Denise Morrow

Patient advocate and founder/CEO of Genetics for Health whose personal diagnostic odyssey led to the discovery of a primary CoQ10 deficiency via whole genome sequencing; now helps others interpret genetic data to find root causes of rare diseases.

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Mar 7, 2025 • 35min

Cracking the Code of Rare Diseases: Denise Morrow’s Genetic Discovery | Ep2

In this engaging conversation, Denise Morrow, a patient advocate and the founder of Genetics for Health, shares her remarkable journey from suffering with undiagnosed health issues to discovering a primary CoQ10 deficiency through whole genome sequencing. She discusses the transformative power of genetic data in unveiling rare diseases and her mission to empower others with similar experiences. Together with Dr. Karen Erbs, Denise aims to bridge patient-led genomic insights with clinical practice, making personalized medicine accessible for all.

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