My amnio for high risk screening is this Thursday. I've been to a friend's for lunch today and was talking quite easily about it, now I'm wondering if I'm too calm. I think I'm in for a big shock if my baby has a trisomy.
I'm not sure if I even believe the test results. My NT was well within normal range and I am 33, so have that on our side. My bloods were high hCG and low PAPP-A, this is my 4th pregnancy and seems to be following the same pattern as the other 3 with terrible all day nausea which is now easing at 15w. I didn't have combined screening with the others so wouldn't know what my hormone levels are like normally. Also, at 6w scan the sonographer saw a tiny fluid filled sac which could have been a failed twin. They didn't look for it at 12w scan - if it was there or resolving, it would naturally result in high hCG....
I plan on telling the consultant that I'm not happy with bloods and explaining why - does anyone think it is unreasonable to ask him to scan and look at the soft markers before proceeding to amnio? I have got doubts now that actually this is a baby without trisomies and do I really want to risk a miscarriage? I will never have another pregnancy, even if I do lose this one, so just not sure its worth the risk.
Advice / comments and a hand to hold this week would be very much appreciated.
Suzy x