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Sickle Cell Anemia

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Sickle cell disease prevents one of the body 's most fundamental re-sources, the blood, from adequately transporting oxygen to the tissue, which can result in organ damage and many other related complications. A sickle cell related "crisis" can be extremely painful for patients, and deadly in some cases. Both quality of life and life expectancy are reduced for sickle cell patients, even when the disease is optimally managed with existing therapies, blood transfusions, vitamin regimens and a host of other precautions. "An ISU student died March 12 from complications of Sickle Cell Anemia there is no cure for Sickle Cell Anemia" (Indiana Statesman 2004). Sickle cell disease is a group of disorders that affects hemoglobin. Hemoglobin is …show more content…

Sickle cell has a lot of different complications. These make the disease itself harder. All the complications and symptoms just depends on the person and how their body chooses to react. Hand-Foot Syndrome is one complication that occurs with sickle cell. Due to the sickling of the cells blood vessels may be blocked which causes the hands and/or feet to painfully swell. Swelling only occurs on the back of the hands and feet and moves into the finger and toes. This may be the first sign of sickle cell in infants. The spleen helps filter out abnormal red blood cells and helps fight infections. At times the spleen traps many cells that should be in the bloodstream and it grows large. This causes anemia. Pneumonia is the most common cause of death in young children. When the sickled cells get trapped in the lungs acute chest syndrome begins to occur. Stroke and eye problems also occur with sickle cell. When it comes to males that have sickle cell priapism can occur. That is when males have a painful and unwanted erection. This occurs because the sickle cells stop blood flow out of an erect penis. Over time, priapism can damage the penis. Some other complications are gallstones, ulcers on the legs, high blood pressure, and multiple organ failure. Having sickle cell is not all fun and

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When the patient is sent home, the goal is to prevent readmission to the hospital due to complications of SCD. Sammy’s poor decisions leading up to this ER admission and past medical history should be discussed in detail with the patient. The nurse should also address possible triggers of a sickle cell crisis with the patient. (Reddin et al., 2011). In Sammy’s case, discarding lunches and drinks at school significantly contributed to being dehydrated making this one of his triggers.

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One of the concluding sentences that Dr. Sharon Moalem directs toward her audience is, “[...] Our relationship with disease is often much more complex than we may have previously realized.” “Survival of the Sickest” delves into the theme of the way inheritance and genetic codes in our bloodlines allows fatal diseases to enter our body and the reasons for this happening. The author discusses various diseases and their origin, and includes facts as to how this disease is able to affect modern life. She suggests that said modern diseases played a necessary part in the survival and selection of those before us in our history.

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683 Words | 3 Pages

Symptoms of sickle cell include, chronic pain, infection, swollen hands and feet and of course Anemia along with other serious symptoms. 1. However this symptom can vary from person to person and some have no symptoms at all. B. Sadly, there is no cure for this disease. 1.

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1104 Words | 5 Pages

Sickle Cell Disease is an inherited blood disorder in which the red blood cells that carry the oxygen throughout the body are sickle-shape. The sickle-shaped cells often cause the blood to clot and lead to a pain crisis .Here is a brief history of the agency in which I volunteered at is as follows: The Sickle Cell Disease Association of America – Mobile Chapter (SCDAA-MC) is a 501(c)(3) nonprofit organization, governed by a volunteer Board of Directors. The Chapter was incorporated in 1976 and is a United Way partner agency. The Association works closely with the Alabama Department of Public Health, USA Comprehensive Sickle Cell Center, Franklin Primary Health Center, local county health departments, and the Guadalupe Center (History of the

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A group of inherited red blood disorder in which the red blood cell forms a C-shaped and becomes hard and stick together is known as sickle cell disease (SCD). These sickle cells has a short life span which causes shortage in red blood cells and sometimes clog the blood flow in the small blood vessels causing pain, infection acute chest syndrome and stroke (CDC, 2015). Patient with SCD most often has cellular sickling known as crises which began suddenly and continues frequently or seldomly. Sickle cell crisis is a response to deficient oxygen in the blood which could be local or systemic. Hypoxia, anoxia, ischemia, and cell death of tissue and organs can occur as a result of repeated larger blood vessels naso-occlussive event.

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