found out I'm a carrier of the gene for this and although it makes me so scared, I have faith all will be okay. from what I read it's very rare and not too likely that the baby will actually get the disease. as of now decided not to get dad tested just because even if he is a carrier too, that still doesn't give us a definite yes or no to baby having it and doesn't change how much we will love him. so far just going to play the wait and see game and just going to hope and pray at this point that he's born a happy healthy baby💙 anyone else go through this?