Always wear the sparkly shoes; a life lesson

Ruby Slippers from the Wizard of Oz

Here’s how my daughter Zoe and childhood cancer taught me not to wait til tomorrow to wear the sparkly shoes.

At the beginning of 2012, Zoe was excited to be going to Camp Quality, a camp for kids living with cancer. One of the activities planned was a dress up party based on movies. Zoe and her camp companion were going as Dorothy and the good witch Glinda from The Wizard of Oz.

We looked all over town for red sparkly shoes to serve as Ruby Slippers for Zoe’s Dorothy, but there were none to be found. We had to decide what was most important – red or sparkly. “Sparkly” was Zoe’s unequivocal answer. Continue reading

One thousand and ninety five days without you

all the ages you never got to be

Three long years since you left us baby girl. You would now be entering tweenhood, but I find that so hard to imagine. The little girls my eyes always linger on are the ones that are all the ages you were, not the ones you never got to be. The toddlers wearing gumboots and tutus, pre-schoolers wearing glittery star t-shirts and choosing buns covered in sprinkles at the bakery, gaggles of giggling six year olds.

Some days, when something jogs a forgotten memory, or a photo unexpectedly brings a rush of emotion and I can recall the exact sound, smell, touch of you in that moment, I feel so close I could almost touch you. Other days I feel I am drifting further from you, despite hoarding memories, photographs and all your possessions. Continue reading

The Princess Manifesto and other Zoe-isms

I don’t usually write posts based on writing prompts – I just write when I feel the inspiration (bad blogger). But today I saw a prompt that was one word – handwritten.

Co-incidentally, after a discussion with friends about wedding dresses, I had been thinking about something Zoe wrote in a card to me. It was around the time of the royal wedding and all the little girls at her school were obsessed with weddings, so I showed Zoe the photos of my wedding to her Dad. Disappointingly for Zoe I had neither a train on my dress, nor a veil on my head. However the photo that fascinated her was the one at the top of this post, because it was all about her, a 32 week post conception Zoe in mummy’s tummy, in a wedding dress, inspiring her to draw me a picture and write me a card with these words in it. Continue reading

How to guard your heart

The other day I was telling a friend that I thought the heartbreak songs he had written were lovely. It was the third anniversary of Zoe’s terminal diagnosis, and when I told him I was listening to more heartbreak songs that evening because it suited my mood, he replied that he hadn’t written any songs that heartbreaking.

That exchange got me thinking about how often people tell me that when they think of Zoe’s story, it puts their own troubles into perspective. I get that, and I know it’s been a life lesson for many people whose lives Zoe touched. It certainly helps me to put everyday disappointments and dramas in their place. Aren’t we all learning over and over not to sweat the small stuff? Actually if you have this completely figured out – please let me know 😉 Continue reading

Three years ago today

It’s that time of the year where every day I think about what we were doing three years ago today, in the days leading up to Zoe’s relapse and the last few weeks we had with her before she died. I think about it in vague terms because I didn’t keep a diary, just posted a couple of random blog entries and I have never gone back and looked at my facebook posts from that time.

But earlier this year I unthinkingly activated facebook memories. Now I am getting daily reminders of what I was thinking and doing on this day last year, the year before, and the year before that. Continue reading

The labels I will not own

“Above all be the heroine of your life, not the victim” – Nora Ephron

A few months ago, someone I had met just recently told me he thought I was fragile. In the context I don’t think they meant anything negative by it, and yet I was taken aback, and I’ve thought about it a lot since.

Not only is this not how I see myself (at least not these days), but I had deliberately chosen not to mention “my story”, as I sometimes choose with people I have just met precisely in order to avoid this type of response. The pity in their eyes, the frantic scramble to find something appropriate to say, the labels they attach to me, that I am Brave, that I am a Victim, that I am Permanently Sad, that I am some kind of Tragic Heroine because my daughter died. Continue reading

Random thoughts on cancer, meaning and happiness Part II

“Hope is not optimism, nor is it conviction that something will go well. Rather it is the certainty that something has meaning…regardless of its outcome.” Vaclav Havel

From where I stand now, I feel I can truly say that life (for me anyway) is not about happiness, at least not in the ways it’s most commonly perceived to exist. Rather it is about finding peace and meaning. That doesn’t mean that I don’t feel any joy or happiness, but that I find those things through the meaning I attach to my life and experiences. Continue reading