2 years today since I received the actual confirmation of BC diagnosis ..... I'd been pretending it was cysts up til then ...... as I walked into my GPs room, I raised my eyebrows at her & she nodded. I knew then & there it was BC.
I had a good report from my Rad Onc in early December - and I won't be seeing her again until my next MG & US next Oct .... I see my surgeon at the end of Feb, which should just be routine ...... and then check with my Onc again mid year. So far, on Arimidex I am going OK - just the odd hot flush & just now, a very sore right foot - on the ball of the foot, making it tricky to walk without a limp! grrr . Even the oils don't seem to be helping that!
SO .... I am looking forward to a better 2020 - and personally feel incredibly lucky not to have been a part of the fires when they hit our town in early November, scary tho it was, with the closest one just 500m from us. My heart goes out to all of those so badly affected by the fires - I reckon most will know someone or someone's friends who have been badly impacted. We also have members who have been badly impacted.
Take care, look after yourselves and each other xxx