How Mitochondrial Research Moves Forward: From Patient Experience to Scientific Discovery
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Every breakthrough in mitochondrial disease research starts the same way – with a patient's voice. This episode traces that full journey: how listening to patients shapes the questions researchers ask, how natural history studies build the foundation for understanding a disease, and how that knowledge translates into clinical trials designed to test real therapies. Along the way, we'll explore why this only works when patients, clinicians, researchers, advocacy organizations, and industry all row in the same direction – and why that collaboration is what ultimately accelerates the path to treatments and cures.
Featuring
• Philip Yeske, PhD, Science & Alliance Officer, United Mitochondrial Disease Foundation
• Kristie Cline, Head of Patient Advocacy, Pharming
• Magnus Hansson, MD, PhD-VP and Clinical Development Head for Mitochondrial Disease, Pharming
• Danielle Black, MPH, Clinical Research Coordinator, United Mitochondrial Disease Foundation