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What Are Cyanate And Thiocyanate Can They Be Used To Treat Sickle Cell Anemia
Ask ur Hematologist: Dietary cyanate, from foods containing cyanide derivatives, has been used as a treatment for sickle- cell anemia. In the laboratory, cyanate and thiocyanate irreversibly inhibit sickling of red blood cells drawn from sickle cell anemia patients. However, the cyanate would have to be administered to the patient for a lifetime, as each new red blood cell created must be prevented from sickling. ...Read moreSee 1 more doctor answer
An inherited blood disease causing red blood cells to be sickle (curved) shaped instead of round. It shortens life expectancy, and can result in bacterial infections, painful swelling of the hands and feet, fever, arthritis, leg ulcers, fatigue, anemia, eye damage, and ...Read more
Replacement: Anemia is basically a lower than normal number of red blood cells. If it is bad enough, it may be life-threatening because red cells carry oxygen to tissues. A transfusion fixes (at least temporarily) the problem by "filling the tank". Transfusions carry their own risks and are not treated lightly by doctors! ...Read moreSee 1 more doctor answer
See below: Sickle cell anemia can be very difficult to treat. Avoiding any known precipitating circumstance may help. Keep well hydrated. There are medications that may help if crises are frequent or severe. Blood (exchange) transfusions may also help if crises are severe or frequent. Consult with a hematologist who treats people with sickle cell anemia. ...Read more
Straightforward: Sickle cell trait is not a disease, it is a genetic mutation. In most cases it has no health problems associated with it. The only thing to be "done" for it is to ensure the person with it understands the significance that having it might have on their children. Iron deficiency responds to iron therapy; depending on the pt's age and situation tests may be needed to determine why it developed. ...Read moreSee 1 more doctor answer
Yes: In the treatment of sickle-cell disease, hydroxycarbamide increases the concentration of fetal hemoglobin. The precise mechanism of action is not yet clearbut it seems to activate of gammaglobin synthesis necessary for fetal hemoglobin. This stops the rapidly growing cells that turn into sickle cells. ...Read moreSee 2 more doctor answers
Low H/H: The most common reason for anemia in children is iron deficiency. The first step in resolving iron deficiency anemia in children is by increasing intake through iron rich foods, such as meat, poultry and fish. If this doesn't help, an iron supplement may be needed. Your doctor can help you with this. ...Read more
Can be infected: Having Sickle Cell traits doesn't actually mean that a person can't become infected w/ Malaria. But, it certainly helps with resistance. In a person who has sickle-cell trait – the red blood cells are destroyed prematurely before the Plamodium can reproduce. According to one study “Sickle cell trait provides 60% protection against overall mortality. Most of this protection occurs between 2-16..." ...Read moreSee 2 more doctor answers
None: That I am aware of.Get a more detailed answer ›
Depends: It depends on the type of sickle cell anemia. Assuming hemoglobin ss disease we recommend good hydration, avoidance of heavy exercise, avoidance of nicotine. It is really a cumbersome topic though these are the major ones. I would ask your physician, they should be able to provide you with education on prevention of sickle cell crises. Sickle cell is genetic, inherited from mom and dad. ...Read more
Sickle Cell /Malaria: In a person who has sickle-cell trait – the red blood cells are destroyed prematurely before the Plamodium can reproduce. According to one study “Sickle cell trait provides 60% protection against overall mortality. Most of this protection occurs between 2-16 months of life, before the onset of clinical immunity in areas with intense transmission of malaria.” ...Read moreSee 1 more doctor answer
Another possibility: One sickle cell syndrome is a combination of sickle cell trait and beta thalassemia. The symptoms are most like sickle cell disease. If this person had children, they could pass on the beta thalassemia and not the sickle cell. Otherwise, people sickle cell disease will have children with either trait or disease. ...Read moreSee 1 more doctor answer
Are there other tests to determine sickle cell anemia risk if my husband is away serving in the military?
Yes: The first step is testing you for sickle cell carrier status. If not a carrier then no further testing needs to be done. If you are a carrier then the next step is check the father of the baby. If he is unavailable you could have his parents tested. If neither are a carrier then the father can not be a carrier either. If they are carriers then the fathers chances are 50% he is also. ...Read moreSee 1 more doctor answer
Dietary sources: Don't forget Folic Acid either. Here is some great nutritional info: http://www.Healthaliciousness.Com/articles/foods-high-in-magnesium.Php and http://www.Healthaliciousness.Com/articles/food-sources-of-potassium.Php and http://www.Healthaliciousness.Com/articles/foods-high-in-folate-vitamin-b9.Php. ...Read more
Maybe "genetic risk: Polycythemia can be acquired. It is a natural respohse to living on a high mountain. There are oxygen censors in the brainstem and if oxidation is compromised a signal goes to the kidney to produce erythropoietin. This then signals the bone marrow to produce more red cells to compensate for the rarefied air. Exactly the same thing can happen with vitamin b1 deficiency induced by excess of sugar. ...Read moreSee 1 more doctor answer
Sickle cell anemia question. Are the blood cells normal unless there's an illness and then they sickle?
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