Hi everyone !

At the Nuchal ultrasound - no concerns or abnormalities with baby nuchal was 1.8 and nasal bone present

At the blood test that accompany my papp-a was low and as a result had a high risk for Trisomy 18 - 1:105

Had a NIPT completed which came back low risk for everything and the doctor said it was a very reassuring result especially with no markers identified in the ultrasound

Of course she did have to remind that it is only a more accurate screen and not a diagnosis and did give me the details of further testing if I wish to go down that route

What would you do ? Or have you had a similar experience ? My 18-20 week ultrasound is upcoming in the next week or so aswell