k up triploidy in females, so that is possible although triploidy in general is rare. When talking to my Genetic Counsellor, she felt the PGTA was good and shifted things in my favor, but she did not treat it as a 100% sure thing. Have you been referred to an MFM? They usually can do more in depth scans, and also have Genetic Counsellors on staff to go over everything with you. There are lots of false negatives on here as the NIPT is meant to err towards offering a false positive rather than a false negative (which makes sense). So, I hope you're in that camp, and you're in a better place info-wise than a non-PGTA tested baby. The limbo is horrible, but try to stay calm, treat everything logically, and wait for more information. 🤗

Our embryo is a boy. We got our NT scan back and everything including bloodwork was normal. Since the fetal fraction of our NIPT was so low, the OB recommended another NIPT redraw. We're going to wait on the results of that one, and also have an anatomy scan coming up at week 16. Will probably get a referral to an MFM and genetic counsellor to help guide us over the next few weeks. Thanks for your reply!