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

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Sickle Cell Service Review 2018 – Findings from The Sickle Cell Society’s Engagement Activities

Between June and August 2018 we asked for your views about NHS England’s planned changes to short and long stay hospital admissions for people with Sickle Cell Disease. 

You can see our infographic and read the full report 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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