I had my first trimester screening done today and Baby 2's nose appears hypoplastic but everything else is fine. So we have an elevated risk of Trisomy 21 and 18. This happened with my daughter two years ago and we opted to do Chorionic villus sampling then and we're going to do it again with this baby.

My daughter's test came back all clear and it was a huge relief for my husband and I.

Just wondering if anyone else is choosing to have this test done?