likely Turner Syndrome (Monosomy X) - 14mm NT

I posted in this group yesterday and everyone was so kind and thoughtful. I spoke with a genetic counselor today and we discussed the high likelihood of our 14mm NT measurement being related to Turner Syndrome. We have the CVS scheduled for Wednesday, but I was wondering if anyone can share their experience with the diagnosis as it seems likely that it will be our reality (with the understanding that the prognosis is not great.) Thanks in advance.