That's what you have to do. We went through moments where we were OK and felt like everything was going to be fine to the crying the next. You become a parent not when your baby is born but from the moment you find out you are pregnant. And nothing can stop you from worrying. Most of the time there is nothing wrong. Even a soft marker only increases your chances by a percent or two. Those are still really good odds.
Thank you. Just anxiously awaiting the results of the Harmony test. I'm trying to keep faith and stay positive.
Just went through something similar. We were told at our 20 weeks our little boy had a thickened nuchal fold, echogenic bowel, and an enlarged brain. Four extremely long days later we had our appt with maternal fetal medicine and got rescanned. Turns out his fold was normal, his brain looked normal, he just has a big head, and his bowel was less bright. We were told by a geneticist not to worry. We had a quad screening done and we were very low risk for chromosomal anomolies. I read so many stories where people had these things happen with multiple markers and babies were fine. Having a vsd doesn't mean the baby has anything else wrong. I won't tell you not to worry because its impossible not to, but more often than not the babies are fine. The bones are fine and your doctors aren't worried. Take comfort in that. It will all be OK.
I'm sorry to hear that. It's so frustrating. I'm trying not to worry because the doctors don't seem too concerned about it but I can't help but stress. Did you do any genetic testing?
I'm still going through it my baby is in 3-5%