMD2i), a rare genetic condit
