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

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BECOME A MEMBER

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Business As Usual (Office Closure & Working from Home)

We will soon be closing our office again to carry out much needed improvements. These improvements will make our office a better work space, which is more accessible and will have more welcoming spaces for service users.

The office will be closed from Monday 17th May to Monday 26th July 2021.

Even though our office is closed, business will continue as usual – Click here to find out more

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: www.sicklecellsociety.org/coronavirus-and-scd/

Rise Up for Sickle Cell

Reverse Psychology London is partnering with the Sickle Cell Society to host ‘Rise Up For Sickle Cell’ a glamorous evening of celebration and fundraising on Thursday 22nd July 2021.

Join us for an evening of music, art, fashion, food and more at the exclusive Home House private members club. Find out more here: www.sicklecellsociety.org/riseup/

Give Blood, Spread Love, England

Give Blood, Spread Love, England is the Sickle Cell Society’s blood donation project. We work with black-heritage communities to: raise awareness of the need for ethnically matched blood to treat people with sickle cell; increase levels of confidence in giving blood and recruit new donors to the blood donation register. Click here to find out more

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 here to find out more

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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