Symptoms of sickle cell disease

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Sickle cell disease symptoms can be different for each person, but the most common symptoms are anemia and pain. Read about why these symptoms happen in people with sickle cell disease.

Key points

  • How often a person experiences symptoms of sickle cell disease, and how severe the symptoms are, can vary from time to time and from person to person.
  • The most common symptoms of sickle cell disease are anemia and pain.
  • Pain and anemia occur when sickle cells get stuck in blood vessels and cannot deliver enough oxygen around the body.

The frequency and severity of symptoms of sickle cell disease can vary from time to time and can be different for each person. They can range from mild to severe.

The most common symptoms are anemia and pain.

Anemia

Most people with sickle cell disease have anemia. This is a condition where the blood cannot deliver enough oxygen around the body.

In someone with sickle cell disease, anemia occurs because their red blood cells:

  • do not contain normal hemoglobin.
  • do not last as long as regular blood cells. A normal red blood cell lives about three to four months, but a sickle cell usually survives for less than 20 days.

If your body cannot get enough oxygen for its needs, you may have fatigue, shortness of breath and poor concentration.

Pain

Pain can have many different causes. In people with sickle cell disease, the most common cause is the sickling (“curving”) of red blood cells.

When sickle cells can’t flow freely in a blood vessel, they become stuck. As a result, the area of the body supplied by that blood vessel does not get enough oxygen. The lack of oxygen can cause the affected part of the body to feel pain and become inflamed.

Sickle cell pain can happen anywhere in the body, but it is most common in the arms, legs, chest, back and abdomen.

For more information on pain, see What is pain?


Dernières mises à jour: septembre 25th 2023