Hi everyone,
Currently pregnant with my second child and have just come back from first scan having been told that the NT is 4.2mm. They wouldn't tell me there and then if that meant I was high risk, but I have to wait a week for bloods to be done and combined with age (35), presence of nasal bone (which there was) etc.
Have any of you had similar results? Did the combined test mean you were low risk even though the NT was high? Did you have CVS/amnio and get the all clear, but still have heart or other structural defects (which I've read can also be indicated by high NT) .
Totally freaking out at the moment. Have been struggling to get excited about this pregnancy as I'd wanted to wait a bit longer before number 2, but seeing it wriggling about on the screen was the first I'd really felt excited. Now feel like all that's been snatched away from me again.