GOV.UK
Find out what happened at our event about digital screening information for pregnant women
Read about our event for Trust screening co-ordinators as part of our work to move to digital antenatal and newborn screening information.
Liane Powell
Liane has worked in screening since 2013, firstly as an Antenatal and Newborn Screening Coordinator for a multi-site NHS Trust, then as Project Lead within the Fetal Anomaly Screening Programme.
She loves the variety and depth of the work within the Antenatal and Newborn Screening Programmes, and the rewards and challenges that working within PHE Screening brings.
She is a registered midwife and nurse and remains focussed on enabling high quality care for women and babies.
She lives near the Lake District and enjoys spending time exploring the Lakeland fells with her family, from their trusty campervan.
User research into antenatal and newborn digital screening information
We've been busy asking people for their views about the move to digital screening information. Find out more about the different ways we've been consulting with our users.
Antenatal ultrasound scan information sheets updated
We have updated and improved the national information we provide about the ultrasound scans offered to women during pregnancy.
New spina bifida and anencephaly information leaflets for parents published
Today, we have published updated parent information leaflets covering anencephaly and spina bifida, 2 of the conditions screened for at the fetal anomaly screening mid-pregnancy scan.
Updated information on congenital heart disease published for parents
Today, we have published the updated information fetal anomaly screening programme leaflet for parents about congenital heart disease.
A new home for NIPT training resource
An update for those who have been nominated to deliver non-invasive prenatal testing training within their organisation.
National fetal anomaly screening guidance updated
We have updated our national guidance the NHS Fetal Anomaly Screening Programme (FASP) handbook and the FASP handbook for laboratories to help ensure local screening services meet national standards.
We need your help to assess impact of NIPT cascade training
The NHS Fetal Anomaly Screening Programme wants to know how cascade training has impacted on the knowledge and confidence of participants who discuss the offer of screening for Down’s syndrome, Edwards’ syndrome and Patau’s syndrome with women.
We’re improving our information on fetal anomalies for parents
Today, we have published an updated version of our leaflet 'Congenital diaphragmatic hernia (CDH): information for parents'.
Hundreds have already attended new NIPT training
The NHS Fetal Anomaly Screening Programme is running a series of training events to help healthcare professionals support women in making personalised informed choices about screening for Down’s, Edwards’ and Patau’s syndromes.