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“Data Silence” Holds High Stakes for People’s Health

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Manage episode 481648696 series 2463238
Content provided by The Commonwealth Fund. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by The Commonwealth Fund or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://ppacc.player.fm/legal.

We’re in a pivotal moment for health care equity and public health. Systems for tracking data on maternal mortality and chronic disease are being dismantled, with consequences that could last generations.

On this week’s episode of The Dose, Dr. Marcella Nunez-Smith joins host Joel Bervell to talk about who’s represented in the health data we collect, and who isn’t, and why it’s so important for “people to feel safe in sharing” their data and “to have trust that it’s protected.” Dr. Nunez-Smith also explains how her experience as a parent of a child with a rare disease frames how she approaches her work in health equity.

  continue reading

107 episodes

Artwork
iconShare
 
Manage episode 481648696 series 2463238
Content provided by The Commonwealth Fund. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by The Commonwealth Fund or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://ppacc.player.fm/legal.

We’re in a pivotal moment for health care equity and public health. Systems for tracking data on maternal mortality and chronic disease are being dismantled, with consequences that could last generations.

On this week’s episode of The Dose, Dr. Marcella Nunez-Smith joins host Joel Bervell to talk about who’s represented in the health data we collect, and who isn’t, and why it’s so important for “people to feel safe in sharing” their data and “to have trust that it’s protected.” Dr. Nunez-Smith also explains how her experience as a parent of a child with a rare disease frames how she approaches her work in health equity.

  continue reading

107 episodes

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