I had the downs blood test taken at 16wks and got a call from the hospital to tell me that i was at high risk of downs 1:65. Even then this is only a 1 and a half percent chance that my little girl will be born with it.
DH and I decided not to have the amniocentesis as we are going to love this baby whether she is perfect, has downs or only one leg. And so for that reason we decided it wasnt worth the 1% risk of miscarriage to have the test.
DH said he wished we hadn't had the blood test now as it got him all freaked out but I said that if we hadn't how much of a shock would it be if she is born with downs and we had absolutely no idea??? I feel that at least it won't come as a complete shock now if she does.
When we had our anomoly scan at 19+3 there were none of the obvious physical signs of downs that can sometimes show, which put our minds at rest a little, but obviously its no guarantee that she doesnt have it.
What you need to decide is how you would feel if your baby does have down's and whether you really need to know before they are born. You have to weigh up the risks of having the amniocentesis over how you would feel about the results.
Just remember to do what you feel is right for you and your baby, don't let the hospital or anyone else try and push you into something you don't feel comfortable with. And if you decide to go ahead with the tests then you will know it is because it is the best thing for you not anyone else.
You should get some sort of counselling from the hospital, the lady I spoke to was lovely and simply went through all of the facts without trying to pursuade me one way or the other. My parents both used to be nurses who worked with people who had downs so I already knew a little.
I really hope that things turn out well for you - good luck sweetie xxxxx