Patient engagement and involvement in rare disease research

Commun Med (Lond). 2023 Feb 28;3(1):20. doi: 10.1038/s43856-023-00251-7.

Abstract

Megan O’Boyle is the parent of a 22-year-old daughter with a rare neurodevelopmental disease. She is currently the Patient Engagement Lead of the RARE-X Data Collection Program at Global Genes, a collaborative platform for global data sharing and analysis created to accelerate treatments for rare diseases. In this Q&A, we ask Megan a series of questions on patient engagement and involvement in rare disease research.

Publication types

  • Interview