I had a consultation first which was referred to as a genetic counselling session. Basically running you through what the testing does and the implications on insurance and other family members if you test positive for any of the mutations they are testing for. I got some paperwork to complete and return for detailed family history. Then once i was comfortable with going ahead with testing i was given a pathology slip to go have some blood taken. Results were given in another session about 6 weeks later. We went through the results and they made some recommendations on screening for me to pass onto my female relatives. I my case I tested negative for any known mutations but had tnbc and a strong family history of bc. Best wishes Anne