For Professionals – News

Dafydd’s story – Rare Disease Day 2021

Louise Wilkinson – Rare Disease Advocate and Genomics Partnership Wales Patient and Public Sounding Board Member – shares her family’s personal experiences of her son Dafydd’s rare condition and diagnosis through genomic testing.  Dafydd – One in a Million Dafydd was a happy smiley baby and despite a difficult birth (born 2 weeks early by… Read more »