Sickle Cell Anemia Research Paper
Sickle cell anemia (SCA) is a genetic disorder that is hereditary. It affects the blood, and is caused when the hemoglobin in blood cells are deprived in oxygen from the proteins. These cause normal round blood cells, to have are rigid sickle shape. People affected by SCA have a higher risk of death, stroke, severe attacks, and severe rushes of pain. James Herrick discovered an anemia, and found bizarre sickle-shaped cells in 1910. A treatment for the disease was discovered in the 1920s by E. Vernon Hahn and Elizabeth Gillespie, called deoxygenation. Where a chemical reaction involving oxygen atoms from a molecule are removed. Oxygen saturation testing provides information about how much oxygen the blood is carrying. They also discovered that sickle cell anemia is most common in Africans Americans.
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They have to pursue a lifestyle of healthy eating, sleeping, and exercise. To prevent and control complications of fever, stroke, problems breathing, splenic enlargement, vision loss, and severe anemia. According to NHLBI, NIH “Get Ongoing Care: Make and keep regular appointments with your SCD doctor or medical team. These visits will help to reduce the number of acute problems that need immediate care. Coping With Pain: Work with your doctor to develop a pain management plan that works for you. This often includes over-the-counter medicines, as well as stronger medicines that you get with a prescription. A heating pad, a warm bath, a massage, physical therapy, acupuncture can be used. Distracting and relaxing activities, such as listening to music, talking on the phone, or watching TV. When families and friends give love and support to people with SCD, they can help to relieve stress and sadness. Let your loved ones know how you feel and what you need.” Furthermore, this explains how sickle cell anemia changes the lives of individuals and their
They have to pursue a lifestyle of healthy eating, sleeping, and exercise. To prevent and control complications of fever, stroke, problems breathing, splenic enlargement, vision loss, and severe anemia. According to NHLBI, NIH “Get Ongoing Care: Make and keep regular appointments with your SCD doctor or medical team. These visits will help to reduce the number of acute problems that need immediate care. Coping With Pain: Work with your doctor to develop a pain management plan that works for you. This often includes over-the-counter medicines, as well as stronger medicines that you get with a prescription. A heating pad, a warm bath, a massage, physical therapy, acupuncture can be used. Distracting and relaxing activities, such as listening to music, talking on the phone, or watching TV. When families and friends give love and support to people with SCD, they can help to relieve stress and sadness. Let your loved ones know how you feel and what you need.” Furthermore, this explains how sickle cell anemia changes the lives of individuals and their