I am in a pretty difficult situation, and therefore for the first time I decided to post on a blog because I really dont know who can help me. Both my husband and I tested positive for Beta thalassemia. We got HPLC testing done three time, which confirmed that we were Beta Thalassemia. I got pregnant 3 months ago and am preparing for my CVS testing this Friday. The geneticist asked us to get genetic testing to find out the exact mutation which is causing Beta thalassemia so that they could test for that in the fetus also. Unfortunately, while the genetic test showed my husband's mutation, it came back normal for me. The doctor confirmed that it happens in 2-5% cases where the sequence testing doesnt provide the results. In these cases they recommend deletion testing and even with that there is a possibility that they are unable to identify the mutation. And sadly the test takes 4-6 weeks. So I will be well in my 20th week before I find out what is going on. And if the deletion testing fails then doctors dont have any other options.
I wanted to understand, if anyone else has gone through such a situation? And what else should I be doing to expedite or really learn my mutation or test the baby for thalassemia major?