well ok where do i start, um ok bear with me here, im still shaking from being nervous.
Well got down there and was seen bit earlier, just couldnt sit at home going mad, the consultant was really nice, they wont have the full post mortem result back till couple of weeks, so he couldnt really comment on that much, which i could understand.
After losing chloe, i had lots of blood tests to make sure everything was ok with me and steve, (they couldnt comment on steves test results as he wasnt there) but said they had recieved them back and one of the things they were looking at was like gentetic problems.
Anyway the test they took called karyotyping, shows some abnormalities, they couldnt comment on what exactly but im being referred to a clinical geneticist to look further at it.
He said that that the chromosones affected might be to do with the baby's sex, he couldnt say for definete but could be a problem with me being able to carry girls he said that this was just something the tests were pointing too but didint want to go in to it too much, so there is a big possiblity that my first m/c was a girl but will never know.
Anyway there was no infection at all which was something i was worried about as i lost carrie-ann through infection and possibly abnormalities but didnt take any tests then.
I suppose in a way its kinda put my mind at rest and in a way its made me worry more.
But thank you all