Bio: Mindy Cameron brings over 17 years as a Duchenne advocate to her role as Patient Advocacy Lead at Santhera Pharmaceuticals. Mindy has served the DMD community in a wide array of capacities since 2004, when the youngest of her two sons was diagnosed with the disorder. She has worked closely with many Duchenne non-profit organizations over the past two decades, including CureDuchenne, Parent Project Muscular Dystrophy, and Little Hercules Foundation. In addition to her work with Santhera, Mindy is a member of the Patient Insights Board at Medidata Solutions, a global technology leader in the life sciences industry.
Mindy lives in Carmel, Indiana, where she serves as a board director for the Muscular Dystrophy Family Foundation and a member of the Carmel City Council’s Committee on Disability.