Okay so my doctor is making me see a high risk doctor tomorrow because they found a couple things on baby bs heart. I can’t remember the exact work(it started with a c) but it’s a bright spot on her heart that is common in Down syndrome and chromosome defects. Then there was something about EIF

( echogenic intracardiac focus) and they only saw three heart chambers instead of four Like they did my last pregnancy with my son. I just need some more information about this and want to know if any other moms have been through this. I also went ahead and let them do the blood work for genetic testing, how long does that normally take to get back...