Methods Of Preventing Sickle Cell Anemia
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 various sorts of anemia and sickle cell is only one of them. This being said, this particular type is also quite severe. People who are born with this condition have red blood cells in the shape of crescents instead of those shaped like circles with a hole in the center, also likened to the appearance of donuts.
Each of the sickle cells is sticky and hard. These aspects tend to cause blockages and irregularities in the blood flow. As a result, organs may be damaged over time. Patients can experience numerous symptoms and complications.
Each red blood cell that is affected also has a shorter life span than those that aren't mutated. The life span is generally between 10 and 20 days instead of 120. This means that the bone marrow has to try keep up with the depletion but it simply doesn't produce a cell fast enough.
There are various signs and symptoms displayed by patients with this illness. Individuals are often pale or have a yellowish appearance to their skin. These people often experience dizziness, cold hands, cold feet, and a shortness of breath. Patients may also feel sharp pains in their body caused by blockages in the blood vessels. Complications that may eventually form include hand-foot disease, organ failure, stroke, and splenic crisis, plus more.
Due to the nature of the illness, it can't be prevented. Individuals are born with the disease. However, treatments do exist to control the speed of progression of this illness. There are also remedies to help reduce the symptoms and well as to treat the complications. With regards to complications, it is important to have regular checkups to discover them while the treatments are still viable solutions.
Clinical trials are ongoing in various countries pertaining to the treatment of the disease. Research is constantly being done to try and make the lives of people with the condition better. Counseling is normally provided by clinics and hospitals to help patients cope.
Sickle cell anemia is an inherited disease and therefore it cannot be prevented. Such a condition is one where the patient has mutated red blood cells that are sticky and hard. These aspects often result in blocked blood flow to the organs. There are numerous symptoms and complicated that are caused by the illness. Treatments are available to slow the progress and control the symptoms. Further research is being conducted to create more remedies to improve the quality of life that patients have.
There are various sorts of anemia and sickle cell is only one of them. This being said, this particular type is also quite severe. People who are born with this condition have red blood cells in the shape of crescents instead of those shaped like circles with a hole in the center, also likened to the appearance of donuts.
Each of the sickle cells is sticky and hard. These aspects tend to cause blockages and irregularities in the blood flow. As a result, organs may be damaged over time. Patients can experience numerous symptoms and complications.
Each red blood cell that is affected also has a shorter life span than those that aren't mutated. The life span is generally between 10 and 20 days instead of 120. This means that the bone marrow has to try keep up with the depletion but it simply doesn't produce a cell fast enough.
There are various signs and symptoms displayed by patients with this illness. Individuals are often pale or have a yellowish appearance to their skin. These people often experience dizziness, cold hands, cold feet, and a shortness of breath. Patients may also feel sharp pains in their body caused by blockages in the blood vessels. Complications that may eventually form include hand-foot disease, organ failure, stroke, and splenic crisis, plus more.
Due to the nature of the illness, it can't be prevented. Individuals are born with the disease. However, treatments do exist to control the speed of progression of this illness. There are also remedies to help reduce the symptoms and well as to treat the complications. With regards to complications, it is important to have regular checkups to discover them while the treatments are still viable solutions.
Clinical trials are ongoing in various countries pertaining to the treatment of the disease. Research is constantly being done to try and make the lives of people with the condition better. Counseling is normally provided by clinics and hospitals to help patients cope.
Sickle cell anemia is an inherited disease and therefore it cannot be prevented. Such a condition is one where the patient has mutated red blood cells that are sticky and hard. These aspects often result in blocked blood flow to the organs. There are numerous symptoms and complicated that are caused by the illness. Treatments are available to slow the progress and control the symptoms. Further research is being conducted to create more remedies to improve the quality of life that patients have.
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