hello - we had our 12 wk scan yesterday with our high risk dr. Baby B had a NS of ~4-5 and Baby A was 3. Baby B also had a 'brighter' looking bowel (don't remember exact name), baby A didnt. I'm 29 with a healthy 3 year old and no unusual family history. The Dr took time to go over everything with us, but it still doesn't help that we won't have answers for weeks. She said it could be 1 or more of 3 things... 1. Chromosone disorder 2. Heart defect 3. Blood flow problems (TTTS). My husband and I are at a loss, and don't even know what to think. We are at the point where we can do a CVS test, but it's too early for an amnio. I go to my dr tomorrow for a regular check up and back to the high risk next week for another scan to see if there is any change. I guess what I'm asking is if anyone is in the same boat? I'm just at a loss and don't know what to do/expect
I've read so many stories where it was absolutely nothing and some where it ended up being serious issues.