S3 E3 - One Family's Rare Disease Odyssey - CRELD1, Pt1

This week we come to you from the heart of Guys Hospital, London, supported by the South East Genomic Medicine Service Alliance. In the first part of this 2-part episode, Helen talks to Adam Clatworthy about his family's diagnostic odyssey that eventually saw 2 of his children diagnosed with the rare disease, CRELD1. Sharing the reality of their journey and daily experiences, we get an insight into the search for a diagnosis.