Published May 12, 2025
Resource Library
Published February 26, 2025
Keepin’ It Rare: Let’s Talk Therapy with Dr. Al Freedman
Hear patients, caregivers and advocates discuss the mental health impacts of rare diseases in this 5-part video series.
Published November 15, 2024
Rare Disease Advisory Council 2024 Stakeholder Webinar Recording
The National Organization for Rare Disorders (NORD®) hosted this webinar for advocates interested in establishing Rare Disease Advisory Councils in every U.S. state. With the support of NORD, other patient organizations and stakeholders in the rare disease community, RDACs are enabling states to strategically identify and address barriers that prevent individuals living with rare diseases from obtaining proper treatment and care for their condition.
Published July 15, 2024
¿Por qué debería hacerme pruebas genéticas incluso si tengo un diagnóstico? [Infographic]
Published July 15, 2024
Why Should I Get Genetic Testing If I Already Have a Diagnosis? [Infographic]
Published April 29, 2024
National Volunteer Month Webinar
Published November 21, 2023
Medicaid Unwinding
Published January 27, 2023
Pruebas Genéticas Para Enfermedades Poco Comunes Y No Diagnosticadas
Published January 27, 2023
Genetic Testing for Rare and Undiagnosed Diseases
Published November 2, 2023
¿Qué son las Pruebas Genéticas?
Published November 2, 2023
Genetic Testing for Rare Diseases
Published October 11, 2023