16.8 Genomics and Stillbirth: What midwives need to know and why it matters

Stillbirth is a deeply challenging outcome of pregnancy, and families often look to their midwives for answers and support. In this session, we’ll explore where genomic testing is becoming a valuable tool in understanding the causes of stillbirth—and where its limitations lie. Through an illustrative case study and discussion of real-world pathways, we’ll highlight how midwives can play a key role in communicating genomic information, supporting informed decisions, and guiding families with empathy and clarity.Hosted by:Sue Macdonald, Midwifery Expert; Host and Curator, Maternity and Midwifery Festivals/Midwifery Hour, Editor, Mayes MidwiferyContribution from:Tina Prendeville , Lead Midwife, North Thames Genomic Medicine Service Alliance and Senior Research Midwife, Imperial College LondonDenise Barnes , Lead Midwife for Genomics, North East & Yorkshire Genomic Medicine Service AllianceEmma Tomlinson, Specialist Rainbow Clinic Midwife, Tommy’sSupported by MATFLIX: ⁠https://matflix.co.uk⁠Register to watch the next episode LIVE or attend a Maternity & Midwifery Festival: ⁠https://mmf.eventbrite.com⁠Watch the live stream: ⁠https://facebook.com/midwiferyforum/live