Dr Julie Ann Man

Julie worked as a medical doctor in the NHS and undertook medical doctoral research in paediatric pathology at Great Ormond Street Hospital, London. 

When becoming a mother, Julie’s focus shifted towards prioritising family life, personal health and supporting her husband in his role as an anaesthetist.   

Julie and her family were immersed into the world of Genomics in 2025 when their youngest son was diagnosed with a rare genetic condition, White Sutton Syndrome. 

Julie is passionate about caring and advocating for others which was a driving factor in becoming a doctor. With an understanding of medicine, medical ethics and law, research and lived experience of a rare genetic condition, Julie brings a unique perspective to the Panel.