It's lovely to be home.
Lily is being extra cautious, not to hurt my poorly boob. After an hour, I put my jim-jams on & retire to bed. Lily joins me later for a bed-time cuddle - bliss.
Then Gary joins us - heaven.
Before I left hospital yesterday my BCN told me not to waste this year trying to look too far ahead and looking for answers. It scared me. I cried for only the second time. I don't know if there was a hidden message in there - but I don't intend to waste each special moment, or even each ordinary moment. And I promise to tell those I love - that I do love them.
I know I'm supposed to be resting, but I can't resist stripping the bed - one handed of course. Put some washing in - get told off - ask Gary to carry it in for me. Everyone is being very kind.
Flowers arrive everyday - not any old flowers - some of the most beautiful arrangements I've seen - thank you my friends. And cards, and amazing messages, and texts and calls - I feel un-deserving.
It's a lovely weekend, my gang of three back together again.
One of Lily's friend's Mum offers me a life line for Monday & Tuesday. Gary wants to be off with me, but is presenting to his bosses - a preplanned event & I think he should do it. So a wonderful Mum - who I've asked to join my posse of girls (vacancies do still exist) who I may call on for help in the coming months, has Lily for a sleepover Monday & Tuesday. Another adventure for my little one - she has an amazing time. I am hugely grateful - you know who you are - thank you.
Mum & Dad come on a daily basis. My ironing's been done, and my every need catered for. Dad even pops round to put my ASDA online order away - i beat him to it of course. No goat yet - I must be ok!
I feel a fraud...I'm healing well & have excellent mobility. I'm sorted.
Roll on Friday...I want those results. I want to know which shitty path I'm destined for. And I want to know if that shitty path comes with a sticky stick too.
On the 28th July 2011, my life changed in one phone call with the simple words - 'yes - it's cancer'. I've created this blog, for the benefit of my wonderful close and extended family; and for my amazing friends around the globe, so I can keep you abreast (!) of my journey.
This will not be a sad tale - but I hope it will amuse you, inspire you, and most of all allow me to lean on you from afar, as you guide me through what looks like a rocky road ahead.
I can't guarantee a happy ending, but hope to make you laugh to the end.
My diagnosis of 2 x grade 3 (fast growing) tumours - type - 'Triple-Negative' - so called
because it doesn’t
have receptors (proteins on the surface
of cells) for the hormones oestrogen and
progesterone, or a protein called HER2, was shocking. This rare aggressive sub-type of breast cancer, therefore, doesn't respond to common
hormonal treatments, such as tamoxifen or
anastrozole (Arimidex®
) or
trastuzumab (Herceptin®
). Survival rates are considerably lower, than for more common types of breast cancer, especially in years 0 - 5, but on a par 5+ years post treatment.
Fast forward to December 2020. Secondary cancer . Triple negative again but the tumour localised to the scar of the primary cancer. The prognosis is weaker. I am buying myself time - with chemo currency.
This will not be a sad tale - but I hope it will amuse you, inspire you, and most of all allow me to lean on you from afar, as you guide me through what looks like a rocky road ahead.
I can't guarantee a happy ending, but hope to make you laugh to the end.
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