Sickle cell anemia is a condition of the blood. The condition is genetic and is when the red blood cells are mutated into a crescent shape. The cells are hard and sticky which makes them easier to clot. Such aspects often mean that blood flow is cut off or slowed down from various organs in the body. Because of the nature of the disease, there are many people looking for ways of preventing sickle cell anemia. However, because this disease is heredity, there is no way of preventing it. That being said, there are methods of controlling is progress and the symptoms that go along with it.
There are different types of anemia. Sickle cell is one of these types and is considered to be a quite severe form of it. In this illness, red blood cells are mutated so that they take the shape of crescents instead of circular. This affects the flow of the blood.
These mutated blood cells are hard and sticky. They may clump together and prevent normal blood flow. Organs in the body require regular blood flow to maintain proper function. Without this, they can be damaged over time and cause numerous sorts of symptoms.
Yet another aspect of these cells that is influenced. The sickle cell only has a lifespan of between 10 and 20 days. This number is only a small percentage of the average 120 days for the normal red blood cell. The bone marrow that creates these components cannot produce them fast enough to keep up with the death rate. Therefore, the body is always short of these elements.
There are numerous signs and symptoms of this disease. The most common ones include dizziness, a shortness of breath, coldness in the feet and hands, pale skin, and jaundice. Sudden pains in various parts of the body are also common because of blocked blood flow to different organs. Complications that may be induced by the condition include infections, splenic crisis and hand-food syndrome, stroke, organ failure, and more.
There is no cure that is widely used for this condition and there is no way to prevent it. The good news is that there are remedies to help decrease the symptoms that are experienced. Treatments are available to help prevent the complication as well as to reduce the symptoms. The treatments are chosen on an individual basis according to the most severe or serious complications.
Various countries are running clinical trials and research to create better remedies. Researchers, doctors and scientists are virtually constantly looking for ways to make the quality of the lives for patients better. Aside from treatments, counseling is often offered to patients and families to help them cope.
There are numerous illnesses that are inherited. Sickle cell anemia is a blood condition that falls into this category. While there is no way to prevent the disease, there are treatments to help a person control the symptoms and reduce the risk of complications. The signs and symptoms of this illness often include pale skin, jaundice, dizziness, cold feet, cold hands, and shortness of breath. The complications are many and include stroke, organ failure, and others. While treatments can help so might therapy. Individuals may find that talking to a professional may assist them and their families in coping with their condition.
There are different types of anemia. Sickle cell is one of these types and is considered to be a quite severe form of it. In this illness, red blood cells are mutated so that they take the shape of crescents instead of circular. This affects the flow of the blood.
These mutated blood cells are hard and sticky. They may clump together and prevent normal blood flow. Organs in the body require regular blood flow to maintain proper function. Without this, they can be damaged over time and cause numerous sorts of symptoms.
Yet another aspect of these cells that is influenced. The sickle cell only has a lifespan of between 10 and 20 days. This number is only a small percentage of the average 120 days for the normal red blood cell. The bone marrow that creates these components cannot produce them fast enough to keep up with the death rate. Therefore, the body is always short of these elements.
There are numerous signs and symptoms of this disease. The most common ones include dizziness, a shortness of breath, coldness in the feet and hands, pale skin, and jaundice. Sudden pains in various parts of the body are also common because of blocked blood flow to different organs. Complications that may be induced by the condition include infections, splenic crisis and hand-food syndrome, stroke, organ failure, and more.
There is no cure that is widely used for this condition and there is no way to prevent it. The good news is that there are remedies to help decrease the symptoms that are experienced. Treatments are available to help prevent the complication as well as to reduce the symptoms. The treatments are chosen on an individual basis according to the most severe or serious complications.
Various countries are running clinical trials and research to create better remedies. Researchers, doctors and scientists are virtually constantly looking for ways to make the quality of the lives for patients better. Aside from treatments, counseling is often offered to patients and families to help them cope.
There are numerous illnesses that are inherited. Sickle cell anemia is a blood condition that falls into this category. While there is no way to prevent the disease, there are treatments to help a person control the symptoms and reduce the risk of complications. The signs and symptoms of this illness often include pale skin, jaundice, dizziness, cold feet, cold hands, and shortness of breath. The complications are many and include stroke, organ failure, and others. While treatments can help so might therapy. Individuals may find that talking to a professional may assist them and their families in coping with their condition.
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