Feeling relatively ok, albeit aided by post op painkillers. Have follow up with surgeon next week to hear the pathology of 2 sentinel nodes, and discuss treatment plan. Surgeon has suggested US onco type testing - it’s expensive. Has anyone done this? Means more waiting for results (3 weeks but could be more given time of year) but potentially more knowledge and therefore better planning for chemo / radio / hormone therapy. It’s starting to sink in that this is definitely a marathon, and the surgery was just the beginning.