Raremark | Rare Disease Community

Raremark | Rare disease community

Raremark Health

Learn About the Rare Disease Community: Meet Mara Gervais

Learn About the Rare Disease Community: Meet Leigh-Ana Rossitto

What does the rare disease community think about research?

Raremark Health

Learn About the Rare Disease Community: Meet Megan Loden and Chris Coates

Drug Development for Rare Diseases: A Community Conversation

National Organization for Rare Disorders (NORD)

Learn About the Rare Disease Community: Meet Dr. Dr. Harsha Rajasimha

Curing Rare Disease Is Possible | Lynn Hopkins | TEDxBelmontShore

Community in De Pere rallies to bring 12-year-old cancer patient home

NORD: 30 Years of Advocacy for the Rare Disease Community

National Organization for Rare Disorders (NORD)

10 Tips for Newly Diagnosed Rare Disease Patients and Families

National Organization for Rare Disorders (NORD)

Learn About the Rare Disease Community: Meet Deena Chisholm

Connecting Rare Disease Patient Communities and Advocacy Groups

What is Rare Disease Day?

National Organization for Rare Disorders (NORD)

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

Rare Disease Drug Development Education Series Trailer

National Organization for Rare Disorders (NORD)

Creating Community in Rare Disease

Advancing Health Equity: A Community Conversation for Rare Disease Day

National Organization for Rare Disorders (NORD)

The Misnomer of Rare [Disease] | Michelle Berg | TEDxFargo

Building a Community Engagement Model for Rare Disease: A Community Ambassador Approach

Rare Diseases Clinical Research Network (RDCRN)