Hi everyone, first time posting in here. At my 18 weeks sonogram yesterday they saw a “bright” bowel or a fetal echo genetic bowel. Up until now we hadn’t done genetic testing but it was encouraged today as this is a soft marker for Trisomy 21/Down Syndrome.

I have also had a subchorionic hemorrhage since 8 weeks. I went to a maternal fetal specialist at 12 weeks and I vaguely remember that doctor talking about the baby (I believe) swallowing a little blood because of that hemorrhage.

We won’t get testing results back for 7-10 days so any insights or other experiences would be greatly appreciated!