Part 2-Gene Therapy: A Patient Advocate's Perspective episode artwork

EPISODE · Oct 29, 2020 · 27 MIN

Part 2-Gene Therapy: A Patient Advocate's Perspective

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Shortly after birth, Kim Nye’s first daughter Tessa began suffering seizures. Though Nye gave birth to other children without significant health issues, when her fourth child Colton was born, he had the same symptoms as his oldest sister. The two siblings were eventually diagnosed with an ultra-rare genetic disorder and Nye began the TESS Research Foundation. The organization has been pursuing a gene therapy, which a biopharmaceutical company is now working to develop. In this second part of our series on gene therapies, we spoke to Nye about her own journey to becoming a rare disease advocate, how a gene therapy fit into her organization’s research agenda, and the considerations she is weighing before dosing her children with an experimental gene therapy.

Episode metadata supplied by the publisher feed · Published Oct 29, 2020

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Kim Nye, founder and president of the TESS Research Foundation, discusses her own journey to becoming a rare disease advocate, how a gene therapy fit into her organization’s research agenda, and the considerations she is weighing before dosing her children with an experimental gene therapy.

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Part 2-Gene Therapy: A Patient Advocate's Perspective

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