Edited post: Not sure if I understand all the different types of testing...I think you can get tested (and your partner too) to see if you are carriers for any genetic conditions and then if so, they can later test your unborn baby to see if the baby has any of those conditions? Help me understand please!

Also, Did you get it done? Why or why not? Pros and cons of doing it? We just found out I'm pregnant and never got ourselves tested to find out if we are carriers for anything but thought about it. Is it too late for me and my husband to get the testing done to find out if we are carriers? Thanks!