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The body cannot fight against sickle cell anemia, its almost helpless. It relies on treatment, an outside source to help treat the disease. The immune system does try to destroy the affected red blood cells but its not very helpful.

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15y ago
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7mo ago

The body fights sickle cell anemia by producing new red blood cells to replace the sickle-shaped ones. Treatment includes medications to manage symptoms, blood transfusions to increase healthy red blood cells, and stem cell transplants in severe cases. A healthy lifestyle with proper hydration and nutrition can also help manage the condition.

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13y ago

Sickle cell anemia can't be prevented through medicine because it is a genetic trait. The only way to totally prevent it is to make sure that neither parent carries the trait.

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Q: How does the body fight against sickle cell anemia?
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You have sickle cell anemia what will folic acid do for your sickle cell anemia?

Folic acid helps the body make red blood cells and can improve the symptoms of anemia by supporting the production of healthy red blood cells. However, folic acid supplements will not directly affect the underlying cause of sickle cell anemia, which is a genetic disorder affecting hemoglobin.


Sickle cell anemia results from a defective?

Sickle cell anemia results from a defective gene that causes the body to produce abnormal hemoglobin molecules. These abnormal hemoglobin molecules cause red blood cells to become rigid and sickle-shaped, leading to complications such as pain, organ damage, and anemia.


The difference between sickle cell trait and sickle cell disease?

Sickle cell trait is when a person carries one copy of the sickle cell gene and usually does not have symptoms, while sickle cell disease is when a person inherits two copies of the sickle cell gene and can experience severe symptoms such as anemia, pain crises, and organ damage. Sickle cell trait carriers are generally healthy, while those with sickle cell disease require ongoing medical management.


Why is sickle cell important?

Sickle cell disease is important because it is a genetic disorder that affects the shape of red blood cells, leading to pain, anemia, and organ damage. It predominantly affects people of African, Mediterranean, Middle Eastern, or Indian descent. Early diagnosis and proper management are crucial to prevent complications and improve quality of life for individuals with sickle cell disease.


Why is it beneficial to have Sickle cell anemia if you live in Africa?

Sickle cell trait provides some protection against malaria, which is prevalent in Africa. This is because the plasmodium parasite causing malaria has difficulty surviving in red blood cells with abnormal hemoglobin, such as those in individuals with sickle cell trait. This offers a survival advantage in regions where malaria is common.

Related questions

How does Sickle cell anemia affect the body?

it blocks other blood cells


You have sickle cell anemia what will folic acid do for your sickle cell anemia?

Folic acid helps the body make red blood cells and can improve the symptoms of anemia by supporting the production of healthy red blood cells. However, folic acid supplements will not directly affect the underlying cause of sickle cell anemia, which is a genetic disorder affecting hemoglobin.


What body parts are affected by sickle cell ammonia?

Sickle Cell Anemia affects all body parts as long as blood flows to that part and as long as it is prone to pain. Besides it is *anaemia not ammonia.


How does the role of a hemoglobin relate to anemia?

There is a type of Anemia called Sickle Cell Anemia, meaning the red blood cells are a sickle shape. The hemoglobin in the body doesn't work right, meaning that it blocks the vessels causing the red blood cells to break down quicker than they should, so not enough Oxygen is getting around the body.


Sickle cell anemia results from a defective?

Sickle cell anemia results from a defective gene that causes the body to produce abnormal hemoglobin molecules. These abnormal hemoglobin molecules cause red blood cells to become rigid and sickle-shaped, leading to complications such as pain, organ damage, and anemia.


Why do people with malaria or sickle cell anemia have enlarged spleens?

The spleen is the body's reservoir for blood and also plays a role in red blood cell development. When a person has either malaria or sickle cell anemia the body tries to make more blood available, so the extra amount is stored in the spleen.


What does sickle-cell anemia do to the body?

Well reag anemia is where your red blod cells produced from bone marrow are very low in quantity. Your not having enough produced. Sickle cell is the same but the few being produced are shaped diff and in a way deformed and your RBC carry oxygen throughout body so with sickle cell the RBC u do have aren't healthy and can't appropriately deliver oxygen in reag anemia they can appropriately deliv oxygen but there are very few


The difference between sickle cell trait and sickle cell disease?

Sickle cell trait is when a person carries one copy of the sickle cell gene and usually does not have symptoms, while sickle cell disease is when a person inherits two copies of the sickle cell gene and can experience severe symptoms such as anemia, pain crises, and organ damage. Sickle cell trait carriers are generally healthy, while those with sickle cell disease require ongoing medical management.


Can anemia lower your ability to fight off infections?

Anemia affects red blood cells usually, and doesn't always lower the immune system response but aplastic anemia (a.k.a bone marrow failure) causes the body to produce less red blood cells, WHITE blood cells, and platelets. Therefore, I believe, anemia can lower your ability to fight off infections (if the amount of white blood cell production is lowered). the above answer is true but people with sickle-cell anemia have a greater resistance to malaria. Also aplastic anemia patients have just as much troube as fighting a VIRUS as any other person.


What kinds of anemia are there?

The different types of Anemia include: . Iron Deficiency Anemia - Is causes by blood loss, or lack of iron in the diet. . Pernicious Anemia - It occurs when the body is unable to absort Vitiman B12 . Folic Acid Deficiency Anemia - It occurs when there is a lack of folic acid in the diet. . Hemolytic Anemia - It is an inherited or acquired type of anemia that causes the red blood cells to be deformed, so the body breaks down the red blood cells too fast. . Sickle Cell Anemia - Inherited disease that occurs when the red blood cells are sickle shaped. The hemoglobin doesn't work right, the shape of the red blood cells causes them to clog the blood vessels and break down easily.


Why do the attacks of sickle cell crisis increase in high altitude?

The main reason that attacks of sickle cell crisis increase in high altitudes is oxygen. When the body lacks or needs more oxygen, it makes the body work more to get it, thus causing the crisis. http://www.nytimes.com/health/guides/disease/sickle-cell-anemia/print.html


How can one avoid macrocytic anemia?

Macrocrytic anemia is usually caused by poor nutrition. Getting a sufficient amount of vitamins, especially B12 can help your body fight off macrocrytic anemia.