In the Rare Journeys hub, discover stories from people in the rare disease community.

Explore all of the stories across AADC deficiency (AADCd), Duchenne, Friedreich ataxia (FA), Huntington’s disease (HD), phenylketonuria (PKU), or spinal muscular atrophy (SMA), or choose stories from a specific condition using the “sort by” button. Click on the tile to read the story.