I'm from Canada so some things are differnt then what most of you are doing in America, so if your Canadian please add your two cents and if not I would still like to know what you think.
After talking to my dr and finding out the our MSP doesnt cover the NT scan but does do the blood test but is optional and a whole bunch of information was given to me about it. After going home and thinking about it I am unsure weather I really want to take the test and know or not.
Reasons for and against are
1: If i take the first test I dont get results until after the second blood test at around 20 weeks where they will tell me my risks however at 20 weeks we have an in deapth scan that also checks the NT from what I remember so is it better to have both?
2: its common to get false positives so do I want to give my self un needed stress which in turn can halm the baby?
3: either way we will keep the baby so the results wont change that
4: knowing at least helps us be prepared for the forth coming of a special needs child
5: if we get a positive the next step is amnio (sp) which can cause mc but I know I wont take that test to confirm so am I simply wasting time and un needed stress as well as government money just to find out something that wont change our outcome but simply prepare us.....
so now im on the fence im thinking over all it may be best not to know and now I have a headache anyway any thoughts or experiences from anyone with a positive that really helped them prepare or with false positives that simply stressed you out and caused complications or those that got negatives and are happy to know so they dont have to worry about it any more.
All thoughts would be great
Thank you
Re: NT T18/13 etc test ? long
Are you high risk?
Not sure of your age, etc., but my doctor told me, for example, that since I'm 28 and have no family history of Down's Syndrome (on either side), my risk of having a baby with Down's is about 1-in-900.
She said if I have the NT scan and blood test and everything looks good, then my risk of having a baby with Down's drops to 1-in-10,000.
It's all a probability game anyway; there are no guarantees. (Maybe there are with amnio, but not with the NT scan and corresponding bloodwork.)
I'm not Canadian but I wanted to respond with some food for thought:
Thank you for your response it will help in deciding what we are going to do,