Can anyone please explain the first trimester screening tests to me as I feel I am not bring given a full enough picture by HCPs?
Firstly is the nuchal just to assess the risk of Down's or can other chromosome abnormalities be detected with the NT? And if so, what exactly are these conditions?
Secondly, the serum/blood tests - exactly what can be picked up by this, as well as Down's? I have read that many factors can 'affect' the result, some of which apply to me (being very slim and having T1 diabetes) - but what does that actually mean? Is being light, for example, a real risk factor or does it lead to false positives for some reason?
However, my consultant told me that diabetes does NOT affect results, but I am beginning to suspect she is trying to get me to have the screening when I don't really want to.
I'm really confused. I do understand the the serum screening and the NT don't give a definitive answer - I don't understand what may be picked up aside from Down's and how the risk is calculated.