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Sisällön tarjoaa USC Price and USC Sol Price School of Public Policy. USC Price and USC Sol Price School of Public Policy tai sen podcast-alustan kumppani lataa ja toimittaa kaiken podcast-sisällön, mukaan lukien jaksot, grafiikat ja podcast-kuvaukset. Jos uskot jonkun käyttävän tekijänoikeudella suojattua teostasi ilman lupaasi, voit seurata tässä https://fi.player.fm/legal kuvattua prosessia.
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A Professor’s Quest to Save Her Son

31:17
 
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Manage episode 415704271 series 3562920
Sisällön tarjoaa USC Price and USC Sol Price School of Public Policy. USC Price and USC Sol Price School of Public Policy tai sen podcast-alustan kumppani lataa ja toimittaa kaiken podcast-sisällön, mukaan lukien jaksot, grafiikat ja podcast-kuvaukset. Jos uskot jonkun käyttävän tekijänoikeudella suojattua teostasi ilman lupaasi, voit seurata tässä https://fi.player.fm/legal kuvattua prosessia.

Four years ago, Elizabeth Currid-Halkett received some of the worst news imaginable: her son, Eliot, was diagnosed with a fatal neuromuscular disease. In her quest to save her son, she learned of a gene therapy that ultimately helped Eliot, but she ran into roadblocks that made it difficult to access this life changing treatment. Her story, recently published in The New York Times, illustrates the obstacles that prevent some patients from obtaining rare disease treatments. In this episode, we are joined by Currid-Halkett, a USC Price School professor of public policy, and Alice Chen, an associate professor of public policy who recently testified before Congress about making rare disease treatments accessible.

  continue reading

9 jaksoa

Artwork
iconJaa
 
Manage episode 415704271 series 3562920
Sisällön tarjoaa USC Price and USC Sol Price School of Public Policy. USC Price and USC Sol Price School of Public Policy tai sen podcast-alustan kumppani lataa ja toimittaa kaiken podcast-sisällön, mukaan lukien jaksot, grafiikat ja podcast-kuvaukset. Jos uskot jonkun käyttävän tekijänoikeudella suojattua teostasi ilman lupaasi, voit seurata tässä https://fi.player.fm/legal kuvattua prosessia.

Four years ago, Elizabeth Currid-Halkett received some of the worst news imaginable: her son, Eliot, was diagnosed with a fatal neuromuscular disease. In her quest to save her son, she learned of a gene therapy that ultimately helped Eliot, but she ran into roadblocks that made it difficult to access this life changing treatment. Her story, recently published in The New York Times, illustrates the obstacles that prevent some patients from obtaining rare disease treatments. In this episode, we are joined by Currid-Halkett, a USC Price School professor of public policy, and Alice Chen, an associate professor of public policy who recently testified before Congress about making rare disease treatments accessible.

  continue reading

9 jaksoa

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