Hello, a quick update on my daughter. I think it's good news. The hematologist said he thinks Evangelina has iron-deficient anemia and prescribed iron supplements. I was so happy to hear the news, and yet I left feeling quite strange. I didn't get the feeling he knew about thalassemia very much at all. For example he said that Evangelina's newborn screening test was worthless, because it would not catch alpha thalassemia as hemoglobin barts are not present in newborns?? When I asked if he had read the hemoglobin electrophoresis tests, he said he hadn't, nor had he read her latest CBC. He said those tests aren't reflective of any types of alpha thal? He said the only way to diagnosis even in newborns is through a DNA analysis. After I asked, he agreed to order an iron test, and then at the very end ordered a DNA analysis for alpha thalassemia. When I asked if he would take the time to read the tests, he declined and just said that my kid was obviously thriving, (can't argue with that,) and that there were way sicker kids with cancer and in need of bone marrow transplants and that I should consider myself lucky. (Also, can't argue with that.) I truly hope he is right, that Evangelina is iron deficient. But I'll be relying on the test outcomes I think.