I am hoping to find some answers... or comfort in knowing this isn't something I did.
During our first ultrasound, our doctor told us we had a healthy baby measuring 10 weeks, with a heartbeat of 172. We returned for an ultrasound at just about 13 weeks, and were told our little baby no longer had a heartbeat, measuring at 10weeks 5days. The doctor also told us it looked like there was thickening of the neucal folds on the back of her neck, and fluid in her body. That led us to believe she had a chromosomal abnormality.
The doctor recommended we have genetic testing done on the baby considering our age (DH-28, Me-27), and because we were past 10 weeks. We had the testing and it confirmed she was a girl, we named her Grace, but there were no known chromosomal abnormalities. It has been even harder for me once we found out Grace seemed to be a healthy little baby, but was lost for unknown reasons. Has anyone else experienced a similar situation? Could there have been other things wrong that the genetic testing did not find?
Re: Loss at 10w 5d, No found chromosomal abnormalities in baby
BFP1 12/24/14 - EDD 09/07/15 (D/C 8w1d)
BFP2 6/12/15 - EDD 2/22/16 (D/C 10w3d)
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Diagnoses and Treatments
PCOS (myo-inositol, excercize)
Indeterminant levels of APS IgM antibodies (baby aspirin)
Sub-septate uterus (hysteroscopic septoplasty 12/18/15)
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BFP3 05/02/16 EDD 01/09/17 DS born 01/05/17
BFP4 01/28/19 EDD 10/?/19 🤞🙏
BFP1 04/24/2015 EDD Dec 2015 MMC 10W5d;
BFP 2 09/25/2015 EDD June 2016 MMC 9wks;
BFP 3 03/22/2016 EDD Dec 6th 2016