Jett Foundation’s Podcast
Jett Foundation’s podcast will bring you recordings of our educational Awareness Days and more. These educational events serve people and families in the Duchenne muscular dystrophy community along with Jett Foundation’s many other programs and resources. We encourage you to give these podcasts a listen in order to learn more about Duchenne, how to better prepare for unexpected moments, help assist someone that relies on your support, and more.
Listen on:
Episodes
Wednesday Oct 11, 2023
Wednesday Oct 11, 2023
On February 28, 2023, we celebrated our 6th annual Rare Disease Day event with a presentation and panel discussion focused on anxiety and mental health in Duchenne.
Tuesday Oct 10, 2023
Tuesday Oct 10, 2023
The Two Disabled Dudes moderate on the ways the Duchenne and rare disease communities are breaking barriers in access to care and as we identify areas that still need improvement.
www.jettfoundation.org/wdad/
Monday May 22, 2023
Monday May 22, 2023
Jett Foundation hosted its 5th annual Rare Disease Day Event in a virtual setting with rare disease advocates, Duchenne community speakers, and individuals sharing their stories and advice for life with a rare disease.
This event was originally hosted live via Zoom on February 28, 2022.
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