Hello all. I'm currently 26 weeks along with a baby girl. We are from Australia however I found this site to be most active compared to some we have here. I tested high risk at the first trimester screening with a 1 in 170 chance of my little girl having downs syndrome. (Im already a special needs mum to my daughter who doesn't have downs but another syndrome as well as being 34 years old) So far all of the scans including my 20 week morph has been clear. For awhile that reassured me until I read that some women had no signs of issues on their scan at all only to give birth to a DS child. It really doesn't matter if she does have it or not. I have one special needs girl and one other daughter who isn't special needs. So the coping with a child with extra needs isn't something I need to prepare myself for. Sort of wishing I got the NIPT now though as I feel the entire pregnancy has been nothing but wondering. Is it to late to have these extra tests carried out now? I believe my first trimester results was down to high hcg 2.835 mom the Papp a the midwife said was normal. The NT back then was 2.3mm. My other question is this is this high? I've read on the net elsewhere it can be considered higher level?
Thanks for listening xx