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Thalassemia major ? truly can you die from this please help me i need to know? |
i really need to know doctors say that it cannout be treated as there is no cure but he wont die even though this is a seriouse blood disorder is this true why have i heard many peolpe die from this ? and also he is only one and had 5 blood transfussions already can he catch heb c i live in australia Your son is being treated, which increases the chances he will reach adulthood incredibly. It is true that untreated thalassemia is often fatal in the first decade of life, due to complications from the anemia or septicemia (infection). Fortunately, nowdays, it is rare for a person with it to die from it. There are some drugs that increase his ability to use iron and form hemoglobin, and of course transfusions if and when needed. Blood products in developed countries are tested for Hepatitis B and C, so the likelyhood of him getting it from a transfusion is really rare. To find out more information, check out www.thalassemia.com which will give you lots of info. It's normal to be confused and frightened, it is worrisome, and no, as of yet there is no cure. But there is treatment that is very effective and your son will in all likelyhood live a fairly normal life otherwise. You could try WebMD.com. It was free the last time I was there. Basically, thalassemia major is sort of an inherited form of hemolytic anemia which is characterized by red blood cell (hemoglobin) production abnormalities. |
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minor is supposed to be asymptomatic and not require treatment, just maintenance survaillance, you can get some information on webmd.com, familydoctor.org or mayoclinic.com, good luck ...Thalassemia is an inherited blood disorder that causes mild or severe anemia (uh-NEE-me-uh). The anemia is due to reduced hemoglobin (HEE-muh-glow-bin) and fewer red blood cells than normal. Hemogl... Check out this website ... Thalassemia Center, at Al Wasl Hospital in Dubai is considered to be a unique centre in the United Arab Emirates and in Gulf countries for the services it offers. The increase in the number of Thal... You feed this child the same thing that is fed to any other normal 9 month old. Follow the guidelines of the proper diet for the child's age. Check with a Nutritionist or your physician for ... There are a lot of differences. I apologize if I get too technical. Both are genetic disorders of hemoglobin synthesis. In sickle cell, you produce hemoglobin S, which causes deoxygenated red b... Thalassemia: Any of a group of inherited disorders of hemoglobin metabolism in which there is impaired synthesis of one or more of the polypeptide chains of globin; several genetic types exist, an... Persons with thalassemia minor have (at most) mild anemia (with slight lowering of the hemoglobin level in the blood). This situation can very closely resemble that with mild iron-deficiency anemia... |
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