Symptoms of sickle cell disease
People born with sickle cell disease tend to have problems from early childhood, although some children have few symptoms and lead normal lives most of the time.
The main symptoms of sickle cell disease are:
- painful episodes called sickle cell crises, which can be very severe and last up to a week
- an increased risk of serious infections
- anaemia (where red blood cells cannot carry enough oxygen around the body), which can cause tiredness and shortness of breath
Some people also experience other problems, such as delayed growth, strokes and lung problems.
Causes of sickle cell disease
Sickle cell disease is caused by a gene that affects how red blood cells develop.
If both parents have the gene, there's a 1 in 4 chance of each child they have being born with sickle cell disease.
The child's parents often will not have sickle cell disease themselves and they're only carriers of the sickle cell trait.
Screening and testing for sickle cell disease
Sickle cell disease is often detected during pregnancy or soon after birth.
Screening for sickle cell disease in pregnancy is offered to all pregnant women in England to check if there's a risk of a child being born with the condition, and all babies are offered screening as part of the newborn blood spot test (heel prick test).
Blood tests can also be carried out at any age to check for sickle cell disease or see if you're a carrier of the gene that causes it.
Treatments for sickle cell disease
People with sickle cell disease need treatment throughout their lives. This is usually delivered by different health professionals in a specialist sickle cell centre.
It's also important for people with sickle cell disease to look after their own health using self care measures, such as by avoiding triggers and managing pain.
A number of treatments for sickle cell disease are available.
- drinking plenty of fluids and staying warm to prevent painful episodes
- painkillers, such as paracetamol or ibuprofen (sometimes treatment with stronger painkillers in hospital may be necessary)
- daily antibiotics and having regular vaccinations to reduce your chances of getting an infection
- a medicine called hydroxycarbamide (hydroxyurea) to reduce symptoms
- regular blood transfusions if symptoms continue or get worse, or there are signs of damage caused by sickle cell disease
- an emergency blood transfusion if severe anaemia develops
The only cure for sickle cell disease is a stem cell or bone marrow transplant, but they're not done very often because of the risks involved.
Outlook for sickle cell disease
Sickle cell disease varies between individuals from mild to serious, but most people with it lead happy and normal lives.
Mild sickle cell disease may have no impact on a person's day-to-day life.
But the illness can be serious enough to have a significant effect on a person's life.
It can lead to health problems like strokes, serious infections and lung problems, which can occasionally be fatal.
Overall, the life expectancy for someone with sickle cell disease tends to be shorter than normal, but this can vary depending on the exact type of sickle cell disease they have, how it's treated and what problems they experience.
Carriers of sickle cell (sickle cell trait)
A carrier of sickle cell is someone who carries the gene that causes sickle cell disease but does not have sickle cell disease themselves. It's also known as having the sickle cell trait.
People with the sickle cell trait will not develop sickle cell disease, but are at risk of having a child with it if their partner is also a carrier.
You can request a blood test to check if you carry the sickle cell trait from your GP surgery or the nearest sickle cell and thalassaemia centre.
The sickle cell support group
Finding out as much as possible about sickle cell disease may help you feel more in control of your illness.
The Sickle Cell Society is a UK charity for people with sickle cell disease.
Their website has a wide range of useful information, including news about research into the disorder.