Hi all! So we recently found out that both my fiance and I are carriers of Cystic Fibrosis. Meaning our little one has a 25% chance of having it. I know it’s a small percentage, but having that now hang over our heads is not the best. We see a genetic counselor this week and will find out more. I just wanted some input and thoughts from others out there who maybe went through something similar and if you had a CVS or an amnio. Any advice helps! Thanks!!