Just looking for some advice but know that ultimetly decision is mine. I'm a carrier of a genetic disorder meaning I have a pretty high chance of passing down a faulty chromosone whilst being uneffected myself. When we had our first baby (now aged 2) we were offered genetic counselling and then the options of CVS/amnio offered. We went for CVS which unfortuantley failed twice so ended up having an amnio about 15 weeks- all was fine and my little girl is now a healthy toddler. I'm now pregnant with baby 2- think about 7 weeks. Will be going for an early dating scan in a couple of weeks and then will again be offered a CVS at about 10+5 weeks. This time around I'm just not sure what to do. On the one hand I would rather know early if there was a problem (previous baby's that have been born within my family with the faulty chromosone pattern have died soon after birth due to the severity of the problem). On the other hand though I just want to enjoy my pregnancy and not have the tests at all (my husband want the test done as does not think we would cope if the pregnancy went to term and then something terrible happened)I will have the opprtunity to talk this through with the getetic counsellour but just wanted to see if anyone had any similar expereinces they felt ale to share. Sorry tis post was longer than I planned!