Sickle cell disease

an advanced clinical practitioner pointing at an ultrasound image of someone's veins on a screen

On this page you can find out information about the range of services we provide at the Trust for people living with sickle cell disorder and advice for people living with the condition.

Sickle cell disease is a genetically inherited blood disorder. People with the condition disease produce sickle-shaped red blood cells that can block blood vessels and restrict oxygen supply. This can trigger a sickle cell crisis that causes severe pain and may require hospital admission.

  • Infections
  • Chest crisis
  • Stroke
  • Gall stones
  • Eye changes
  • Hip and shoulder joint problems
  • Kidney impairment
  • Leg ulcers
  • Pregnancy complications
  • Priapism (painful erection)

Many of these are preventable or have effective treatments and your health can be maintained with regular medical follow-ups.

Acute Sickle Cell Unit (ASCU)

An Emergency Department bypass unit for adults over 18 years who are experiencing a sickle cell crisis.


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Sickle cell and thalassaemia psychology (adults)

Psychological support for adults and young people age 16 and over who are living with sickle cell disorder or thalassemia.

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Sickle cell and thalassaemia psychology (children and young people)

Psychological support for children and young people living under 16 who are living with sickle cell disorder or thalassemia.

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Living with sickle cell disease

Advice about managing your health and wellbeing.

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