What is Sickle Cell?

The most common and fastest growing genetic condition in the UK.

Sickle Cell is the name for a group of different but similar inherited health conditions that affect haemoglobin. It gets its name because the red blood cells — which are normally round and flexible — become shaped like a crescent moon or farmer's sickle.

The unusually-shaped red blood cells are rigid and can block blood vessels, reducing blood flow to parts of the body resulting in excruciating pain known as a Sickle Cell crisis. This can sometimes cause damage.

Red blood cells

Sickle Cell Symptoms

Sickle Cell Crisis (excruciating pain episodes when sickled cells block blood vessels)
Stroke (common between the ages of 2 and 16)
Blindness
Organ failure
Pulmonary hypertension
Acute chest syndrome
Leg ulcers
Gallstones
Headaches and severe fatigue

Did You Know?

1 in 7

Adults of African and Caribbean descent in the UK carry the Sickle Cell gene

15,000+

People in the UK have Sickle Cell

250,000+

People in the UK have Sickle Cell trait

Things That Can Cause Sickling

Dehydration

Infection

Excessive exercise

Organ failure

Stress and anxiety

Sudden change in temperature

Treatments for Sickle Cell

Blood transfusions and red cell exchange

May be necessary to prevent strokes, improve oxygen delivery during acute chest syndrome, and prevent complications before operations.

Hydroxyurea

A drug shown to improve symptoms by reducing pain episodes and the need for blood transfusions in Sickle Cell.

Bone marrow transplant

Currently the only cure for Sickle Cell. While many survive, 1 in 10 will not. Finding a match can be difficult.

Gene therapy

The future cure to replace the defective gene with a normal gene.

Folic acid

Helps the body make new red blood cells. The anaemia in Sickle Cell is caused by haemoglobin S where red blood cells don't live as long.

Penicillin

Children with Sickle Cell are 600 times more likely to get pneumococcal infection because their spleen doesn't filter infection properly.

Healthy diet and hydration

Hydration is critical — insufficient water can trigger a crisis. A balanced diet supports red blood cell production.

L-glutamine oral powder (Endari)

Works by increasing glutamine in the blood, taken up by sickle cells to release antioxidants that lessen pain and swelling. Approved in the USA, awaiting NICE approval in the UK.

Sickle Cell FAQs