NT scan was last Thurs. It's not looking good. Looks like at least 1:2 chance of chromosomal disorders, 5% chance of a live healthy baby surviving more than a few days at most.
If anyone has any stories of beating the odds (and the cystic hygroma is considerably more concerning than the NT measurement alone - DD was also >95th centile for NT and is absolutely fine), then please tell me.
Or if anyone's been in a similar situation and can advise what questions I should be asking/tests we should be requesting/things we should be thinking about, again please let me know.
We have an appt with a consultant in fetal medicine on Thursday, one with the high-risk obstetrician on Friday (had been scheduled before the NT scan due to other factors) and a cardiac scan/assessment next Monday.
I turned down CVS due to the risk of miscarriage (I know, risk of miscarrying naturally is far greater - but whilst there's still a 5% chance of a healthy baby I'm not going to jeopardise that). I'm already 14w1 anyway so we wouldn't have long to wait till the lower-risk amnio became an option if we wanted, so didn't see the point in rushing to squeeze in a CVS - especially as we can get the cardiac scan in the meantime.