Sickle Cell Society
Sickle Cell Society

Sickle Cell Society

6 months ago ·Translate ·Youtube

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… read more

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:


Online Fundraising

For many people, fundraising online is the easiest way to support the causes you love. We’ve created a range of great options which you can use to support our work. We have broken it down into three categories to help you make the best out of your fundraising.

Click link to find out more:


Sickle Cell and Coronavirus (COVID-19) Survey

If you live with sickle cell, or care for someone who does, please consider completing our short survey and help us research the impact of coronavirus:

The survey has been created as part of our work with the Sickle Cell and Thalassaemia All-Party Parliamentary Group.


Coronavirus (COVID-19) & Sickle Cell Disorder

As you have probably seen on the news, COVID-19 is a new illness that can affect your lungs and airways. It’s caused by a virus called coronavirus.

For guidance and advice about coronavirus and sickle cell view our guidance page: