Well, the baby had a thickened nuchal measurement. It was 2.5 or 2.6 mm. I'm kind of still processing. The doctor said that it was a cause for concern, and he recommended we just go ahead and do the Harmony test, which looks at chromosomes 13, 18, and 21. So now we're waiting ten days for results.
He said that even if the chromosome testing comes back with no trisomies, we will still need to do a high-level scan of the heart at 22 weeks because the thickened NT could be indicative of a heart defect. And I guess there could also still be chromosomal abnormalities that don't involve the three main ones they look at.
I'm a worrier, and I was so worried during my first pregnancy about this kind of thing. This time around I've been a lot more laid back. I don't even know what to think right now. Nothing to do but wait.
Re: Not a great NT ultrasound
BFP #1 : 3/20/13 | EDD: 12/1/13 | MC: 4/15/13
BFP #2: 1/9/14 | EDD: 9/21/14
Welcomed our rainbow bear on 8/31/14
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Oscar born October 2011
Miscarriage at 8 weeks (August 2013)
DD due September 1, 2014
First BPP 1.24.14
EDD 9.26.14
Baby Cooper John born on 9.24.14 6lbs9oz
BFP#1 4/17/2013 EDD 12/25/2013, MC 5/17/2013 8 weeks 3 days D&C 5/18/2013
BFP#2 1/20/2014 EDD 9/28/2014, Baby Evie born on 9/23/2014 at 8:50pm. 6 lbs 15 oz!
First Son - born 2013
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#2 04/17/09-Boo-kie C-section
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Gemma
born August 31, 2014
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