On the day I had my NT scan at the Perinatologist's office, they also took bloods (12w0d) and told me that I was getting a Triple Screen for chromosomal abnormalities. I basically HATE the idea of all of these "probability" tests that could introduce unnecessary worry or force decisions like having an amnio or not. But I decided that it's the responsible thing to do to get all this checked out so we can be prepared at delivery if there's a problem. And my insurance totally covers it...

Well my NT was great, and I never heard back on the 12w b/w. Is this normal? I have to go for my 2nd round of b/w this Fri @ 16w...Do they compare the 2 sets or something? Obviously, I am getting nervous bc this b/w is the last hurdle.

I haven't had to worry about anything in a while, so I guess I'm focusing on worrying about potential problems with this now...

Did you have the triple screen? If your NT scan was ok, was your b/w pretty much the same outcome? I'm starting to sweat!