Hey ladies! So at my 20 week ultrasound, the doctor found three soft markers for trisomy 21. A slightly thick nuchal fold, echogenic bowel, and a dilated kidney. We scheduled a follow up ultrasound with a high-risk pregnancy doctor for six weeks later. I had the appointment yesterday. After the tech did all the measurements, the doctor came in for literally 40 seconds and said "the nuchal fold is no longer relevant at this gestational age, his colon has cleared up so physically he is fine, but we can't say anything genetically. Sometimes it just goes away. We'll make another appointment to check on his kidney, just so his pediatrician is aware." And then left. I know without any screening I can't know for sure, but I was just wondering if anyone else has this kind of experience? I had been so worried for bad news, then I got no real news.