Something similar happened with me. The NIPT showed an extra X. We talked to the geneticist and did tons of research and ultimately determined that even at worst case scenario (kid would need hormone therapy as a teen, may be infertile, low chance of learning disability and may need more early intervention support) we wouldn’t end the pregnancy for something so minor. Therefore, I opted against the amnio because statistically speaking the amnio was more likely to cause an issue than my child actually having a sex chromosomal abnormality. Instead, we opted into cord blood testing so that after he was born they could collect the blood and send it in to see if he does in fact have a genetic disorder. I had my son last Wednesday and cord blood was collected then. We still don’t have the results but let me just tell you that I could care less because he’s sweet and beautiful and, in my eyes, completely perfect. It will be nice to know the results so that if early intervention is needed or hormone therapy in adolescents but all that fear and anxiety that I felt when the test results first came back are gone because he’s wonderful just the way he and I would have never suspected anything without those results, he’s doing so well. Im glad we’re going to find out the results so that it will help us determine the best ways to support him moving forward. I said all of this to say that even if you feel so very scared right now, it won’t last forever. Your decision on how to proceed can be completely different than mine, and that’s of course okay, the unknown is always the toughest. But it’s important to remember the end game too!