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Podcasts

Listen to Episode #26 Wolfram Syndrome Expertise from Dr. Fumihiko Urano from the Podcast “It Happened to Me”

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December 20, 2023/by The Snow Foundation
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Podcasts

Listen to Episode #18 Hattersley-Urano Wolfram Syndrome with Parent Tamara Blum from the Podcast “It Happened to Me”

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September 12, 2023/by The Snow Foundation
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Podcasts

Listen to Episode #5 Wolfram Syndrome with Dr. Sarah Gladstone from the Podcast “It Happened to Me”

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March 3, 2023/by The Snow Foundation
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Podcasts

Listen to Episode #3 Wolfram Syndrome with Cathy Gildenhorn from the Podcast “It Happened to Me”

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March 3, 2023/by The Snow Foundation
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The Snow Foundation is a collective voice for Wolfram syndrome patients, working towards a cure for Wolfram syndrome and developing novel therapies for diabetes, vision loss, hearing loss and neurodegeneration.

Rare Diseases…Common Problems

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