Summary: The Sickle Cell Disease

Improved Essays
The Sickle Cell Disease is a very interesting but harmful disease.The Sickle Cell Disease was founded when a man named Walter Clement Noel went Dr. James B. Herrick office and asked if he had Anemia because he felt that he had the symptoms of Anemia. Anemia happens when that person doesn’t have enough red blood cells to carry oxygen to the body. Since Dr. Herrick did care about the compliments that Noel did, he sent Noel with Dr. Irons. When Dr. Irons took a look at Walter’s blood under a microscope and found out that the red blood cells were shaped like a sickle. This means it was shaped like a C. When Herrick saw this, he became more interested because he thought that he might find out a new and unknown disease.
The Sickle Cell Disease is

Related Documents

  • Improved Essays

    Chi Square Test Lab Report

    • 2147 Words
    • 9 Pages

    Sickle cell disease is an inherited disorder that is caused by a mutation in the DNA sequences that codes for the beta chain of the hemoglobin protein. Red blood cells are, normally, flexible and round, but with the sickle cell anemia the red blood cells become sticky, rigid, and crescent shaped. The Hemoglobin protein carries oxygen in the red blood cells throughout the body. With the disease, the blood cell’s shape can cause them to get lodged in the blood vessels resulting in the obstruction of blood flow, especially in the smaller arterial vessels in the body This occurrence not only reduces oxygen content to the area of concern, but can be a very painful experience for the victim. People who inherit this disease have two abnormal hemoglobin…

    • 2147 Words
    • 9 Pages
    Improved Essays
  • Improved Essays

    I am in support of the “Sickle Cell Disease Research, Surveillance, Prevention, and Treatment Act of 2015.” Sickle Cell is a serious blood disorder that causes red blood cells to become misshaped. These abnormally shaped red blood cells can get clustered into blood vessels and block blood flow to areas of the body. According to the center of disease and control the number of people with sickle cell in the united states is unknown, but it is prevalent amongst African-Americans occurring in 1 out of 365 births.…

    • 800 Words
    • 4 Pages
    Improved Essays
  • Improved Essays

    Sickle cell is a disease that affects the circulatory system. The circulatory system is in charge of moving nutrients throughout the entire body with the use of the blood stream. According to hopkinsmedicine.org the circulatory system moves nutrients, water, and oxygen to the your billions of body cells and carries away wastes like; carbon dioxide that body cells create. The circulatory system includes; the heart: which keeps the circulatory system working at all times with its constant pumping; the arteries: which carry oxygen-rich blood away from the heart to where it is needed; veins: they carry oxygen-less blood to the lungs where they have their oxygen then replenished; and lastly the blood,it is like the liquid train of the circulatory…

    • 656 Words
    • 3 Pages
    Improved Essays
  • Superior Essays

    The Gale Encyclopedia of Alternative Medicine stated that the genetic mutation associated with sickle-cell anemia occurred thousands of years ago and continued to pass down through generations. The mutation holders were less likely to be affected by malaria (Kapes, 2009). More research on the effects of sickle-cell anemia and malaria was conducted by Dr. Allison of the British Medical Journal. He found studies in Northern Rhodesia, an area greatly affected by malaria, that indicated a positive connection between sickle-cell anemia and malaria. 9.8 percent of sicklers had…

    • 1478 Words
    • 6 Pages
    Superior Essays
  • Improved Essays

    Sickle cell disease is a major health burden in the Indian community. It contributes to millions of deaths worldwide however it is most prevalent in tribal populations in the rural sectors of India. “Sickle cell disease or SCD is an inherited abnormality of the red blood cell characterized by chronic haemolytic anemia with numerous clinical consequences” (Ugwu 87). The shape of hemoglobin, which gives red blood cells their color is turned from an oval to a crescent shape when the sickle cell gene is present. The sickle shaped cells cause blockage of capillaries which leads to many symptoms such as chronic pain, pneumonia, severe anemia, and increased risk for infections (Powars 1).…

    • 1228 Words
    • 5 Pages
    Improved Essays
  • Great Essays

    Sickle Cell Anemia is a blood disorder that causes red blood cells to become misshapen and not live as long as a regular blood cell. Sickle Cell is a disease that is not very common in the world. In the United States, Sickle Cell Anemia affects between 70,000 and 100,000 people and occurring in 1 out of every 36,000 births. Sickle Cell is more likely to occur in somebody from Africa, South or Central America, the Caribbean islands, Mediterranean countries, India or Saudi Arabia. The usual age that people who have sickle cell is around 42 years for males and around 48 years for females.…

    • 749 Words
    • 3 Pages
    Great Essays
  • Improved Essays

    Identify the disease process presented by the case study as well as the normal structure and function of the organ system and/or physiological process that has the alteration. Shawn, the main character of “The Uniformed Coach” scenario has sickle cell disease (SCD) and is suffering from a sickle cell crisis. Sickle cell disease is a form of hemolytic anemia that is inherited; being caused by an abnormal hemoglobin molecule. There are several forms of SCD but the most severe is simply called sickle cell anemia; the dysfunctional hemoglobin molecule, called hemoglobin S (Hb S), assumes an unusual shape when it is subject to deoxygenation or dehydration (McCance & Huether, 2014). In a normal person, all hemoglobin molecules are shaped like…

    • 1703 Words
    • 7 Pages
    Improved Essays
  • Improved Essays

    Sickle Cell Research Paper

    • 1293 Words
    • 6 Pages

    Introduction Sickle cell disease is a genetic disorder that can be best described as irregular shaped red blood cells that block blood flow, which cause chronic periodic episodes of pain. Sickle Cells affects over 72,000 Americans and millions throughout the world, Sickle cell most commonly affect African American descent, approximately 1 in 12 African Americans carry the trait for Sickle cell and 1 of every 350 African-American infants born have the disorder and the incidence of the disorder in Africa is ten times higher (AAFP,2000). This paper will highlight background information, causes, diagnosis and discuss several treatment and therapies of Sickle cell disease and why African American are largely affected by this disease. Background…

    • 1293 Words
    • 6 Pages
    Improved Essays
  • Improved Essays

    Sickle Cell Disease (SCD) is an inherited blood disorder, in which people have abnormal hemoglobin. This causes a variety of problems for the person throughout their entire life, but severity of the disease varies. Sickle Cell Disease is not necessarily deadly, but it decreases the average life expectancy of a persson. In countries like the United states, a person with Sickle Cell Disease has a life expectancy of about forty to sixty years. Other than stem cell transplants there is no cure for Sickle Cell Disease currently, but if discovered early regular medical care and treatments can not only prolong the life of a person with the disease, it can also improve their quality of life.…

    • 903 Words
    • 4 Pages
    Improved Essays
  • Improved Essays

    Identify one intervention that can be taken by the RN to reduce the stigma and improve management of acute and chronic pain associated with Sickle Cell Disease, (SCD). One intervention that comes to my mind after reading the articles would be recognizing the cues to an acute pain episode and responding appropriately and in a timely manner (Jenerette & Ataga, 2014). By doing so, it could help manage the chronic pain associated with sickle cell disease. Patients with SCD are often stigmatized as addicted to opioids, disbelieved or mistrusted regarding reports of pain and not being allowed to participate in their own health care (Jenerette & Ataga, 2014).…

    • 279 Words
    • 2 Pages
    Improved Essays
  • Improved Essays

    Sickle cell crisis is an acute condition of sickle cell anemia. Sickle cell anemia is a genetic condition. Both parents must be carriers of the gene in order for a baby to be born with sickle cell anemia. In the United States, the gene predominantly affects black people of African decent. Sickle cell anemia is a disease where there is an inadequate number of healthy red blood cell throughout the body.…

    • 932 Words
    • 4 Pages
    Improved Essays
  • Improved Essays

    Sickle Cell Research Paper

    • 1038 Words
    • 5 Pages

    Sickle Cell Sickle cell is a blood disease that has become a more public disease amongst people. Sickle cell has been prominent since the discovery in 1910 in America. The disease was said to be around for 5000 years before that originating in East Africa. The Disease was discovered in the U.S when a patient from Granada came to Dr. Ernest Irons with anemia symptoms. The disease has a dominant gene and a recessive gene.…

    • 1038 Words
    • 5 Pages
    Improved Essays
  • Improved Essays

    He encountered multiple patients complaining of similar symptoms of acute chest pain. Dr. Herrick received a blood film, a test used to look for irregularities in red blood cells, each patient results showed signs of sickle cells. In later years’ studies showed that the disease was more common in people who are African-American, Hispanic, Central and South America descent. Currently, over 100,000 American…

    • 484 Words
    • 2 Pages
    Improved Essays
  • Improved Essays

    Sickle cell anemia is a genetic blood disorder that causes normal red blood cells to form into an irregular shape, called sickled-cells. The sickle cell gene causes the body to produce abnormal hemoglobin. After a while, the hemoglobin will then cluster together anywhere in the body causing the blockage of blood flow through the blood vessels. This blockage deprives the tissues and blood of oxygen which can lead to many difficulties and problems. SCD becomes life-threatening when the damaged red blood cells begin to breakdown, when the spleen does not work properly or at all, or when it is unable to prevent infections from coming in.…

    • 1506 Words
    • 7 Pages
    Improved Essays
  • Superior Essays

    Essay On Sickle Cell

    • 1260 Words
    • 6 Pages

    Research for Sickle Cell Disease started in 1910.When a patient from the West Indies had anemia characterized by oddly shaped red blood cells. A Chicago physician, James B. Herrick identified the red blood cells as sickled shaped. It was discovered that the sickling of the cells was associated with the low oxygen in 1927 by Hahn and Gillespie. A medical student at John Hopkins, Sherman, noticed the birefringence of deoxygenated red blood cells, recommended that low oxygen adjusted the hemoglobin structure in the molecule. In 1948 multiple individuals made discoveries.…

    • 1260 Words
    • 6 Pages
    Superior Essays