Join us for this ONLINE event on Rare Disease Day 2023, find out about how rare genetic conditions, like SRS, are diagnosed and hear about what it’s like to live with Silver-Russell syndrome (SRS).

Featuring

• Gracie Taylor, Patient Voice (& Science Insights Alumni)
• Prof Mary Porteous, SE Scotland Rare Disease Diagnostic Service
• Dr Emma Wakeling, Clinical Genetics and Genomics Consultant, Great Ormond Street Hospital  & Medical Advisor to Child Growth Foundation
• Jeff Bolton, Chair, Child Growth Foundation