• It's Time for Heath Care

    The NHS Sickle Cell and Thalassaemia (SCT) screening programme is a genetic screening programme. This means that it also identifies people who are genetic carriers for sickle cell, thalassaemia and other haemoglobin disorders.

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    It's Time for Heath Care
  • Sickle cell and thalassaemia screening

    The NHS Sickle Cell and Thalassaemia (SCT) screening programme is a genetic screening programme. This means that it also identifies people who are genetic carriers for sickle cell, thalassaemia and other haemoglobin disorders.

    Read More
    Sickle cell and thalassaemia screening
  • Standards and Publications

    Access the latest clinical standards and guidelines

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    Standards and Publications

Sickle Cell Publications

Access all the Sickle Cell Societies research reports for healthcare professionals.
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SCORE

Sickle Cell Cohort Research transforming the lives of communities living with SCD in Nigeria.
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UKTS Care Standards

Standards for the Clinical Care of Children and Adults with Thalassaemia in the UK.
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Specialised service review

Haemoglobinopathies service review, conversations with colleagues. Find the nearest venue in January.
Find Venue

ASH Pocket Guides

A series of brief evidence-based pocket guides to help provide quality care to patients.
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New In Paperback

Genetics & Global Public Health: Sickle Call & Thalassaemia edited by S. Dyson and K.Atkin.
Order from Amazon

Forum Publications

Latest clinical standards, guidelines current and previous meeting presentations.
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Transcranial Scanning

Latest Transcranial Doppler standards.
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West Midlands Quality Review Service is a collaborative venture by NHS organisations in the West Midlands to improve the quality of health services by undertaking reviews of the quality of clinical services.
The National Haemoglobinopathy Registry is a database of patients with red cell disorders living in the UK. This new database collects data,which is required by the Department of Health from Haemoglobinopathy centres. The central aim of the registry is to improve patient care.
The National Institute for Health and Care Excellence (NICE) provides national guidance and advice to improve health and social care. Our guidance, advice, quality standards and information services for health, public health and social care. Also contains resources to help maximise use of evidence and guidance.
This Clinical Reference Group (CRG) covers Sickle Cell Disease (SCD), Thalassaemia and other very rare anaemias requiring lifelong transfusion and chelation. Haemoglobinopathies are complex disorders which although often grouped together and managed by the same specialist team, have distinct clinical manifestations and treatments.