What is the lifespan of someone with sickle cell anemia?

Results: Among children and adults with sickle cell anemia (homozygous for sickle hemoglobin), the median age at death was 42 years for males and 48 years for females. Among those with sickle cell-hemoglobin C disease, the median age at death was 60 years for males and 68 years for females.

Can you get malaria with sickle cell?

It is believed that the current prevalence of malaria in endemic areas reflects selection for the carrier form of sickle cell trait through a survival advantage. Malaria has been incriminated as a great cause of mortality in people with sickle cell disease (SCD).

What is the survival rate of sickle cell anemia?

Data from the 1995 cooperative study of SCD (CSSCD) suggested that the median survival for individuals with SCD was 48 years for women and 42 years for men. This life expectancy was considerably lower than that for African Americans who do not have SCD.

Can a person die from sickle cell anemia?

The body cannot replace the lost cells fast enough. As a result, the body has too few red blood cells, a condition known as anemia. Sickle cell anemia is a serious disease that can require frequent hospital stays. Children and young adults can die from the disease.

How many people have died of sickle cell anemia?

About 1 in every 365 black or African American babies is born with sickle cell disease. There are also many people who have sickle cell disease who come from Hispanic, southern European, Middle Eastern, or Asian Indian backgrounds. About 100,000 Americans have sickle cell disease.

How does sickle cell anemia affect my quality of life?

Sickle cell anemia can make life more difficult, particularly for a child, who will need to deal with delayed sexual maturity and stunted growth. You will need to avoid things that can cause a crisis, such as certain medication that restricts blood vessels, high altitudes, and strenuous exercise.