A nurse is caring for a patient with sickle cell anemia exhibiting signs of vaso-occlusive crisis.
A series of blood abnormalities known as sickle cell disease (SCD) are frequently inherited from one's parents. The most typical variety is referred to as sickle cell anemia. The oxygen-carrying protein hemoglobin found in red blood cells becomes aberrant as a result. In certain cases, this results in a hard, sickle-like form. Sickle cell disease problems often start at the age of 5 to 6 months. Anemia, swelling in the hands and feet, bacterial infections, stroke, and pain episodes (also known as sickle cell crises) are just a few of the health issues that could arise. As people age, they may experience chronic pain. In the developed world, people typically live between 40 and 60 years.
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