Hi all,
I'm 21 weeks pregnant. It was originally twins but unfortunately one them had a fatal abnormality discovered at the 12 week scan so I had to have a termination of the sick twin to try to save the healthy one. However, the consequence of this was that it wasn't possible to do the blood tests for trisomies. This is because of all the tissue floating around of the sick twin which is still there. This means that it's still not possible to do any blood tests so I feel still in the dark
. All I know is that the NT measurement on the healthy twin at 12 weeks was 0.9 which is very good, and that the 20 week scan has picked up no markers for anything. Actually we've had loads of scans since the reduction of the sick twin because the hospital have been keeping a close eye on things. The consultant has said that she thinks the healthy baby is low risk for trisomies.
However, I still don't feel that reassured. What if the healthy twin actually has t21 or something else and we don't know because we weren't able to have the combined tests (or any tests for that matter!) I'm just hoping that we were so unlucky with the sick twin to begin with that surely this won't happen..... Am I overthinking and over worrying?