The Sickle Cell Society believes that every sickle cell sufferer has 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.
Over the past 30 years our society has donated nearly £2 million pounds to research, and has published documents, like the National Standards for Clinical Care in Thalassaemia.
National Society of Genetic Counsellors
National Society of Genetic Counsellors
GeneClinics
Nature (Science Journal)
The Lancet (Science Journal)
Science Magazine
New Scientist
Scientific America
Information for patients as provided by GPs during consultations.
Wolverhampton City Council home page.
Wolverhampton Primary Care Trust
This website is designed to tell you about our work and the services the PCT provide to improve health and well-being in the city of Wolverhampton.
NHS Sickle Cell & Thalassaemia Screening Programme
This website contains information about sickle cell and thalassaemia and other haemoglobin disorders, about the tests offered at different stages of life, and about how screening and care are being developed.
