Sickle Cell disease, also known as SCD, is a genetic disease of a person’s red blood cells. The shape of a normal person’s red blood cells also known as RBC is shaped like a disk. This shape of the red blood cells allows for the flexibility that helps the cells move through blood vessels. However, in a Sickle Cell patient’s case, the shape of the red blood cell is similar to a crescent. Research says that the name of this blood disorder was actually named after a tool called a Sickle hence the name Sickle Cell.
Sickle Cell is said to have originated in four places within Africa and the Indian/Saudi Arabian subcontinent. However there are reports “Walter Clement Noel who is said to be the first person described with Sickle Cell Disease” (Steensma). This disease was first described by an internist by the name of James Bryan Herrick. Today an estimated 70,000 out of 100,000 Americans have or is effected by Sickle Cell disease.
Sickle Cell Disease is so uncommon that people have failed to realize that there is more than one type of Sickle Cell Disease. In fact, there is a vast number of different Sickle Cell disease. The most recognized types of Sickle Cell Disease are Hemoglobin SS Disease, Hemoglobin SC Disease, ...
... middle of paper ...
...s no abnormality in the brain. Pulse oximetry is usually tested at medical sites to check the level of oxygen in a person’s blood. The next test that is usually performed is the Ultrasound. Although the ultrasound is often known for being given to pregnant women this test is also given to SCD patients to observe different organs that may be at risk. The last test is the Echocardiogram (ECG).this test is given to check the heart which is very important with SCD patients who may have heart deficiencies.
Although Sickle Cell is not a very well-known disease, thousands of people are being diagnosed and are living with this disease. Hopefully there will soon be a silver lining in the sky and hope for a better tomorrow for those who are affected by SCD. Patients all around the world will hopefully live a more relaxed life knowing that they are not being “ignored” anymore.
Need Writing Help?
Get feedback on grammar, clarity, concision and logic instantly.Check your paper »
- While people are trying to find a breakthrough cure for diseases such as Cancer, Sickle Cell patients feel that they are left in the dark of the public’s eye. Each day thousands of people are being faced with the shocking truth of having to live a very hard, tiresome, and very painful life. According to researchers about one in four hundred African American is affected with Sickle Cell (“Language of Cells”). Therefore it is felt that there should be a greater effort in trying to find a cure for this life changing disease.... [tags: Red blood cell, Blood, Sickle-cell disease]
1450 words (4.1 pages)
- 1. Sickle Cell Disease is life-threatening and has a risk of of causing depression. In this study I examine the experiences that Sickle Cell patients go through specifically at emergency healthcare facilities to find out if there are any negative stigmatizations surrounding this disease. There may be judgments that are made about these patients from healthcare professionals when they seek drugs for their pain relief that may cause the stigmatization to occur. I will also investigate why individuals that have Sickle Cell Disease experience longer waiting times at emergency healthcare facilities and the lack of control they may have over their care regime.... [tags: Health care, Health care provider]
878 words (2.5 pages)
- Sickle Cell Disease is a genetic disorder that can’t be treated unless the individual has been clinically diagnosed via screening tests. Initial screening results, such as high systolic blood pressure, sex, low hemoglobin levels and oxygen saturation, can be done to give baseline results that could be used to diagnose the patients (DeBaun4). Similarly, the most common screening test is done by the collection of urine or blood being drawn and tested from a healthcare provider (NIH9). The blood test will determine if the individual being tested already has SCD or SCT.... [tags: Red blood cell, Blood, Bone marrow]
1041 words (3 pages)
- Sickle cell anemia is an inherited pathosis that must have two copies of an aberrant gene present in order for the condition to cultivate and then, transcribe the inadequate hemoglobin molecule (Ricci, Kyle, & Carman, 2013). The population that ubiquitously inherits the condition is African Americans, Southeast Asians, and Middle Eastern societies (Ricci et al., 2013). “In the United States, approximately 70,000 to 100,000 people have the disease, and 2 million have the sickle cell trait” (Ricci et al., 2013, p.... [tags: Sickle-cell disease, Red blood cell, Sickle]
950 words (2.7 pages)
- Each person has their very own genetic blueprint that makes each person a little bit different from each other. When being formed, you get half of your chromosomes from one parent and the other half from the other parent. These traits that are passed down carry any disease and other problems that may run in the family. One disease that is inherited just like your hair color or eye color would sickle cell anemia, where there are not a sufficient amount of healthy red blood cells. Sickle cell anemia is a condition where there is not an adequate quantity of red blood cells to carry oxygen throughout the body.... [tags: Red blood cell, Sickle-cell disease, Hemoglobin]
1004 words (2.9 pages)
- HEMOPHILIA AND SICKLE CELL ANEMIA Research Paper 2 Abstract Genetically passing down of blood diseases has been happening for decades. There are many diseases of the blood that have been passed down from older generations. The most medically expensive and at times fatal one is Hemophilia and Sickle Cell Anemia. If left without treatment, they can be lethal and deadly. Sometimes even treatment doesn’t make the situation much better. Sickle cell anemia is the distortion of the red blood cell shape and certain properties.... [tags: Blood, Red blood cell, Sickle-cell disease]
2115 words (6 pages)
- Sickle Cell Disease (SCD) (also known as Sickle Cell Disorder or Sickle Cell Anemia) is an inherited blood disorder where the red blood cells have abnormal sickle-shaped hemoglobin S (HbS) called sickle haemoglobin (National Heart Lungs and Blood Institute (NHLBI), 2015). The disease, according to medical sciences, is inherited from both parents as part of their genetic makeup and is usually caused by some abnormalities in haemoglobin which is a protein in red blood cells that conveys oxygen through the body.... [tags: Sickle-cell disease, Red blood cell, Malaria]
1013 words (2.9 pages)
- History of sickle cell Many people can prove to the fact that sickle cell originated in Africa. Going by different names related to tribal languages but in 1910 a young dental student came to the office of Doctor James B. Herrick, a cardiologists complaining of black problems Herrick wanted nothing to do with young kids. So he referred him to Dr.Ernest Irons after drawing flood and examines it. Dr.Irons notice that the red blood cells had a sickle shape at that moment he immediately informed Dr.... [tags: Red blood cell, Sickle-cell disease, Hemoglobin]
1615 words (4.6 pages)
- Interventions for Children with Sickle Cell Disease Children with Sickle Cell Disease According to the Centers for Disease Control and Prevention (CDC), sickle cell disease (SCD) affects millions of people worldwide and predominantly affects descendants from sub-Saharan Africa, South and Central America, the Caribbean, Saudi Arabia, India; and the Mediterranean. Sickle cell disease is a genetic disorder of the red blood cells where the red blood cells comprises of predominantly hemoglobin S, an abnormal type of hemoglobin (2011).... [tags: interventions, center for disease control]
2200 words (6.3 pages)
- Background It is estimated that there are 100,000 people living with sickle cell disease (SCD) in the United States.1 Clinically, SCD can lead to acute and chronic symptoms that include not only pain syndromes, but also hemolytic anemia and its derivatives. The most common characteristic of SCD is vaso-occlusive pain crises (VOCs), which are characterized by irregular, unanticipated episodes of severe pain caused by occluded blood vessels. Furthermore, these crises could occur at any time during the year or during several years, leading to urgent, unexpected situations.... [tags: Pain, Patient, Sickle-cell disease, Hospital]
1621 words (4.6 pages)