All episodes
How One Everyday Superhero Combats Rare Disease
Terminally Ill Patients Find Hope in Utah's Right to Try Law
Discovering the Creative Use of Outrage
New Diagnostic Offers Fast Answers For Group of Rare Diseases
One Researcher's Effort to Address a Fundamental Challenge in Rare Disease Research
Turning Lights and Camera into Action: A Mom's Search for Answers
A Teenager's Transformation from Patient to Advocate
How the Orphan Drug Act Reshaped the Rare Disease Landscape
Why the OPEN ACT Could Greatly Expand Treatments for Rare Disease
Rare Disease Company Seeks 100 Drugs in 10 Years
A Run Across America to Raise Rare Disease Awareness
Tapping the Public to Keep Scientists Current on Rare Disease Research
Why Raising Awareness Matters in the Fight Against Rare Diseases
The First Lady's Date who Embodied Precision Medicine
Startup with NIH Deal Seeks to Speed Drugs for Rare Diseases
Expanding the Potential of Crowdfunding
A Father's Search to Cure His Son's Rare Disease
How Venture Philanthropy Can Accelerate Drug Development
How New Funding Models Are Accelerating Drug Development