National Volunteer Month Webinar

Genetic Testing for Rare and Undiagnosed Disorders

Rare Disease Day Rare Teen Parents Webinar

Francis Collins Teaser Trailer

Preview of FARA Interview

05 Overcoming Ableism While Parenting

08 A Mother's Story: How My Son's Life Inspired Me to Make a Difference

04 Transitioning from Childhood to Adulthood with Rare Disease

The 2022 Rare Impact Awards

01 From Bitter to Better: My Invisible Rare Disease

07 Rare Breakthroughs: Hope Now And On The Horizon

06 Rare Disease Onset and Diagnosis in Adulthood

03 Beyond Coping: Resiliency While Rare

02 Building and Quarterbacking Your Care Team

Rare Breakthroughs: Hope Now and on the Horizon

Closing Keynote: Dented, Not Broken

Beyond the Disability or Diagnosis: Rare Disease in Adulthood

Debunking the Myths of Palliative Care

Rare in the Family: Family Planning and Decision-making

Living with Uncertainty

Rare Breakthroughs: Hope Now and on the Horizon

General Session Introduction

Opening Keynote: Resilient and Rare

How to Participate in Rare Disease Research

2023 NORD Breakthrough Summit: "I Am Enough" by Casey McPherson

Rare Disease Drug Development Education Series Trailer

Involucrar a las comunidades latinas de enfermedades raras

Engaging Latino Rare Disease Communities: Lessons from NORD’s Latinos and Rare Program

NORD Rare Impact Awards | 2023

Abbey Meyers Accepts Lifetime Achievement Award