Reflections - 2 years on.
When I was diagnosed with TNBC, I was told that it was rare and the most aggressive of the Breast Cancers. It scared the crap out of me - That was 2 years ago.
When I joined this Group, it had...
Forum Discussion
Dear Mrs Doubtfire
Lovely to meet you and to read your post.
I felt so many different emotions while reading. There was sadnes and tears, there was laughter, there was inspiring thoughts and thoughts that I need to start a bucket list.
I have been through my BC journey which is done and dusted as best you can with Femara in the background and ongoing lil things from the onslaught of chemo but I am alive and kicking.
I to have been diagnosed with something "rare" and it isn't BC this time. It is called radiotherapy Morphea so I am also classed as" unique" just like yourself. Aren't we the lucky ones.
I am not quite sure what is ahead of me but your post has certainly got the emotions happening and as far as I know I should be alive and kicking at the end of my next journey.
If your sense of humour and fighting spirit is anything to go by you will be around for a very long time. Too many things on the bucket list to consider going anywhere that is for sure.
Don't ever grow up Mrs Doubtfire, we like you just the way you are.
Lots of love today, tomorrow and always, Mich xoxooxxo