P.O. Box 4186
Little Rock, AR 72214
ph: 501-650-0764
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What is sickle cell anemia disease?
Sickle cell anemia disease is an inherited disease of red blood cells. Individuals with sickle cell disease have abnormal hemoglobin, the protein inside red blood cells that carries oxygen to every part of the body. The abnormal hemoglobin causes the red blood cells to become C-shaped (like a farm tool called a sickle) and stiff.
Normally, red blood cells are round and flexible and flow easily through blood vessels. Stiff red blood cells get stuck in tiny blood vessels, cutting off the blood supply and causing pain and, sometimes, organ damage. Sickle-shaped red blood cells die and break down more quickly than normal red blood cells, resulting in anemia.
There are several common forms of sickle cell disease:
Sickle cell trait (also known as being a carrier) occurs when a person has one gene for sickle hemoglobin and one gene for normal hemoglobin. Approximately one in ten African-Americans carries sickle cell trait. People who are carriers generally do not have any medical problems and lead normal lives. If you are a carrier you cannot develop sickle cell disease.
Find the informational brochures below on sickle cell disease. Please click on the link below. These materials are compliments of the CDC and NIH.
Tool Kit for Living Well With Sickle Cell
Fact Sheet: Sickle Cell Disease and College
Fact Sheet: Sickle Cell and Pregnancy
Fact Sheet: Sickle Cell Trait
Living Well With Sickle Cell Disease
Five Tips to Prevent Infection
What is hemoglobin?
Hemoglobin is found in all red blood cells and carries oxygen from the lungs to tissues and organs throughout the body. Normal red blood cells are soft, smooth, round and can move easily through the body. When affected by sickle cell disease, the red blood cells become rigid, sticky, and sickle shaped. This results in periodic plugging of blood vessels, thereby preventing delivery of oxygen to tissues and organs.
P.O. Box 4186
Little Rock, AR 72214
ph: 501-650-0764
contactu