Episode 2 – On trial

Rare in Common: the podcast
28/02/2018 22 min
Episode 2 – On trial

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Episode Synopsis

When two of Jenn’s children were diagnosed with Duchenne Muscular Dystrophy (DMD), it changed her life. Since then, she’s fought for access to clinical trials and new treatments and inspired others to join the cause along the way.

More episodes of the podcast Rare in Common: the podcast

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Episode 28 – #RareDiseaseTruth: how a hashtag is changing the conversation this Rare Disease Day 25/02/2021
Episode 27 – “It’s working time”: building Sophie’s Neighborhood 30/07/2020
Episode 26 – From diagnosis to network director—living with XLH 25/06/2020
Episode 25 – What does COVID-19 mean for the rare disease community? 09/04/2020
Episode 24 – The promise of genetic testing in rare 26/03/2020
Episode 23 – Breaking through with interactive education in rare disease 27/02/2020
Episode 22 – Misdiagnosed: The importance of genetic testing 30/01/2020
Episode 21 – From broad questions to exact answers 19/12/2019
Episode 20 – Taking back life by tackling diagnosis 21/11/2019
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