EPISODE HIGHLIGHTS Elizabeth Reynolds is a mom of three children and her oldest, William, has Pearson syndrome, a multi-system disease caused by a deletion in mitochondrial DNA. She is also […]
Expert Series: Ultra-Rare Mitochondrial Diseases: Development Challenges and Opportunities
Join CEO of Stealth Biotherapeutics Reenie McCarthy, and special guest Shelley Bowen, Director of Family Services and Advocacy for the Barth Syndrome Foundation, to discuss the health equity challenges faced […]
Energy in Action Podcast Episode 96: Employed with Mito Disease
EPISODE HIGHLIGHTS Tasia, can you tell us about yourself and the work you do? I’m 31 and I was diagnosed at a young age with fatty oxidation disorder. As a […]
Energy in Action Podcast Episode 94: Barth Syndrome – When the Lack of Fair, Equitable and Appropriate Regulatory Review Process Jeopardizes Ultra-Rare Drug Development
Barth Syndrome – When the Lack of Fair, Equitable and Appropriate Regulatory Review Process Jeopardizes Ultra-Rare Drug Development Barth Syndrome Foundation Executive Director Emily Milligan, and Director of Family Services […]
Expert Series: At the crossroad of mitochondrial disease and mitochondrial dysfunction
Why are patients with Fibromyalgia, Chronic Fatigue, Lymes diagnosed with mitochondrial disease? How do I know I have Mito? What should my doctor look for to consider further testing for […]
