Hi everyone,
Firstly sorry if I've missed a thread that discusses this or if this has been posted in the wrong place. I'm very new to mumsnet and still trying to figure it all out so please be kind 
Basically, I'm trying to see if anyone else has been in a similar situation? I'm 31 years old, currently 14+6 weeks pregnant with first baby and at my 12 week scan I opted for the combined screening. I got called back within 5 days to say that my HcG levels were high (8.18 MoM), PAPP was 1.50. So we were called in for another scan of baby.
At the scan the consultant explained that they would check the baby to see if it showed signs of triploidy, but otherwise the high hcg levels could mean that I originally had twin, had an early bleed (which didn't happen) or I just naturally produce high hcg levels. Luckily, the doctor said the baby looked normal for this stage and didn't refer me for karotyping. But he didn't completely rule triploidy out and I'm to go back to him for my 20 week scan.
I know this should be really good news, but I still can't help but panic that something could go wrong... I feel like I'm constantly looking over my scan pics to try and see if everything is okay (obviously I have no idea what I'm looking for!). Non of my mummy friends have ever heard of this so I guess I'm just looking for some reassurance from anyone else who had high hcg levels and delivered a healthy baby (obviously I know that doesn't guarantee things for me).
Thank you xx