Anyone here have clear genetic tests after abnormal results but then went on to have anatomy issues?
At 9 weeks I was told that my baby had skin edema and thickened NT which appeared to be CH. Measured around 2.2. Fast forward to 11 weeks both had resolved. Since then my CVS, microarray, and kareotype have all come back fine which has been a huge relief as I’ve been incredibly stressed. Early anatomy scan also came back fine. I’m now at 17 weeks and waiting for my anatomy scan and fetal echo around 20/21 weeks. Has anyone been in my situation where everything was cleared and then they still structural/heart issues?
Although I’ve been feeling relieved, I’ve been guarding my heart in case something shows up. We have kept this pregnancy private from our families but it’s getting harder to hide and I’m just ready to share but scared that something’s going to come back wrong - it would break them and me too 😔