My mum is recovering from BC and has recently seen a geneticist. She has been tested and it will take 3 months to come back. The geneticist having taken a history said a genetic problem is 'likely'. 2 of my mums 7 sisters have also had BC and also a case of ovarian which is related to the BC. Apparently the average is for 1 in 9 women to get it at some stage. If she does have a genetic problem then I have a 50% chance, and if I do then DD has 50% chance too. I am not panicing or anything - my dad also has cancer at the mo and its been a real slog so I only deal in definte's and dont worry about maybe's anymore. Just wondering if anyone else has been thru this process and how it worked out for them and how they decided to address the problem, Wondering how i would address it with DD in the event that results show its positive. She is only 3 so plenty of time to consider!