Hi all

I am new to this forum - I have just posted in the "due Feb 16-28 2009" thread - but this thread is what has inspired me to post.

Like OceanPrincess, I had a high NF measurement (6.1) and subsequent CVS, with no sign of genetic issues. I also have twins. The initial NF US showed one looked great (low NF), while the other is/was a bit small and had the high NF. I am waiting on the 16 weeks US too, to see if they can detect cardiac issues, or maybe twin-to-twin transfusion syndrome.

Has anyone else come across any other possiblities? I hope all is well, but I was given a bit of the "ONE baby may be OK, but the other one is stuffed" at the initial scan which I haven't really recovered from...

My fingers are crossed for you OceanPrincess, and I'd love to hear how you go...