By SARAH GRANT
For the best part of the last decade, I have spent Australia Day in the same way that many 20 and 30 somethings do – having a barbie with friends at the beach or park, drinking too much, chasing the next party. It’s always been a fun day, albeit more of an excuse to stretch the hedonistic Sydney summer vibe to its full capacity than a celebration of patriotic pride.
Last Australia Day, I went to a house party in Bondi – the kind of affair that gets shut down by the police before 10pm, hordes of boozy blokes and girls clad in cut off denim spilling into the street, itching to take the party onwards and upwards. To be honest, the memory feels distant, like it belongs to a file in my mind archived long ago.
This year, Australia Day was poignant to me for reasons completely unrelated to being born in this country, or celebrating the fact. Sure, I drank a beer, I listened to the Hottest 100, I had a swim at the beach – I even chased a sizeable skink out of my bedroom. (That’s pretty bloody Australian by anyone’s standards). I wasn’t in Sydney, I was in the bush, at my Dad’s property on the outskirts of Margaret River, W.A, where I have spent the best part of three months.
Dad has advanced Parkinson’s disease and sometime midway through 2012, my sister and I made the call – we’d pack up our lives (for me that meant putting work on hold, for her it meant also relocating her husband and one year old son) to spend time with Dad.
To experience a continual stretch of time with him before his disappearing speech is lost forever, before his largely impaired mobility gives way altogether, restricting him to a wheelchair bound existence. Australia Day was my last day with him, an occasion that happened to fall on the date we raise our beers to collectively cheer our country. I toasted to my time with Dad instead.
It’s been a time of soul souring highs and heart aching lows, challenge and triumph, expression and introspection, acceptance and wonder. In some respects, I feel like I’ve learned more in the past three months than I have in the past three years. I’ve learned that life is fragile and precious, but it is to be consumed, inhaled and never taken for granted.
Top Comments
Wow beautiful post. I skip over most of the fluff on here unless I'm really bored. Posts like this are why I keep Mama Mia on my RSS feed however.
Thank you for such a beautiful story. My father was diagnosed with Motor Neurone Disease 4 months ago and I've done exactly as you have done. People often ask "how will you afford living like this?". You're absolutely right - in these life changing situations you realise how superficial and wasteful your life was. Spending quality time with my ailing father, and reconnecting with my whole family, has made me far richer than any pay packet. Light and love to you and your father.