This is a really interesting thread and appreciate all the honesty about different decisions...kitchen sinks vs. kale and sometimes all of the above. I’ve been on this journey for 18 years, still luckily early stage despite a few recurrences, and I’ve noticed a real difference in the general attitude of the medical specialists over that time. I think 18 years ago, even before hormone receptor testing was a thing, there was a grim certainty about treatment options...you do this, then this, then this. I think now there is SO much new information, often good, that even the professionals are starting to say “it’s all changing”. It puts a bit more pressure on us as the “patient” to then try to work out options.
