hi NR friends, I need some support from my virtual friends.
Some of you may know from FB that I'm currently pregnant with our second child. Around 12 weeks.
We had our first scan on Monday and was told all was fine. But on Thursday evening we had a phone call from the hospital to say my blood results have shown some concerns and it has calculated that the baby has an extremely high risk of having a genetic disorder (1 in 5).
I was in utter shock. With our first we were 1 in 14000 but this time with such high risk it has really got me worrying.
We are having a private scan today with an expensive blood test done which will be able to identify if the baby does in fact have a genetic disorder, but we won't get the results for 2 weeks.
We are going to see the NHS consultant on Wednesday who has offered us to have an invasive test done where they sample the placenta to also identify a genetic disorder. The results for this would take a week, so either way we will not know for sure for 1.5 weeks at the earliest.
It's been a really really tough few days for us, as we had started telling people about our good news and this weekend I am seeing family who are being so lovely and excited for us but I am now telling them that there's possible bad news in the next few weeks.
Me and my husband have now come to terms with the situation, we are in agreement regarding what we will do if it's bad news. I do feel clear headed now and stronger, but still can't get over the shock and that we are having to deal with this - at the scan we were only going in concerned it may have been twins! How wrong we were.
Anyway i just wanted to share, not sure why, I think I do better when I am 'talking' about it tbh.
Some of you may know from FB that I'm currently pregnant with our second child. Around 12 weeks.
We had our first scan on Monday and was told all was fine. But on Thursday evening we had a phone call from the hospital to say my blood results have shown some concerns and it has calculated that the baby has an extremely high risk of having a genetic disorder (1 in 5).
I was in utter shock. With our first we were 1 in 14000 but this time with such high risk it has really got me worrying.
We are having a private scan today with an expensive blood test done which will be able to identify if the baby does in fact have a genetic disorder, but we won't get the results for 2 weeks.
We are going to see the NHS consultant on Wednesday who has offered us to have an invasive test done where they sample the placenta to also identify a genetic disorder. The results for this would take a week, so either way we will not know for sure for 1.5 weeks at the earliest.
It's been a really really tough few days for us, as we had started telling people about our good news and this weekend I am seeing family who are being so lovely and excited for us but I am now telling them that there's possible bad news in the next few weeks.
Me and my husband have now come to terms with the situation, we are in agreement regarding what we will do if it's bad news. I do feel clear headed now and stronger, but still can't get over the shock and that we are having to deal with this - at the scan we were only going in concerned it may have been twins! How wrong we were.
Anyway i just wanted to share, not sure why, I think I do better when I am 'talking' about it tbh.