Meet Molly, one of our Genomics Ambassadors
‘5 years ago, I would never have considered genomics an essential part of my job as a midwife. Now I see how important it is.’
After beginning her midwifery career in Australia, Molly moved to the UK to pursue a MSc in Women’s and Children’s Health. Her journey into genomics began more recently, when she started working as a research midwife on an exciting national research programme, called Generation Study.
‘Genomics has been more of a conversation for me over here in the UK, but newborn genomics programmes have been evolving over in Australia and around the world too.’
The Generation Study aims to help the NHS diagnose genetic conditions by screening 100,000 newborn babies for over 200 childhood-onset rare diseases. Molly was instrumental in setting up the study at one of the first hospitals in England, shaping how best to recruit women and birthing people to it.
Her role in the study now involves talking to families during pregnancy to introduce the study, tell them what to expect and to explain how genetic screening works. She also explores the processes that take place when a condition is suspected and what support is available for mothers and families should they need it.
‘I enjoy the back-and-forth conversations about genomics, healthcare and data. They are fruitful conversations that allow families to make informed choices and it’s so lovely when something positive comes out of it.’
‘It’s these interactions I have with families that are important to me. They make me question and explore things for myself.’
Molly shared her top tips for other healthcare professionals to consider when having genomic conversations with families.
‘Using approachable language, giving them the sufficient time to consider information, and providing resources that they can take away and process on their own, can help families to come to an informed decision. Especially when pregnancy poses a unique situation in life and they have to decide on behalf of their unborn baby.’
Over a year into the study, and those who have had a condition suspected result have been able to access specialist pathways and diagnostic testing. This allows them to engage with treatment earlier to help achieve better outcomes for their children. Negative screening results also provides mothers and families with confidence and reassurance.
As her passion for genomics continues to grow, Molly is currently completing her post graduate certification in Genomic Medicine at City St George’s University. She studies alongside a diverse group of healthcare professionals such as nurses, consultants, scientists and geneticists.
‘It’s nice to see genomics pulling so many professions together.’
She shared some advice for others who may be at the beginning of their genomics journey or looking to start.
‘As a midwife, it can feel overwhelming to begin with as you might not have had much training on genomics at university. But there are heaps of resources to engage with and more coming out all the time.’
Molly emphasised the importance for healthcare professionals to actively engage in conversations to help them improve their genomic literacy.
‘I think speaking about genomics with families and colleagues is really important to help us all wrap our heads around the subject and understand how enormously it will impact day to day healthcare.’
Looking forward, Molly is excited to see where her new passion will take her. As genomic research continues to advance, she is eager to be a part of what comes next.
