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From ball gown to theatre gown.

19 Aug

Operation number 9.  I’m hoping this is it!  I’ve made it clear I’d be happy not to make it to double figures..

You’d think after the weekend I would have slept pretty well – but I didn’t.

Here’s me sitting in admissions while waiting for my call up. This is what the Gold Coast Bulletin ran on the Pink Polar Gala.  It really was a case of ball gown to theatre gown in the space of 48 hours.

Ballgown to theatre gown

You can check out the official shots of the night from the awesomely talented Brad Wagner  As well as raising breast awareness by sharing my story and Geoff’s pursuits with the Pink Polar expedition – we collectively raised more than $70,000 for the McGrath Foundation. UNREAL!  I LOVE the Gold Coast.  A massive shout out to the little Pink Polar Committee that made it happen and a super hug of congrats to the pocket rockets that drove this event – Tess from Allamanda and Karla from ProMedia.  These two are THE BEST!

To ease the boredom of the long wait for surgery, I had my phone with me.  As it turns out, I forgot.  I was awake to be able to climb onto the operating table and remember seeing Dr D.  What I don’t remember was this….

KC Operation #9

Yes – my fabulous Anaesthetist decided to moonlight as a movie maker.  HILARIOUS!

Not long after arriving home, I put my head down.  Only to be woken by the almighty rumble of heavy machinery rolling down our street.  All of a sudden there were car doors slamming and lots of voices.  The machinery was positioned in front of the house directly opposite ours and within minutes, the demolition crew began destroying the waterfront house.  Bang, crash, creak, boom – every dog in the neighbourhood barking!  Perfect.

Demolition

 

 

Wide awake…

15 Aug

So, there’s a bit going on….

I’m excited about lots in life – Pink Polar’s going full steam ahead, I’m back writing, I’ve done a bit of media lately and thoroughly enjoyed it, I’m designing/sewing pretty well (if I say so myself), I’m back in touch with some old friends (some of whom have been around while I’ve been sick – others who haven’t) and I’m preparing for the next surgery.

Emotionally – I desperately miss some of these people and having them in my life.  But my life is not what it once was.

Two of our biggest events for Pink Polar are happening Friday and Saturday, then I have my surgery on Monday morning.  I’ve been asked about what messages I wan’t to get through to the audiences at these events.  I realise some of the critical members of my care team will be in the room on Saturday night, while others will not.  How am I going to feel standing up there in front of 400+ – just fine.  But in front of them – I hope I manage to make them proud.  To make them feel like some of the awful elements of their jobs are worthwhile in the long run – because people like me don’t waste the opportunity of a second or third chance they have helped provide.

The significance  of Operation #9 is huge.  I hope, with all of my being, that this is it now.  But – I know only too well given my serious case of de javu with the second diagnosis, to ‘never say never’.

 

I’m feeling….?

28 Jun

Okay, so I have worked in the ‘traditional’ media for the bulk of my adult life.

Earlier tonight I posted an update on social media – Instagram/Twitter/Facebook (InstaTwitFace:-) regarding the next surgery….

The amount of ‘likes/shares’ have made me sit up straight…Seriously?!

I’m pretty pleased to be at this point!!

Thank you………..KCx

IMG_2796

Consent – #9

28 Jun

Yes, well…..I don’t mention often, but Dr D was the 9th medico I saw regarding the first lump/s.  Today, we booked my 9th and hopefully last surgery.

That’s a monumental step.

I feel like I can start to breathe again.

Okay, I’ve had a glass of wine and am overly emotional, but my eyes are filled with tears and I am almost desperate for this surgery.

In Dr D’s own words ‘it’s only day surgery, we’ll go through the old scar’.  Recovery? ‘about a week’.

He filled out the details, I signed the consent.  Today is a big day.

Operation #9 is about six weeks away.  We’ve joked often in the past four years about a glass of red.  I’m allowing myself to enjoy one (& hey – I can taste it!!!), and in this virtual world I’m clinking glasses with a man who has saved and changed my life.

So fortunate……

#9 consent form - removal of portacath!

#9 consent form – removal of portacath!

Link

Tamoxifen…..

21 Jun

Another bit of ‘not so light’ reading on Tamoxifen.  Although there’s a bit in here, there’s a lot that’s not.

I’ve written about it before.

I’m still not used to this drug. Don’t know that I ever will be.

http://www.webmd.com/breast-cancer/tamoxifen-for-breast-cancer-treatment-and-prevention?ecd=wnl_brc_061113&ctr=wnl-brc-061113_ld-stry_1&mb=

 

 

‘Unfortunately’…..WTF?

2 May

It’s 2.04 am, I can’t sleep.  I’m at the computer and just clicked on a link to a story about one woman’s aim in life, following her diagnosis of breast cancer.  (There are a lot of these stories going around at the moment in the lead up to Mother’s Day).

Hoping (maybe wrongly expecting) to be inspired – I got three paragraphs in, to read ‘unfortunately  the cancer returned, this time to *name withheld*’s liver, brain and lungs, and in December last year she lost her three year battle’….

Unfortunately?!  Who wrote this?!

Unfortunate doesn’t even begin to describe this situation.

I haven’t finished reading the article.  I shut down the page with tears in my eyes and a heavy, heavy heart.

Crazy dream

2 May

It’s no secret some of the medication I’m on is really wreaking havoc with my thought processes.  So, I guess it’s no surprise that I’ve had a shocker of a dream.  You know the kind where you wake having been completely perplexed, taken aback at the imagery and confused by what it really meant?

I’d gone back to working at a radio station.  In the newsroom.  I was on-air with an announcer I thoroughly enjoyed working with in my previous life.

The screen froze – no script (what once was my worst nightmare.)

I looked up for the announcer to help, have a conversation (save me!) – but through the glass I saw a sea of faces I didn’t recognise.

They were all staring…….at what?

I looked down.  My top had slid down to reveal my bare, disfigured chest.

I’m not even going to try and analyse this one!

 

Link

Stressful – you don’t say?

3 Apr

Stressful – you don’t say?

A year since first chemo

21 Mar

Today marks a year since my first chemo.  What a different day it’s been.

I woke in a different house, with my gorgeous girls (Paul was at work bright & early), had a leisurely breakfast (I could taste!), took myself off to a yoga class and said many silent but heartfelt thank you’s.  I also spent time on Pink Polar with Geoff.  What an awesome way to ‘move forward’ as Julia (Gillard – Prime Minister) would say!

A year ago the dread of preparing for the first treatment, walking into that Oncology Unit, laying on that bed, getting hooked up to that stinky drip (ohhh the smell….it’ll never leave me), Deni giving me the ‘sex talk’, having the bizarre sensation of a destructive, but necessary cocktail of drugs etc.  I truly had no idea of the horrors which lay ahead.

I got some flowers for Dr Horwood and the team at the chemo unit.  The cards, well, where could I possibly start.  I simply wrote ‘one year on from first chemo – thank you’.

How far I’ve come, with much help.  Pardon the self indulgence, but I’m marking today with a tiny pat on the back and a quiet glass of red wine (as opposed to a drip full of revolting red chemo!).

I’m the luckiest girl on the planet.  Life, I know can be a struggle at times, but it’s good to be alive…..;-)

Curious…

1 Jan

‘Hair is over-rated’.  I’ve found myself saying that a lot this past year.  As it starts to grow back though, I’m curious as to how it will return.

Most others I’ve met who’ve had chemo talk about their new do’s, at scoring ‘chemo curls’ when they’d had straight hair their whole lives.  I had hard-to-handle ringlets, so am hoping for the opposite!  It was also blonde.  What’s starting to come through is quite dark.  Time will tell!


Hanging…..

12 Dec

Appointment with my Medical Oncologist.  As I walk into the consult room, he already has films up on the light-box and a printed report on his desk.

I’ve come on my own.

We speak about the difficulties/problems since finishing Chemo.  He asks about how I’m going with the bone pain, hot flushes, Tamoxifen……..?

I look left to the films.  Mental note – I feel like I’m hanging off a cliff….at the mercy of this disease.

There’s ‘something suspicious’ he tells me, a ‘grey mass’ in the centre of my sternum – my chest.

‘We can monitor’ he says. ‘Unless Danny has any other ideas………..?’

I have NO idea how I’m supposed to get through to April knowing there’s something suspicious.

So glad to be seeing Daniel tomorrow.  Time to do some thinking and homework.

Just a taste…

1 Dec

So, I’ve REALLY missed the enjoyment that comes with a beautiful meal.  My tastes have most definitely changed since chemo, I find I’m now going for things with a much stronger flavour, e.g. super tangy or salty sauces & dips, beetroot and carrot juice, red wine instead of white….

Diet is still predominantly raw food and organic where there’s the option.  It’s just more appealing to me to have food as close to its natural state as possible.

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Big day

26 Nov

Well..

Today started with a session with the physio, followed by a swim (with no ‘breastroke’)

I then worked with Geoff on selecting finalists for the logo design for the Pink Polar Expedition.  My goodness there are some talented designers out there!!

Then it was off to the hospital again to have my portacath flushed.  After my chemo nurse Elke took care of the minor procedure (done every 6 weeks), we grabbed a bite to eat together.  I must say how nice it was to spend a bit of time with her while she wasn’t tending to the port or administering chemotherapy!  We had a lovely chat and she was warmly supportive of the whole Antarctic idea, even wondered whether she might be able to come along as part of the support crew?!  Now THAT would be very cool!  Elke also offered to help with the fundraising.  I’ve said it many times before, people who work in this field are very, very special.

As I was driving home, the Oncologist’s rooms rang to confirm that it’s time to start on the Tamoxifen.  It was a short call, yet by the time I’d hung up I had tears in my eyes.  I’m not looking forward to taking this medication…………………………………………………………

Then, an email I’d been waiting for.  Confirmation from the McGrath Foundation that the Pink Polar Expedition is a supported fundraising activity.

Geoff is stoked too!  It’s been an eventful day for him as well.  His first full day on Mark’s ‘bulk up’ eating plan.  I had to laugh when he told me the eggs are like snot – I agree!!!  Geoff also paid the deposit on the custom-build hot pink kevlar ‘boob’ sled.

Geoff told me his last patient of the day was also a ‘breast cancer’ lady.  She shared with us a poem she wrote – ‘Granny gets her mojo back’….

So excited I’ve got SHIVERS!

22 Nov

What a week it’s been!

I’ve seen a Rheumatologist to try and get on top of this bone pain.  Cortisone injections, and all manner of other medications….Exhausted just thinking about when to take what.  I guess that’s just part of my life now.

I also caught up with a good friend who’s a journalist.  Happy to say she was enthralled with the whole concept of ‘Pink Polar’.  Knows a good story alright!

Then, a call to my dear friend at the McGrath Foundation, explaining the intention behind the Expedition. It was so wonderful to be so warmly received.  There are some incredibly special people working in this field and this lady is one of them:-)

Paul and I shared a truly memorable dinner with Geoff, his wife Sarah and children Jade, Java and Kitale.  What an amazing family!  I know I’ll write more on them in the future, but for now – my head and heart are full as a result of our time together.

A networking breakfast provided more inspiration from Steve ‘Ando’ Anderson (three-time Olympic Beach Volleyball Coach, Olympic Gold and Bronze Medal Coach) – who encouraged us all to ‘be deliberate’.  So, deliberate I was in telling him (and anyone else who’d care to listen) about this amazing project!!

The next buzz came from the McGrath Foundation – confirming interest in what we have proposed.  That’s a good thing!!  ’cause I know there are some organisations which would run a million miles from the ‘potential controversy’ a project like this could bring.  Surely they also realise our intention is good, that there are two dedicated souls involved and that my cancer experience could be used to assist in continuing Jane’s legacy (my goodness I feel presumptuous even thinking that let alone writing it – but I hope you understand what I mean).

Top off this week with a visit from Mr Hickson. Two old ‘media tarts’ (to borrow a phrase from former Qld Premier Peter Beattie [or Peety Betta as I once accidentally called him on air!]) having a good old fashioned catch up on the world.

Tired?  Yep.  Inspired? Yep. Determined? You have to ask?!!!

Ready for anything….(almost!)

18 Oct
I’ve written in the past, about how there’s now a heavy weight in my everyday, which didn’t exist ‘BC’.  It’s not to say that I was carefree, just that the realities of cancer were not the constant in my life they now are.
In a way, thinking about life beyond BC treatment is far more interesting than my safe, very structured and somewhat predictable life before.
I’m not so bothered by the fear of feeling silly, of failing or of others’ opinions.
I’m far more open to exploring new challenges, my full potential if you like.

Day of contrast…

17 Oct
What an extraordinary day of contrast.
Via text message, I learned of a difficult time being experienced by a dear friend.  It simply read; she’d found a lump, it had been looked at under ultrasound and her surgeon wanted it biopsied ASAP.
My heart sank, as my mind raced with thoughts of what the last few days would have been like for her and her family.
The emotions were very raw, as I recalled that this special lady had two years ago undergone a prophylactic double mastectomy, followed by surgery to remove her ovaries.  She has a strong family history of breast cancer, having lost her Mother to the disease approximately five years ago.
This woman has been a tremendous support for me this time around.  She’s one of the good ones and that 2.8mm lump – whatever it is – has already caused her a great deal of shock and fear.
I’ll admit to shedding a few tears for her.  With every bit of my being, I hope it’s a cyst or something inconsequential.
In stark contrast, I then went on to have an incredibly inspiring meeting with another equally impressive human being.
So exciting was this energetic chat over a plate of chicken and cashews at the local Malay restaurant, that I left wanting to yell from the rooftops about one of the most incredible adventures EVER!
More on that to come……..

Hot like radiation

1 Oct

I’ve got the song with the chorus line ‘hot like radiation’ by Gavin DeGraw on the iPod.  It’s not quite the same:-)

Submitting to this treatment everyday has challenged me (and those around me) in more ways than I can find the words to describe.

Dragging myself to the ‘radiation bunker/chamber’ every day is taking its toll.  I’ve managed to make myself physically ill every single day – despite counting down each day as a step closer to finishing this.

I’m so very tired.

I’ll spare you the detail of every day.  But here is the ‘mark up’ – tumour site, mid-line, ‘field’, the sexy gown I wear every day, some of the impact……

Psychologically – in some ways this is far more difficult than chemo.  There’s an algorithm to that.  This – ????

My mind is struggling.  My body is beyond exhaustion, my skin – so fragile – it’s burnt, blistering, itchy, hot, tender….red raw…..

The side effects?  Well, the main ones – the burn and fatigue has increased.

Fingers crossed things will settle soon…….

Farewell Bunker (thanks for the inappropriate tan!)

15 Sep
I am not going to miss heading to the radiation bunker everyday.
25 treatments with weekends off (& the odd long weekend when the engineers re-calibrate the machine) has been taxing.
The soundtrack to accompany my ‘alone time’ in the ‘Mediterranean Sea’ has included everything from Michael Buble, to Powderfinger, Etta James, Ella Fitzgerald and Kylie.
I’ve been a difficult patient.
My Radiation Therapists – amazing (Julie above & Bec below – Matt, Luke & others not there on the day I took the camera).
They’ve dealt with vomit, tears, burnt skin and moods – which at times have been not overly friendly.  We developed an understanding that, on those days where I couldn’t even bring myself to make small talk, we’d just say I ‘wasn’t feeling very sociable’.

Mediterranean Sea…

8 Aug
I’m off to the Mediterranean Sea, but there’s not a greek salad or limoncello in sight (worse luck!)
Instead, a radiation therapist presents me with a hospital gown and ushers me into a change cubicle.
This is really not the kind of sign I need right now.  I know they have to ask, but SERIOUSLY…..

From there, I enter a huge, cold room with a multi-million dollar linear accelerator sitting proudly in the centre.  I have to hop onto a narrow bed with head and leg supports, pull the gown down to my waist and let the therapists line me up.

My arms are back over my head like doing a backstroke kick drill in the pool, but instead of a board, I’m holding onto metal bars with protective plastic covers to keep things sterile.

 

As Matt and Bec work feverishly, measuring with pinpoint accuracy from the table to my new tatoos etc. – I’m silent.  In spite of much effort to stop tears, they flow freely from my eyes.  Their warmth sliding down my face and onto the hard surface surrounding my head.  As big, heaving breaths develop, I try desperately to suppress the fact I’m about to howl like a baby.  How I wished this was ending not beginning.  I have no idea how to get through this daily occurrence which will last the next five-to-six weeks.

Breathe deeply and take stock.
I’m still here.
This is helping to FIX ME.
It is quick and painless.
It’ll be over soon.
Tomorrow’s another day.  How lucky I am to have that:)

Get me out of here!!!!

‘Friendship’

19 Jul
It can take on so many different forms, huh?
I’ve written before that cancer brings out the best and worst in people.
The last six months, and in particular the last month or so has taught me a LOT about human nature.
So heart-warming it is to have some wonderful, life-long, true friends.  Being able to rely on these bonds is a lovely support.  Connecting with these people in times when I really could do with a friend, is like snuggling into a warm, comfy bed during a violent electrical storm.
I’ve also made some new friends since my first diagnosis – who I know will also be around for years to come.
The Big C, it’s obvious, is too much for others to deal with/cope with/handle etc.  Not personally – it’s me that has it, yet they can’t seem to find a way to maintain a relationship I perhaps ridiculously thought was rather important.
I’m unbelievably sad to be in this situation, with more than one person.
Devastated is not too strong a word.
I can’t make anyone care about me more than they actually do and just don’t have the energy to fight this front – I’m busy fighting cancer.