In this episode, we explore the fascinating field of genomics and genetic testing. Join us as Kelly Kohut, lead consultant genetic counsellor, breaks down what genomics is and how it plays a crucial role in cancer care today. We also hear from Emma Jenkins, patient representative working with the Southeast NHS Genomic Medicine Service, who shares her personal journey with genetic testing. Emma candidly discusses her experience of being diagnosed with Lynch syndrome, a hereditary condition that increases the risk of developing certain cancers, following a family member's cancer diagnosis. This conversation offers valuable insights into the real-world implications of genomics and the impact of genetic testing on individuals and families. 

Content warning: This episode contains conversations about lived experience of cancer which you may find upsetting or triggering. Listener discretion is advised.  
 
Links from the episode: 
Lynch Choices- Website 
Macmillan Genomics Toolkit 

Resources to share with the people you support
Find links below to Macmillan's resources about genomics for people affected by cancer:
Cancer genomics


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If you work in health or social care, visit www.macmillan.org.uk/learning or Macmillan’s Learning Hub for more information about free education and training from Macmillan Cancer Support.

Disclaimer: The content and information in these episodes is for informational and educational purposes only and does not constitute medical advice. All examples discussed in episodes are UK based and reflect UK health systems at the time of recording. No material within this series is intended to be a substitute for professional medical advice, diagnosis or treatment. Always seek the advice of your physician or other qualified and registered healthcare providers.