So i know i had a prenatal screening test done at 12 weeks, but I don't know which one. I believe it was Verifi. Around the same time I had a NT scan which was normal. My verifi results were normal. I've been freaking out because i had an ultrasound at 17 weeks and an EIF was found (white spot on baby's heart) Everything else has been fine, but this has turned me into a mess. The dr is not concerned, says he sees it a lot, and he said my blood test results were good so that should make me feel better. I called the geneticist and she said my odds before the EIF for abonormalities were 1:17,000, now they're 1:8000. Big difference, but still good. I've noticed that most people seem to have their U/S first and if anything bad comes back they then go and get a blood test or amnio which puts their mind at ease if the results are good. It happened the opposite way for me. I was feeling good about my test results but now the EIF has rattled me. Do the tests i've had done matter?? I feel like i need to have an amnio or a quad. Any advice?
Re: So many tests and so confused
As for the timing, in talks with other parents who found out about chromosome abnormalities prenatally, I find I'm the exception. With the increase in prenatal screenings, it appears most are now finding out early in pregnancy. I didn't find out about a T21 diagnosis until after a heart defect was found in u/s at 23 weeks and an amnio performed. I waived prenatal screening and the NT scan , and I'm told it would have been detected at that time had I had the testing.
I had an amnio done and would be happy to tell you about my experience with it, but haven't dealt with the other specifics of your post.
You might want to consider talking to your OB about your extreme anxiety and ways to deal with that, rather than the minor EIF issue. Unfortunately it does not get less stressful or easier to be a mom once your baby is born. If you can not control your anxiety now you may struggle with all the bigger issues that can come later.