Welcome to the Sickle Cell Society Website     


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1 in 20 from risk groups carries a trait for Sickle Cell Disorder. The child of two carrier parents may inherit a full blown Sickle Cell Disorder. These disorders have no cure and will affect every aspect of the child's life. Before starting your family, a simple blood test can reveal if you're the one.

For more information contact the Sickle Cell Society on:
020 8961 7795

Sickle Cell Society

The Sickle Cell Society believes that every sickle cell sufferer has the right to quality care. This can only be achieved if funding is made available to educate health carers and other professionals about the condition. The Society aims to provide this.

The Society does not discriminate between the types of sickle cell disorders or the ethnic groups concerned. Both sexes are equally affected, and should have equal access to support and services in a confidential and sensitive environment.

We respect the views of every patient.




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What you can do:

Donate and help save lives

Latest Events



Package of Care proposal for Sickle Cell patients. Click here for details

Iron Monitoring and Managment in Sickle Cell Disease. Click here for details

FerriScan recommend for measuring liver iron concentrations in patients with sicklec cell disease. Click here for details



Sickle Cell Society

Contact Details

Sickle Cell Society
54 Station Road
London
NW10 4UA
United Kingdom

Tel: 020 8961 7795
Fax: 020 8961 8346

Email: info@ sicklecellsociety.org

Disclaimer

The Sickle Cell Society is a charitable organisation whose aims include giving the public information about sickle cell disorders. This website contains general information only. Nothing in it should be treated as advice on handling a particular case.

For that a doctor who is responsible for the medical care of the person concerned should be consulted. The Society cannot accept responsibility for mistakes or inaccuracies in the content of this website and opinions expressed in it are not necessarily those of the Society.

If you have questions please email info@sicklecellsociety.org

Design © 2009 Brigitte Clarke

© 2009 Sickle Cell Society Registered Charity (No. 1046631)