June 19 Is World Sickle Cell Day: Get the Facts
How much do you really know about this blood disorder?
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The 411 on Sickle Cell - June 19 is World Sickle Cell Day. Sickle cell disease (SCD) is a serious genetic disease that is especially prevalent among African-Americans. Yet, how much do you really know about this inherited blood disorder? —Kellee Terrell(Photo: Courtesy African American Blood Drive and Bone Marrow Registry for Sickle Cell Disease Awareness)
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What Is Sickle Cell Disease? - SCD is an inherited disease in which the red blood cells in your body are shaped in sickles with jagged edges as opposed to smooth ovals or discs. People with SCD have red blood cells that contain mostly hemoglobin S, an abnormal type of hemoglobin. The most common form of SCD is sickle cell anemia. (Photo: Getty Images)
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What Are the Complications? - SCD can have some devastating symptoms including pain, swelling, numbness, tingling or redness of the hands or feet. It can also cause infections, lung issues, bone deterioration, asthma, hypertension, gallstones, stroke and even death. The symptoms can be mild for some and severe for others.(Photo: Blend Images/Getty Images)
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How Do You Treat It? - Depending on the severity of the illness, treatment can be a combination of antibiotics, pain management, intravenous fluids, blood transfusion and surgery. Droxia — a cancer drug — has been approved to treat sickle cell in adults. It helps reduce severe pain, acute chest syndrome and the need for blood transfusions in adult patients. (Photo: Joe Raedle/Getty Images)
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Iron Overload and SCD - While blood transfusions are a common form of treatment that can help people with SCD, this extra blood introduces more iron in the body. This is especially the case for those who have had 10 or more transfusions. Excess iron just does not go away on its own and can linger in the body. It can build up causing damage to the heart, liver and other organs. (photo: GettyImages)
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