Btw I only had 3 scans all up which were dating, nt and morph scans, strep B test and GD blood test in my last pregnancy and will do same with this one so I don't think that's what you would call excessive testing. Each to their own and you need to make your own decisions based on your lives. Good luck with whatever you decide and your pregnancy!
Last pregnancy I was 30 and had no test not even measure of nuchal fold. This time at 38 I had US and combined bloods. I wish I hadn't really as I think it's only my age mostly that has give results of 1 in 212. Just in high range but really more than 99.5% ok. It's just made me feel confused. Should I do amino? Its such a hard decision! My soft markers (fold and nasal bone) were fine. Free b- hcg a just a little high and Papp A a little low so now I'm really no better than I was without test except some rules determine I am in the "high risk category"!!!! I read about so many others with the bloods three times higher than mine or 5mm folds so I wonder why I got these results!
sorry this probably doesn't help you at all! But I'd never thought of this situation...not really a big risk but a bigger risk than general population...sort of in between.
All of your comments are so helpful. I want to look at this from various perspectives, so thank you for helping with this!
Who told you the nt scan isn't very accurate? It's like very accurate! they would hardly do it if it wasn't.
Anyway it depends on whether or not you are worried if it was discovered your child had disorder. For us it was important to know so we could terminate if required and had made that decision when bub was at high risk of 3 chromosomes, all meant he he would not have quality of life and 2 meant he would have suffered terribly in which we thought would have been terribly cruel. But no one can make that decision for you, it's a decision only you can make.
Last edited by Blessedwith3boys; 11-07-2012 at 19:35.
My sister had it done, results came back low risk, only to find later in the pregnancy (28weeks, she had a scan to check placenta) that baby had major issues (missing part of chromosome 2, which is very rare) and had to terminate at 32weeks. I've had it done with both of my pregnancy.
BTW - I also know someone who had an amnio without doing the risk tests. She has a brother with downs and wanted to go straight for the diagnostic.
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