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 Midwifery

Contribution from:

Tina Prendeville , Lead Midwife, North Thames Genomic Medicine Service Alliance and Senior Research Midwife, Imperial College London

Denise Barnes , Lead Midwife for Genomics, North East & Yorkshire Genomic Medicine Service Alliance

Emma Tomlinson, Specialist Rainbow Clinic Midwife, Tommy’s

Supported by MATFLIX: ⁠https://matflix.co.uk⁠

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