SICKLE CELL ANAEMIA

Sickle cell anaemia (SCA) is an inherited red blood cell (RBC) disorder. RBCs contain a protein called 'haemoglobin' which binds to oxygen and transports it from the lungs to tissues and organs around the body. People who suffer from SCA produce abnormal haemoglobin, impairing the blood's ability to carry oxygen to the tissues and organs around the body. Abnormal RBCs are produced in people living with SCA, which are shaped like sickles or crescent moons, as shown in the image below. These sickle cells are sticky and rigid, meaning they can get stuck in blood vessels, blocking blood flow and oxygen delivery.

 
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As SCA is an inherited, recessive condition, people must receive one sickle cell gene from their mother and one from their father to be diagnosed with SCA. SCA is more common in people with an African or Caribbean family background, and approximately 12,500-15,000 people are living with SCA in the UK, making it the most common inherited blood disorder.

People living with SCA suffer from extremely painful episodes known as 'sickle cell crises'. This happens when sickle cells get stuck in blood vessels blocking blood flow throughout the body. People with SCA may be given blood transfusions to increase the number of normal, healthy RBCs in their blood, and as they can experience severe symptoms and infections, they may need blood transfusions once or twice a month to manage their symptoms and improve oxygen delivery throughout the body.

The NHS needs donors from all ethnic backgrounds to meet the needs of all patients. When someone receives a blood transfusion, they need blood from someone who is closely matched to their own blood type. The best blood type match typically comes from those with the same ethnic background, and as SCA is more common in people from black, Asian and minority ethnic backgrounds, the NHS needs more black and Asian donors to donate and help people who suffer from blood disorders such as SCA.

  • TITO'S STORY

    To learn more about what it’s like to live with sickle cell anaemia, read Tito’s story: