I wasn’t sure if I wanted to post this, but I’m in need of emotional support. I did a nipt test at 10+5. It came back negative for all except for monosomy x( Turner syndrome). It’s a 33% chance my baby could have this and I’m terrified. There’s a high miscarriage and still birth rate for this genetic disease. I do have a bit of hope because of the 33% chance of the baby having but also, in everything I’ve read about nipt testing, they say they require at least 4% of fetal dna in your blood for it to be somewhat accurate. I only had 3% fetal fraction. That information alone has give me and my SO some hope. In 2 weeks I have an appointment for an amnio draw to determine if my baby really does have Turner syndrome. I just really need some insight and encouraging words. Thank you.