The Sickle Cell Society supports and represents people affected by sickle cell disorder to improve their overall quality of life.

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40th Anniversary Gala Ball

Celebrating 40 Years

The Sickle Cell Society is turning 40! To celebrate our 40th year we are running a whole host of events and activities. We would love for you to celebrate with us and get involved.

We have created a page dedicated to all our celebrations so you can see what we are up to, how to get involved and find out how to sign up to regular up-dates. 

Click here to find our more 

South London Gives

South London Gives is our project supporting people of African and Caribbean heritage to donate blood. More donors are urgently needed to support treatments for people with sickle cell that save and improve lives. Regardless of where you live in England, you can Register to be a blood donor here 

Find out more about South London Gives here

Paediatric Standards

New Updated Edition of ‘Sickle Cell Disease in Childhood: Standards and Recommendations for Clinical Care’

The 3rd edition of the paediatric standards has just been published to support paediatricians, haematologists, specialist nurses and psychologists, and those responsible for monitoring outcomes i.e. hospital trusts, commissioning authorities and peer-review services.

Download here:

The Sickle Cell Society believes that individuals with sickle cell disorder have 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…

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