Parents' Stories and Service Evaluation in Antenatal Screening

Parents' Stories and Service Evaluation in Antenatal Screening

By Sickle Cell Society

Date and time

Wednesday, March 21, 2018 · 10:30am - 3:30pm GMT

Location

Unique Venues Birmingham

6 Centenary Square Broad Street Birmingham B1 2EP United Kingdom

Description

The Sickle Cell Society and the UK Thalassaemia Society in association with the NHS Sickle Cell and Thalassaemia Screening Programme present a free conference for all health professionals working in antenatal care and screening, service users of the screening programme and other stakeholders.

This conference chaired by Professor Dame Elizabeth Anionwu will discuss the results of a two year collaborative project between the NHS Screening Programme and the two patient Societies which investigated the causes of late offers of antenatal screening and prenatal diagnosis in couples at risk of having a child with sickle cell or thalassaemia. We will present the personal stories of women and couples who have recent experience of the NHS Sickle Cell and Thalassaemia Screening Programme as well as a clinical audit and service evaluation conducted as part of the work.

Understanding 'Parents' Stories' is essential if the Screening Programme is to build a service that meets user needs and meets the programme objectives. This work has already been used to inform new standards and guidelines and public and professional educational resources. The conference invites service providers and users of the Screening Programme to join us as we share the learning and recommendations from the project and discuss more ways to provide a screening service that more adequately meets the needs of the public for whom it was established.

Organized by

The Sickle Cell Society is the only national charity in the UK that supports and represents people affected by a sickle cell disorder to improve their overall quality of life. First set up as a registered charity in 1979, the Sickle Cell Society has been working alongside health care professionals, parents, and people living with sickle cell to raise awareness of the disorder. The Society’s aim is to support those living with sickle cell, empowering them to achieve their full potential. To find out more visit www.sicklecellsociety.org or on Twitter, Facebook or Instagram: @SickleCellUK

Sales Ended