Between 2014 and 2017 Marie Coughlin was the lead officer for the Merseyside Cancer Screening Plan. She shares how she helped raise awareness of screening, particularly within vulnerable and hard to reach groups.
More than 400 delegates attended 8 training events across England ahead of the an evaluative rollout of non-invasive prenatal testing (NIPT) to the fetal anomaly screening pathway.
Book your place now on a screening masterclasses this autumn.
Princess Royal University Hospital, in Kent, has made a very simple change that is having a big impact on improving early access to sickle cell and thalassaemia screening.
The 2018 AAA screening national networking and information sharing day brought together more than 100 delegates from local providers, commissioners and the screening quality assurance service.
We are delighted to announce registration details for 2 upcoming national NHS Diabetic Eye Screening Programme events.
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.
My name is Nichola Goddard and in this blog I'd like to tell you about a regional DES networking day I attended and why I would encourage others to attend one in their region if they get the chance.
One of the questions health professionals regularly ask us via our screening helpdesk is ‘to whom and when can screening for Down’s, Edwards’ and Patau’s syndromes be offered?’
Sonia Segalini, a screening quality assurance project officer at Public Health England, explains how she overcame her fear of presenting.