Paid Vacancy : Family Retreat Coordinator
We are looking to recruit an energetic, proactive and relentlessly organised person to coordinate, manage... Read More
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Get In Touch
The best way to get in touch is to complete our short Contact Form which will direct your enquiry to the right member of staff: www.sicklecellsociety.org/contact/
We also have a FAQ page where we answer commonly asked questions: www.sicklecellsociety.org/faqs/
To get in touch via phone, please see our list of project and staff phone numbers here: www.sicklecellsociety.org/contact-details/
No One’s Listening
MPs call for urgent changes to sickle cell care after inquiry finds “serious failings”
An All-Party Parliamentary Group (APPG) inquiry report published today highlights shocking failures as cross-party MPs call for major changes into care for sickle cell patients.
Find out more and read the full report here: www.sicklecellsociety.org/no-ones-listening/
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/
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.
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…
Latest News
Tender Opportunity: External Audit Services for Sickle Cell Society
We’re inviting tenders from suitably qualified and competent registered auditors with a high level of knowledge... Read More
Exploring New Treatment Options for Severe Sickle Cell Disorder : The Redress Study
Exploring New Treatment Options for Severe Sickle Cell Disorder: The REDRESS study Living with... Read More
