When a rare genetic disorder hits home, it takes someone like this week’s Team Never Quit Podcast guest, Stephanie Herzog, to help find strategies to cure it. The Duchenne Muscular Dystrophy (DMD) diagnosis of her son, Max, was the driving force to connect her with Cure Rare Disease, who is currently developing life-saving therapeutics in collaboration with the world’s leading academics, clinicians, regulatory experts, translational experts, and manufacturing experts. Stephanie serves as a board member. The organization’s ground-breaking research is bringing to fruition the potential for permanent muscular regeneration, which was, at one time, science fiction.