Conquering change.

What it really meant to finish chemo

“I conquered this moment”. That’s the sign on the wall of the chemo clinic above a big brass bell to represent whatever people need it to represent. Most of the time, the ringing of the bell is about celebrating the last chemo session ... But for me on my last day recently, it felt more like an apology than a party. Like I should have been standing at a private wake rather than a public celebration. There was an applause and cheer from the nurses and even the patients. But I just went back to my hospital chair and cried quietly while I packed up my bag and walked away. 

I thought I'd feel elated, excited, proud. I thought I'd be breaking out the Hawaiian shirts and pina coladas and balloons. That the only heaviness I'd feel would be from the world boxing champ belt that I would have otherwise been wearing after going 12 rounds with chemo. But the heaviness was on my heart (and my backside from the weight I've put on in the last few months). 

I did feel proud that I had come through all of this (relatively) in one piece, but I realised it was much more than finishing chemo. 'This' was really about the last six months since diagnosis when my world decided to flip on its own axis.  I was also just unsurprised by it all... Did I ever give myself permission NOT to get through it? Was there ever any other choice I offered myself? Well, yes there was. I could have put on the pink boxing gloves and taken this all on as a fight. I could have pushed back in denial. I could have allowed myself to become victim to my anxiety about all the things that could go wrong. 

But I didn't. I surrendered to it all with the perspective of treatment, not toxins. I surrendered to the facts like I would lose my hair and that I would have some really crappy days. What I also did was trust. I trusted that there were medical experts who deal with people like me every single day.

I also trusted myself. I have come to realise the hard way that the strongest and most reliable friend I had in all of this was me. And when I say me, I really mean my mind. The messages I tell myself. The choices I make for myself. The decisions I commit to that are about looking after me. Sometimes those decisions and choices have been to shut out the noise of the "should" list and instead spend a morning in my linen cupboard throwing everything on the floor and creating a new colour-coordinated Tower of Towels. And sheets. And cushion covers. And crap I didn't even know was in there (And who can really make those damn fitted sheets have square edges!?). Sometimes it's not answering a phone call because I'm simply too tired/brain-fried/wired to try and string two words together. 

I couldn't tell you what I've done in the last six months. Sometimes it feels like its been one continuous day. People keep asking me though so I've started to think a bit more about a better way to answer it other than coordinating linen cupboards and binge watching house renovation TV shows. 

What I've done is lived. And the last six months is really just a snap shot in time of a life. A life that could belong to anyone. I've done whatever I've had to do to survive. And I don't mean from a life/death perspective (even though it's in the context of a life-threatening disease). I mean to survive each day by nurturing myself enough or asking for help enough to know I can get up the next day. 

I have grieved so many things - lost plans, lost opportunities, lost choices, lost identity, and lost confidence. 
I have persevered with love and compassion in the face of bitter brutal disappointment from people closest to me who were never supposed to know how to deliver such blows. 
I have suffered pain, fear, hurt, anxiety, sadness, grief, anger. 
I have surrendered, fallen over, laid down naked, and not gotten up. 

But I've also received with absolute clarity the gifts of trust. Of kindness. Forgiveness. Openness. Vulnerability. Hope. Love. Laughter. Courage. 

I have honoured myself, my life, and the choices I’ve made.

I have embraced all the unknowns and all the choices I still have in front of me.

I have heard quiet for the first time in a long time. 

I have given myself permission to shred the Should list(s) and replace them with Today I think I feel like...lists. 

And above all else I have evolved. I have changed. Pain had gifted me that.

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Taxol, not Taxidermy!

Embracing ‘Slow’

All aboard the chemo go-slow train! It’s one of the most frustrating (but comical, apparently) side effects – chemo brain fog. I was told at the beginning of treatment that my ability to think, multi-task, focus on details, remember stuff, was basically going to be on the ‘wish list’ for a while. That instead, chemo causes the brain to malfunction a tad. My panicked face was because I surely need to do all those things for a living!

But these days, I ‘wear’ a banana, rather than ‘eat’ one. I write my birth date on consent forms, rather than today’s date. I announce that I’m at the chemo clinic for taxidermy, rather than taxol (the name of the drug)… that one had the nurses in stitches.

I’m now embracing it like everything else about chemo – a chemically-imposed trial of SLOW. There are books written about it and workshops and experts teaching us how to de-clutter our lives and, by extension, our heads. It’s about moving slowly, eating slowly, breathing slowly, and thinking slowly so that we all have more time to reflect and ponder and immerse ourselves in the present.

While it is a confronting thing to be shooting blanks at the most basic of conversational times, I am trying to see it also as a way of my brain (and body) taking some well-earned long service leave from what has otherwise been more than 20 years of frantic busyness where my brain didn’t know how to switch off and just ‘be’. I sometimes wonder whether it was an inconvenient truth to not want to do it either.

Becoming disconnected from the world of emails and meetings and ‘busy’ has made me start to ponder how, in a world of instant connection (with devices), that we are so disconnected (with people).

In among the many not-so-great things with this year of diagnosis and treatment, I have been gifted with Time. It can feel like pure self-indulgence. I then question whether I should be doing something more constructive like solving world hunger than going for a walk to my local coffee shop and talking to random people. But selfishness is not a dirty word for me anymore. It’s instead another word for self-preservation.

When I see someone now getting lost in the excitement of their phone’s notifications, I want to scream “Just look up!” You never know who or what you might see right in front of your face. There’s sunlight. Trees. Birds. A big blue sky. Oh, and those unknown scary creatures called people. If you’re lucky, you’ll have a moment of connection with something that doesn’t require a battery recharge. 

I see it with kids too, where ‘fun’ becomes the conjoined twin to smart TVs, playstations, and wifi. What about a 5 minute walk to the beach. The wildnerness. The wonderment. The “why” of life. 

So I’m going to enjoy riding the go-slow train. In fact, I’m not sure I’ll ever get off it. It’s time to welcome some empty space into my head so that I can make more room for new stuff, new friends, new experiences, new dreams, new perspective. And ultimately, a new life.

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