I had an NT scan yesterday and factoring in my age (38, soon 39), nuchal of 6.7mm, and no nasal bone, my DS risk is 1 in 3, for Edwards Syndrome 1 in 2. I was utterly shocked, and devastated, as was my husband. I did a CVS right away, and tomorrow will hear the results. It is terrible waiting. Yesterday I was convinced the pregnancy would need to be terminated . . now after reading some stories of happy results, I don't know - dare I have hope?? We also opted for a DNA chip, which means even if the Trisomy 13, 18, and 21 chromosomes are okay, they will check the DNA for any other chromosomal abnormalities. Has anyone had similar experience? What was the outcome?