Hi all,
I am 30 years old and 12 weeks 6 days pregnant with my first child. We just had our nuchal translucency scan and it came alarmingly high at 5.1. The heartbeat, nasal bone and the blood results were all fine. Even though our Harmony results were clear as well, we decided to (and were recommended) to do CVS. The first set of the results came clear thankfully but we are still waiting for the second set which are due in about 2 weeks.
Does any of you have experience with the second set of CVS results coming positive? I was told that these chromosomal conditions are marginally rare than trisomy 13, 18 or 21. If these do come clear (really, really hoping they will!) they will be checking if all is well with the heart at week 16 and then later at week 20 we can finally get all clear hopefully.
I was just wondering if anyone has had the same/similar situation recently and how did it effect their pregnancies? I am happy to hear both sides of the spectrum, good or bad. It would just be nice to see if there is anyone out there I can talk to since it is difficult for other people around me to relate...
Many thanks in advance!