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Information and resources for health professionals who provide counselling for people at risk of having a baby with sickle cell disease or thalassaemia.
Information on accessing victim and witness support services.
Guidance for healthcare professionals covering the pathway for sickle cell and thalassaemia screening.
These leaflets, in English, French, Bengali and Urdu, can help healthcare professionals speak with people about sickle cell disease.
Use this letter to inform mothers about their carrier result, as well as invite the biological father for a blood test.
Salmonella infections are a common bacterial cause of invasive disease in people with sickle cell disease especially children
Forms for sickle cell and thalassaemia (SCT) screening laboratories to send antenatal data to the national programme.
A collection of the annual reports for Sickle cell and thalassaemia screening (SCT) standards from 2021/22 inclusive.
This document describes the sickle cell and thalassamia (SCT) screening pathways.
Guidance on using the sickle cell and thalassaemia (SCT) newborn outcomes solution web system.
This document sets out guidance for commissioning care services for people with sickle cell disease, thalassaemia and other haemoglobin conditions.
Information for parents of babies who carry the sickle cell gene.
Information about the SFPC programme to help safely reduce the number of children entering care.
Recommended process for contacting fathers-to-be to offer screening for sickle cell and thalassaemia.
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