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EPISODE · Sep 4, 2019 · 25 MIN

Susannah Cahalan and her Month of Madness

from RARECast

Journalist and best-selling author Susannah Cahalan, ahead of her keynote address at the Global Genes’ RARE Patient Advocacy Summit September 18 in San Diego, discusses about her diagnostic odyssey, the critical role the support of her loved ones made, and what allowed the doctor who diagnosed and treated her to succeed where others had failed.

Episode metadata supplied by the publisher feed · Published Sep 4, 2019

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Susannah Cahalan and her Month of Madness

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