Sickle Cell Benefits

Sickle Cell Disease is an illness that affects people all across the globe. This paper will give a description of the sickness through the discussion of the causes, symptoms, and possible cures. Sickle Cell Disease (SCD) is a "group of inherited red blood cell disorders."(1) These disorders can have various afflictions, such as pain, damage and a low blood count--Sickle Cell Anemia.

“In the United States, it's estimated that sickle cell anemia affects 70,000–100,000 people, mainly African Americans” (NHLBI, NIH, Who is at risk for sickle cell anemia). SCD is a disease that is a serious disorder in which the body can make normal blood cells and sickle shape cells. Sickle shape cells can block the blood flow in your vessels and cause pain or organ damage also put you in risk for infections. SCD has no cure available but there are many treatments out there to deal with the complications of it. From over years treatments did get better from way back in the day doctors have learned. Sickle cell disease has lack of attention and funding because it’s only affecting

Sickle cell anemia can cause numerous symptoms, which the severity of this can vary between individuals. Symptoms that might vary from person to person that change over time, include anemia, episodes of pain, frequent infections, delayed growth, vision disorder, acute chest syndrome, and more. Indeed, of each symptom; anemia, sickle cell breaks red blood cell faster and die living people without enough red blood cells. Sickle cell anemia usually dies in 10 to 20 days while normal live for about 120 days before it replaced. Episodes of pain is a major symptom of this disease and the most common reason for people to get hospitalization; Pain develops when sickle-shaped red blood cells block blood flow through tiny blood vessels to the chest,

The diagnosis for the disease is straightforward. All states screen newborns for sickle cell. This can be done by a simple blood test. The treatment for sickle cell anemia is minimal. There are no cures for the disease. However treatments and pain killers can help with some of the symptoms. There are a few environmental factors of sickle cell. For example people with the disease should avoid cold areas so that their blood flow stays normal. They should also make sure that they have good circulation at all times to ensure that the blood is moving. All in all, sickle cell is a simple disease that does not take much to deal

Sickle Cell Anemia is a hereditary disease that has a gene that causes red bone marrow in the body to make sickled shapes, when this happens; it causes the red blood cells to die faster. This is what causes Hemolytic Anemia. Older children and adults with sickle cell disease may have very few complications, or have patterns of ongoing problems that ultimately shorten their lives. The most serious and common problems with sickle cell disease are organ failure, fatigue and pain. There are many opportunities and alternatives for treatment and symptom management that a sickle cell patient can consider today.

All of the cells within the tissues of the body need a regular supply of oxygen to function. The hemoglobin found in red blood cells (RBC’s) are essential for the proper transport of oxygen molecules. They bind oxygen in the lungs and carry to every tissue within the body. Due to the structure of hemoglobin, normal RBC’s are donut shaped with a concaved center. This flexible shape is what allows the BRC’s to move freely into very small spaces such as capillaries where they will deliver their oxygen. Sickle cell anemia or other diseases that fall within the broader group of disorders characterized by SCD describe conditions where the protein (hemoglobin) has misfolded and altered the shape of the cell. Sickle hemoglobin allows for the formation of stiff rods within the red blood cell giving it a sickle, or crescent shape. This new shape is not flexible and can block or slow the flow of blood. When this occurs, oxygen cannot reach its intended tissues. This results in severe pain called crises, and these attacks occur

Normal red blood cells are flexible and round and last up to four months. Sickle red blood cells are hard and sticky and looks like farm tool called a “sickle”. These cells die within twenty days which

Typically people with Sickle Cell Trait can live a normal life span; however, if anyone has this disorder severe you may contempt of dehydration and high intensity physical activity may lead to serious health issues (Sickle Cell Trait American). As research says people do not have health problems related to Sickle Cell Trait, but under stressful conditions they may have some problems. Conditions Sickle Cell Trait might also lead to low oxygen caused by stenos exercise, high altitudes which is causing a lack of oxygen (Facts about). Sickle Cell Trait is not just some disorder you can look over and never look back on it is the type you have to keep track of to keep up with how sever your case

Sickle cell disease, also known as SCD, is a hereditary blood disorder that takes place due to mutation in the hemoglobin gene that is found in red blood cells. While it is said to have originated in Africa and is mostly predominant in African Americans, sickle cell disease is now common among different ethnic groups all over the world. Sickle cell anemia (HbSS) infects “an estimated 70,000 to 100,000 Americans”(Housman) and accounts for approximately 70% of anemia in the United States. Hemoglobin functions as an oxygen carrying protein as it carries oxygen from the lungs through the arteries and to the rest of the body. In sickle cell disease,

Sickle Cell Anemia is a fatal hereditary illness with a range of signs and symptoms. A person can go years without having symptoms while some don’t survive childhood. The life span of a person with Sickle Cell Anemia is 50 years above, however female counterparts live longer than the men. It is common in African and Black individuals. The only cure for Sickle Cell Anemia is a bone marrow transplant, which reverses the illness. Hydroxycarbamide can also help lessen complications, but is not a cure. It is an illness that results in early deaths, that’s why it is important to get treatment as soon as

The condition creates when Sickle-molded red platelets hinder move through minor vessels to the midsection, mid-region, joints, and once in a while bones, bringing on great torment and distress. Torment may change in force and can keep going for a couple of hours to a couple of weeks. Some individuals encounter just a couple of scenes of torment. Others encounter twelve or more emergencies a year. In the event that an emergency is serious enough, it may oblige hospitalization. A significant muddling of Sickle cell frailty is oxygen hardship in blood and organs.

Sickle cell disease (SCD) is an inherited and noncontagious, lifelong condition. More specifically, per Ohaeri, Shokunbi, Akinlade, & Dare, 1995, SCD is a generic term for a group of genetic disorders characterized by the predominance of sickle cell hemoglobin (Hgb). Hemoglobin is a protein in the red blood cells that carries oxygen throughout the body. The disease produces significantly abnormal Hgb molecules in red blood cells (RBCs). In sickle cell anemia, the red blood cells become rigid and sticky and are shaped like sickles or crescent moons. These irregularly shaped cells can get stuck in small blood vessels, which can slow or block blood flow and oxygen to parts of the body (Ohaeri, Shokunbi, Akinlade, & Dare, 1995, p. 955.Individuals

As to this day there is really no cure for sickle cell disease. Red blood cells take oxygen from the air we breathe into our lungs to all parts of the body. Oxygen is carried in red blood cells by a substance called hemoglobin(Hemoglobin –

Normal red blood cells live in the bloodstream for about 120 days and then die, whereas sickle shaped blood cells typically last for about 10 to 20 days and the bone marrow cannot make new red blood cells fast enough to replace the dying ones (What is Sickle Cell Anaemia, 2012). Sickle cell anaemia is existent at birth, but many babies do not start showing symptoms until after 4 months of age (What are the signs and symptoms of Sickle Cell Anaemia, 2012).

Sickle Cell Anemia is a group of disorders that cause red blood cells to become misshapen and break down. Sickle cell disease is the most common inherited blood disorder in the United States, affecting 70,000 to 80,000 Americans (Ashley-Koch, Yang and Olney). Sickle Cell Anemia causes your red blood cells to be thin, stiff, and shaped like a sickle. But your red blood cells are supposed to be round and soft. A person that is diagnosed with sickle cell anemia, their blood cells start to become clogged, causing blood clots, which can cause a great amount of health issues including: infections, stroke, and acute chest syndrome. People get sickle cell anemia by inheriting a mutated gene from both of their parents. On the down side, there is not currently an effective cure for sickle cell anemia, there are several different therapeutic approaches to treating and attempting to cure the disease and help people who are affected with sickle cell anemia better manage their symptoms. There have also been several great scientists that dedicated a lot of research to help find a cure for sickle cell anemia.