Screening for sickle cell and beta thalassaemia

Overview

In this section you can find out about the experience of antenatal and newborn screening for sickle cell, beta thalassaemia and other haemoglobin variants, by listening to people share their personal stories on film. Our researchers travelled all around the UK to talk to 39 people in their own homes. Find out what people said about issues such as partner screening, telling people you’re a carrier, living with sickle cell and sources of support. We hope you find the information helpful and reassuring.
 
Interviews in other languages, Urdu: Interview 22, 30, Mirpuri: Interview 21, 24, Sylheti: Interview 16, Français: Interview 14, 18, 20, Português: Interview 25.
 
You can start viewing topics by clicking 'Next Topic' above, or selecting from the list on the left. You can also view 'People's Profiles' from the tab above.
 


Supported by:
Hulme University Fund, Oxford
NHS National Screening Programme for Sickle Cell and Thalassaemia
Programme Director Dr Allison Streetly

Publication date: October 2006
Last updated: September 2015
Review date: September 2017

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