Hi Erica,
It's good to hear that you have some answers, but not so great at the same time.

I'm really sorry. How are you both handling the results?
I don't know exactly how that your RE said, explained, talk about it to you, but from my understanding (could have totally misunderstood tho) how my RE said it was that your percentages are good if only 1 parent carries the chromosomal tranverse abnormalities. That the chances of having a healthy baby is better than if both parents are carriers, but she made it sound like it is possible even when both parents have. (???) We didn't get into a huge discussion about it, but that was part of what she explained to me at the appt.
Personally I don't know what I would do being faced with this, but I think perhaps we would wait until after the genetic counsellor appt before we made a final decision and a plan. They can give you the percentages and best advice, treatment, and plan options to be able to decide from there. Any of those options aren't bad, but it depends on what you want the most... I mean obviously a healthy baby! But you know what I mean... having a sperm donar wouldn't be a bad idea if it comes down to it.