Hello all, I'm new here and I would like some feedback from some of you who are much more experienced than I. My wife is a Thalassemia carrier and she has very minor symptoms that started with the birth of our first child (I am not a carrier). These are occiasional migranes and then smaller headaches. Whether nor not these are Thal related, I'm not sure but that's the extent of her symptoms.
We have 2 kids, a 12 year old with Type 1 diabetes and a 3 1/2 year old that for all intents and purposes seems very healthy. We just had a visit to our local pediatrician and our kids hemoglobin test came back at 11.4 for our 12 year old and 8.9 and 9.6 (she took it twice) for our 3 year old.
Now here is our dilemma, our ped is asking us to get more extensive testing for both of our kids. And while both my wife and I recognize that our kids could be Thalassemia carriers, we are hesistant to continually prick them with needles when they are active, have full color, eat and sleep well and from all appearances seem very healthy.
So my question to you is, should we go get our kids tested? Is childhood identification that important if no symptoms are present? If so, could you let me know why?
Thank so much