Sickle Cell Society

Sickle Cell Society company information, Employees & Contact Information

The Sickle Cell Society believes that individuals with sickle cell disease 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. Both sexes are equally affected, and should have equal access to support and services within a confidential and sensitive environment. We respect the views of every patient. We have a network of committed volunteers, who play an important part in running the charity, providing administrative backup, and helping with fund-raising activities. Donations from the public, fund-raising activities and membership fees are also part of our life support. Without them, we would be unable to finance the essential welfare, research and educational projects and we would be unable to offer children a much-needed holiday. The Society benefits from the support of a wide range of individuals and organisations nationally, who together play a vital role in its success. It draws funding support from amongst others the Department of Health, Community Fund, Lloyds TSB Foundation, PPP Healthcare Medical Trust and Goldman Sachs International.

Company Details

Employees
36
Founded
-
Address
54 Station Road, London,london Nw10 4ua,united Kingdom
Phone
+44 0 20 8961 7795
Email
in****@****ety.org
Industry
Hospitals And Health Care
NAICS
Health Care and Social Assistance
Social Assistance
HQ
London, London
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Sickle Cell Society Questions

News

Are patients with sickle cell disease still being failed by the healthcare system? - The BMJ

Are patients with sickle cell disease still being failed by the healthcare system? The BMJ

'Sickle cell isn't just on Supacell': Konnor Ewudzi and his family open up about their experience on World Sickle Cell Day - The Scotsman

'Sickle cell isn't just on Supacell': Konnor Ewudzi and his family open up about their experience on World Sickle Cell Day The Scotsman

Love Island star opens up on tragedy that saw cousin die ‘out of the blue’ - The Sun

Love Island star opens up on tragedy that saw cousin die ‘out of the blue’ The Sun

Recognising the competencies for sickle cell and thalassaemia counselling - Nursing Times

Recognising the competencies for sickle cell and thalassaemia counselling Nursing Times

World Sickle Cell Day Celebrates Patients, Raises Awareness - Sickle Cell Disease News

World Sickle Cell Day Celebrates Patients, Raises Awareness Sickle Cell Disease News

Establishing a Sickle Cell Disease Registry in Africa: Experience From the Sickle Pan-African Research Consortium, Kumasi-Ghana - Frontiers

Establishing a Sickle Cell Disease Registry in Africa: Experience From the Sickle Pan-African Research Consortium, Kumasi-Ghana Frontiers

Remembering Windrush: Honouring the Legacy and Advocating for Sickle Cell Disorder - Imperial College Healthcare NHS Trust

Remembering Windrush: Honouring the Legacy and Advocating for Sickle Cell Disorder Imperial College Healthcare NHS Trust

Spotting the signs of sickle cell disease and how to respond - RCNi

Spotting the signs of sickle cell disease and how to respond RCNi

Campus goes red to support sickle cell awareness - Campus Echo Online

Campus goes red to support sickle cell awareness Campus Echo Online

Sickle Cell Society Report – Shortage of Specialised Sickle Cell Nurses - Manchester University NHS Foundation Trust

Sickle Cell Society Report – Shortage of Specialised Sickle Cell Nurses Manchester University NHS Foundation Trust

'Poetry helped me grieve my sister - now I use it to give £5000 to families at Christmas' - The Mirror

'Poetry helped me grieve my sister - now I use it to give £5000 to families at Christmas' The Mirror

Supacell cast tackle Sickle Cell at Theatre Peckham - voice-online.co.uk

Supacell cast tackle Sickle Cell at Theatre Peckham voice-online.co.uk

Sickle cell symptoms as Kyra, 25, has been in hospital more than 150 times with 'pain attacks' - Wales Online

Sickle cell symptoms as Kyra, 25, has been in hospital more than 150 times with 'pain attacks' Wales Online

Leicester’s Lord Mayor sets out to raise awareness of Sickle Cell disorder - Leicester City Council

Leicester’s Lord Mayor sets out to raise awareness of Sickle Cell disorder Leicester City Council

Jourdan Dunn: ‘I thought about giving up’ - The Times

Jourdan Dunn: ‘I thought about giving up’ The Times

How schools can support pupils with sickle cell disease - Tes

How schools can support pupils with sickle cell disease Tes

Dame Elizabeth Anionwu shares adorable graduation photo - This is Money

Dame Elizabeth Anionwu shares adorable graduation photo This is Money

Sickle Cell Children & Young Person’s Peer Mentoring Programme for Manchester, Liverpool and Sheffield (North West Region) - Manchester University NHS Foundation Trust

Sickle Cell Children & Young Person’s Peer Mentoring Programme for Manchester, Liverpool and Sheffield (North West Region) Manchester University NHS Foundation Trust

The Black patient experience is still negative - voice-online.co.uk

The Black patient experience is still negative voice-online.co.uk

Dave Hill talks to parents who have passed a debilitating illness to their children - The Guardian

Dave Hill talks to parents who have passed a debilitating illness to their children The Guardian

Event highlights 'avoidable deaths' after landmark report - Liverpool Echo

Event highlights 'avoidable deaths' after landmark report Liverpool Echo

Miles, 13, has to wait and hope for bone marrow gift - Bedford Today

Miles, 13, has to wait and hope for bone marrow gift Bedford Today

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