Our experience at managing hemoglobin levels of patients suffering from thalassemia
Thalassemia major is characterized by the individual not being able to produce enough good hemoglobin. This is called ineffective erythropoiesis. This condition leads to a cascade of compensatory mechanisms. First it leads to massive bone marrow expansion, unusual organs become involved in attempting to make blood cellular components, the absorption of iron from the food intake increases and consequently there is severe organ damage.