52 - Luisa Palazola and Rare Disease Day 2020

from The Spinal Muscular Atrophy Podcast with Kevin Schaefer · host SMA News Today

In episode 52, Kevin Schaefer talks with his coworker Luisa Palazola, a Community Manager for SMA News Today. Luisa is from Memphis, Tennessee, and she has another rare genetic condition called cystic fibrosis. During this conversation, she talks about her story and advocacy work, what she’s learned about SMA through her work here, and the upcoming event Rare Disease Day.

Episode metadata supplied by the publisher feed · Published Feb 18, 2020

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52 - Luisa Palazola and Rare Disease Day 2020

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This episode was published on February 18, 2020.

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