Rare Bootcamp: Empowering Rare Disease Warriors for the Battle

Access to Health Care: The North Carolina Newborn Screening Story

Living by Design: Amanda's Wilson Disease Story

Life with TIO: Ann’s Story

Gene Therapy: What Does It Mean for Rare Disease Communities?

LC-FAOD: A Global Community

Life with LC-FAOD: Tasia’s Story

Managing FAOD Together: Michelle and Jake’s Story

Regina: Rare Strength in Caring

Life with GSDIa: Jonah’s Story

Life with Osteogenesis Imperfecta: Cindy and Matthew’s Story

Going beyond for Mason | Angelman syndrome (AS) (Full-Length Video)

Going beyond for Levi | Duchenne muscular dystrophy (DMD) (Full-Length Video)

Life with XLH: Cheryl’s Story

Going beyond for Levi | Duchenne muscular dystrophy (DMD)

Going beyond for Mason | Angelman syndrome (AS)

Ultragenyx is building a gene therapy plant

Built to Be Rare

Quick Tip Caring for Yourself While Caring for Others

Ultragenyx: Built to be Rare

I'm Rare at Ultragenyx

Ultraimpact

Ultrafocused