I had the screening and blood taken just a little over a week ago, and got my letter with the results just a few minutes ago. While I was thrilled to read that I am in the "Low Risk group," and that, "this means that the chance of having a baby with Down's Syndrome is very small," I was expecting a little more info. For example, would any of you happen to know if I will be getting a separate letter for the other chromosomal disorders the nuchal screening is meant to check for? Also, I had assumed that I would be given the actual numbers.
I suppose I should just be happy to have been given good news on Down's front, but I am still concerned about other possible issues, and, frankly, I am a bit curious about the numbers.
I've put a call in to the hospital, and I am hoping they can give me a bit more info. In the meantime, I thought I would see if anyone else had the same experience. Thanks in advance for any info.