Hi Kitt3n,
First of allBig hugs for you at this stressful time. I have been there with my first bubba so I know how tough it can be, least of all with two other bubs to deal with.
My DD had a NF measurement that was between 6 and 7mm. As I understand it, anything above 2mm is considered "high". When we had the combined results, our DS and other chromosomal abnormality risk rating came back worse than just the high NF measurement on its own.
Was pretty much all doom and gloom for us - we went for a CVS straight away, paid extra for the fast results, cried and agonised for 48hrs until we received the all clear from that round of tests. Agonsied for another 2 weeks for the full results, also all clear.
Agonised until 16wk u/s to check for organ abnormalities - all clear.
Started to relax, didn't relax fully until 20wk u/s - all clear.
Checked by a specialist neo-natal paed at hospital, at 4hrs, 24hrs and 48hrs old - all clear.
Fast forward to today - we are the proud parents of a happy, bubbly 15mth old with no chromosomal or physical defects at all. How was the high NF measurement explained to us? With several "it could be this" type possibilities, but we will never really know.
Now we are pg with number 2 - had a very stressful time waiting for the 12wk scan again (yes we chose to have the screening again, even after the first time) and our NF measurement was between 2 and 3mm, closer to 3mm.
Sonographer was not worried by this at all.
So I would say 3mm is not anything to get too concerned about - wait until your combined results come back.
Between now and then - stay away from Google - it is not your friend.
And then, no matter what the results are, just take it one day at a time, one step at a time.
Happy to answer any other questions you may have![]()


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Big hugs for you at this stressful time. I have been there with my first bubba so I know how tough it can be, least of all with two other bubs to deal with.

she is pretty much alright..her nuchal fold was 4mm.
ya chick


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