Hi all, just wanted to write an update of where I'm at and new questions swirling in my head. So after having a consistent ferritin level of around 30 whenever it's been testing for many years despite doing my best with iron supplements at long last I have had an IV Iron treatment! This was yesterday and I am so very hopeful it will help me achieve a better level of wellness. This was authorized by my hematologist who is the one who tested me for alpha thal.
My questions are these....
1) Even though I only have one alpha2 globin gene deletion (3.7 kb if that means anything) - meaning I'm supposedly a "silent" carrier - I do have the blood profile for alpha thal low MCV, high RBC, lowered (but not low) Hg. Soon now that the anemia will finally be addressed, it will be interesting to see whether my blood will finally look normal or not. What I'm wondering is whether being a carrier can interact with iron deficiency to magnify the impact of both conditions?
2) Looking over my DNA analysis report it says "Since this test does not detect all alpha gene globin mutations, additional testing should be considered if the clinical symptoms of alpha thalaseemia are present." At this point (unless the IV iron fixes it) I do have clinical symptoms.....is it worthwhile to push for more testing?
Any thoughts/advice much appreciated as always!