This is a very interesting discussion. For me it shows up again the variety of breast cancer treatment pathways. Seems to be affected by our different diagnoses; but specially where we live, and our public/private choices/options. Not always fair or equal.
My GP referred me straight to a surgeon after biopsy and pathology results. Lumpectomy was followed by chemotherapy and radiotherapy. I am now out in the wide world with regular monitoring appointments.
I see the oncologist who is based at the public cancer centre where I had my chemo every six months - not sure how long this will continue. Staff here have changed quite a lot. There is also a GP based at the cancer centre who sees people with side effects or other health problems. This GP prescribed my hormone medication (anastrazole) and osteoporosis medication.
I will see the radiotherapy oncologist once more in June. I will also see my surgeon in June armed with ultrasound and mammogram (yuk! - hurts!). After that I don't know.
My wonderful breast care nurse has coordinated treatment for me and advised me about what was going on.
I see my GP of 14 years for all other stuff, which luckily is not very often. She also helped me with Centrelink certificates.
Surgery was at a private hospital, and all other treatment public. All a very high standard I think.
