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Shiny & New

29 May

Although these implants are slightly bigger (545’s as opposed to the old 485’s), they don’t actually feel it – thanks to the new position.

Having said that, my skin is so stretched it resembles a balloon ready to be popped by a pin! (Mum laughed at the way the flash bounced back at her when taking this shot..)


This was taken a week after the surgery. As for the rest of me, I’m feeling quite nauseated at times, am tired and have already had enough of asking for help with the basics.

I could change the tape here at home before seeing Dr D and Andrea on Monday, but as far as I can see (through the tape) the scars appear to be healing well. Although I’m keen to see them and start getting used to them, I’m also happy to leave the dressing changes to the experts (I’ll be on the betadine and fresh tape routine again soon enough).

Frustration..

28 May

People are often surprised at some of the basic things I’ve found difficult after each surgery, so I thought I’d list some for you.

For this op and the last reconstruction, the restriction of movement is definitely top of the list as far as frustration goes – one wrong move and my chest is burning with nerve pain as I try to hold back tears that seem to come from nowhere. It really stops me in my tracks.

Some of the other things are so simple they’re kinda funny;

  • holding the phone up to my ear for more than a few minutes – amazing how quickly my (big strong) muscles tire,
  • grabbing something from the fridge/pantry (& even soap/shampoo in the shower) – the essentials all have to be at waist-shoulder height (needless to say any chocolate etc. has been safely stored where I can’t reach it!),
  • showering – making sure soap gets to all the right places can be tricky (ohh – & shampooing my hair resembles some sort of contortion act as a bring my head down to hand-height!),
  • drying myself – getting a towel around my back (especially if it’s already wet and heavy) – not easy,
  • sitting up straight for long periods of time – after a while the blood pumping to my chest region (particularly around the new scars) really starts to hurt in a way similar to one of those throbbing headaches,
  • getting in to & out of the car – pushing and pulling of any nature, especially your full body weight, is out of the question.
  • getting in to & out of bed – same as above, blood rushes and no twisting around or pushing/pulling to prop yourself up or help in any way,
  • cutting up dinner – steak (no matter how tender) is off the menu for a while!
  • lifting a full kettle of water – when anyone drops in for a cuppa it’s not BYO, but pour-your-own,
  • this only applies to the first fortnight after surgery, but those compression stockings are bloody hard to get on at the best of times, let alone when you can’t reach forward very far and are a bit weak. Not having to wear these will mean I can have a bit of independence back, but for now I have to ask for help before and after (& okay sometimes during) every shower. Uurgh.
  • Clothing – it has to button up down the front, or be something (like pants/a singlet top) that I can step into.

In short – when Dr D says ‘you should be right with everything straight in front of you’, he’s right.

It’s still early and I know from past experience that these things become less of an issue with each day. Thank goodness! ‘Patience & Tolerance!’

It’s 3am, I must be lonely…

28 May

I’m not really -but you know the Matchbox 20 song!

I just can’t sleep – equal parts pain and nausea. I can’t think what’s making me feel sick, other than the pain. Vicious cycle huh?

So – seeing as it’s 10 days now since my last op, the heavy duty pain relief has ceased. I’ve come downstairs popped two Panadol and two ginger tablets to try and settle my stomach. With a chest full of stitches, the last thing I wanna be doing is vomiting. Come to think of it – coughing and sneezing are also pretty high on that list, so keeping warm is also a priority.

Patience & Tolerance..

28 May

That’s a saying I heard repeatedly as a child and one my Mum actually hasn’t had to use all that much during my little ride.

Almost by default (you know – having to endure a range of procedures which often involve long, sometimes painful waiting periods), I’ve become a lot more patient in certain circumstances. Like when Paul’s driving and we get a red light now, I just shrug my shoulders as steam blows out his ears. I just don’t care, it’s no big deal. (Truth be told I’ve actually found his impatience stresses me out more than the situation.) Another example is when Mum’s had a bad day and the issues come spewing out of her mouth as she walks in the door. Although irritating, fortunately none of them are overly life-altering. So again – I just shrug my shoulders. Not being rude – but those little things, just don’t matter in the big scheme of things.

As far as my tolerance goes, well it has changed too. To put it bluntly – I’m far less tolerant of things that don’t work for me. If a shop assistant is rude, or say we go to eat somewhere and I don’t love the look of something on the menu – I just walk. No offence intended, I just make that decision and act on it, rather than being polite and staying because I feel obliged to. It’s just – bye! On a positive – I’m far more tolerant of people whose individual situation might dictate their behaviour. I’ve found myself stopping to really listen and give consideration to what the reasons behind certain actions may be.

This experience has most definitely brought to light some different examples of patience and tolerance.

Home again..

24 May

Although Dr D would have been happy for me to go home the following day, my ‘roomy’ and her groaning (did I mention she also had a needle phobia which prompted some blood-curdling screams in the middle of the night?), had me feeling less than energetic as he did his rounds.

Anyway, I stayed for a second night and felt 100 times better 24hrs later.

The short drive home was again, well, excruciatingly painful is the only way to describe how my chest felt as we took each turn and thumped over the unavoidable bumps in the road.

Geez, there’s nothing like having a shower in your own surrounds. I may not look happy – but I really was!

So, the supportive taping is obvious. The implants are certainly more ‘front & centre’. My new scars as you can see are underneath (Ohh – those purple lines down my sternum are Dr D’s pre-op artwork, still to be scrubbed off), and the old ones are a little stretched but still intact! There’s just a bit of bruising, but it’ll go.

Nursing Conference – me!

24 May

I keep saying ‘who would have thought?’ – here’s another example of why;

Here I am manning the display on behalf of Cancer Council Queensland at the recent Australian Practice Nurses Association conference held here on the Gold Coast.
Yep – spent the day talking about all kinds of cancer, to all kinds of people. Sure, the majority were nurses (which was interesting in itself), but I also had the opportunity to speak with colleagues from Cancer Council NSW and Victoria, researchers, Dr’s and other health professionals (even health reporters! funny..).
Little old me, out there in the real world after spending so long behind a newsdesk reporting on things.

The Funny Little Things..

24 May

By now I figure I don’t have to apologise for my warped sense of humour – you’ve already been exposed to enough examples of it.

Having one certainly helps. While going through my obs with one of the nurses – I got a serious case of the giggles at the third item on the list;

 

 

Yep – that’s right – N/A because there are no nipples! Ahhh…geeez..hurts to laugh..

A Little Too Eager..

22 May

Seems I got a bit excited. The bra was yet to come.

Later that evening Dr D popped in to check on things (looking like he could do with a very strong coffee to get through the final surgery he had to perform for the day..I mean that in the nicest possible way of course!). He seemed surprised that I’d been up and showered and sternly instructed the nurse to ensure the waterproof dressing was put in place asap (oops..).

He put some big strips of supportive tape along the outside edge of my right breast, pulling things into the centre rather firmly. As Dr D flew back to the operating theatre, the nurse taped up the other side and helped me get into the zip & buckle up bra.

It was getting late. I was left with my oxygen, push button pain relief and a flimsy curtain separating me from my not-so-well-mannered neighbour who moaned throughout the night. Ohh – she also felt it necessary to make demands on the nurses each time they popped in for the two-hourly obs ‘get me morphine’ she bellowed….. It was a long, looong night.

‘Breast’ Buddies..

22 May

After being so rude in my previous post – I’d better show you that we really are the best of friends.

Transformation

22 May

I woke up this time with no drains and no compression bra! Just oxygen, pain relief, fluid and antibiotics.

Already I could feel the implants were more central on my chest and my sides/underarm area felt more familiar. Whew – two hours and it was over.

 

Of course Little Miss Impatient was desperate to brush her teeth and have a look in the mirror. The nurses said they’d give me a hand to shower, but that wasn’t necessary. (I was still flying!!)

What would I do without my snap-happy friend Sum? Having been away for my first four operations, it was a real treat to have her in my hospital room when I woke from this one. But I ask you – what kind of friend enjoys not only paying out on me looking like some kind of weird, not-so-sexy french maid, but also going to the effort to record it?!
Seriously – thanks Sum. x

Operation #5

18 May

This is the body (and boobs) I said goodbye to a year ago.

Now, here I am having had the mastectomies and reconstruction – going back in for another round of – as Dr D likes to put it – ‘tweaking’. (I get the irony on both fronts – as a dear friend pointed out – the only one who should be tweaking is my hubby and the reality is I have no nipples to tweak!)

Not only was I not sporting the gash-like mastectomy scars then, but I’m about to score another two, underneath.

One of the aims of this surgery is to try and disguise the obvious divet which angles its way across the left side.

 

Another is to position the new implants in closer, level them up and try to reduce the rippling..

See you on the other side..

Mother’s Day 2010

15 May

Last Mother’s Day was pretty emotional, as I was just a few days out from my ‘big op’.

This one, was quite different. We celebrated a little early with High Tea at Keri Craig Emporium in Brisbane (for those of you who agree that I was born in the wrong era – here’s proof!), we had a lovely time.

The Sunday of Mother’s Day, we – along with thousands more around the country, joined in the Mother’s Day Classic walk/run, raising money for the NBCF.

While I walked alongside Paul, my Mum, my sister Kristi and friends Wayne and Susie, pounding the pavement beachside on the Gold Coast, my dear friend Summer and her sister Jayda did the walk in Sydney – in memory of their Mum lost to breast cancer 20 years ago.

…and again.

13 May

Yep, next week will be round five.
Explaining this could be rather detailed – but in short, these implants are coming out and new ones are going in. In fact, the consent form says ‘remove and replace implants’.
I’ve been in two minds about this for a while now. As you may recall my ‘adjustment’ to this new body hasn’t been as smooth as I would like. Not long after the reconstruction Dr D cottoned on to this and said we could go back in and try and refine things. I very quickly snapped no, that I’d had enough surgery and I just needed to let my head catch up with what the body has been through. I’m almost ashamed to admit that unfortunately (not for a lack of trying), that hasn’t happened over the past few months.

A recent appointment brought the issues to the surface. Try as I might to just suck it up and well, not love – but just feel good about things, I couldn’t. Don’t get me wrong – I’m incredibly grateful to be here and on most days view my scars almost as kind of battle wounds, that through them – I’ve been given the best chance at a long and healthy future. It’s actually not the scars. The position, shape, ripples, distortion and an unsightly divet of my new ‘breast mounds’ are taking some getting used to. (This all sounds so much worse than it is!) Most of the time I’m okay, but occasionally it all is too much. The disbelief I feel is enormous.

I’d been keeping my mouth shut, so as not to offend Dr D. This was his work – he’s worked so hard to re-build me and here I was not handling the end result. How dare I? What an ungrateful sod.

He’s most perceptive and as I removed my gown he started with ‘we can do this, this and this….’ I was so relieved, I got a bit emotional and nearly cried (after all of this – it’s the first time I’d come close and I didn’t want him or Andrea to see me cry!). In a very business-like manner we talked about the ‘tweaking’ as he called it.

On leaving, Dr D reinforced that it’s okay, they often do revisions of reconstruction and that if I don’t tell him – he doesn’t know.

So – he knows. I feel like the weight of the world has been lifted and am now ready to focus on fine-tuning.

Escape…to Gwinganna.

26 Apr
I’ve been dreading doing the whole ‘this time last year’ thing. I hope that in time the vivid recollections I’m currently able to make about my diagnosis (to the point of remembering the exact time, what I was wearing) will fade.
For now, I just wanted to get out of the house, away from the situation I found myself in this time 12 months ago.
An escape to a health retreat couldn’t have been more perfect if I’d deliberately set out to organise it. But I hadn’t you see.
In a lovely turn of events, I’ve been gifted a delightful weekend at Gwinganna, courtesy of a special woman who was at an event I spoke at last year.  You just never know who’s in the audience and what they might take from what you have to say. This lady who works at Gwinganna very kindly gifted me a stay at this magnificent retreat, saying ‘by  sharing your experience you will help others, I’m choosing to give something to you because I can.’ Wow……
Spectacular setting (within an hour from home), beautiful caring staff, incredible organic, healthy, nourishing food, clean fresh air, peace and quiet…a truly lovely way to take stock of how dramatically my life has changed in the past 12 months and to prepare for the next surgery.

12 Months On..

22 Apr

Today, marks a year since I sat in Dr D’s rooms and heard the term DCIS for the first time.

That’s the day my life changed forever (the significant changes to my body of course came later, another bizarre kind of anniversary to mark).

No shock, no fear, no grief, no sadness – just relief he was detailing what could be done to prevent it from progressing to the next stage and determination to get the process underway. Boy, did I feel lucky.

The sadness and at times disbelief is only just starting to seep in. What a year?!

For as long as I live I think April 23 – date of diagnosis, May 20 – date of bilateral mastectomy (plus to a lesser degree the surrounding dates on which I had the lumpectomies, partial mastectomy and later the reconstruction) will always hold a bit of a heavy, painful weight. It thankfully will be balanced by the gratefulness I feel to be here.

Thanks again, to everyone involved. Happy Anniversary.

Relay For Life 2010

21 Apr
Thousands of people, walking around a picturesque lake for 18 hours.
These teams of people had spent a year gaining sponsorships for their big event.  It began late afternoon with an official opening, then some of us pulled on a purple sash declaring ‘SURVIVOR’, with tear-filled eyes and giant smiles of relief that we are survivors, we walked…. cheers and applause from others lining the route.  Overwhelming emotions.
Team members continued the relay and as night fell, a moving candlelight ceremony.  Collectively we remembered those lost to this disease, honoured those going through treatment and hoped with all of our hearts, for a cancer free future.  This was tough for everyone, but particularly hard for Paul.  We lost his father ‘Pa’ less than six months before my diagnosis.
The efforts continued throughout the night, participants fighting aches and pains, tiredness and the rain…. I didn’t manage to go the distance, but know many who did and am so impressed.

Who Would Have Thought?

16 Apr

Certainly not me, or anyone who knows me well.

12 months ago to the day, it was just like any other day (Friday) at work. I was fulfilling my role as News Director dealing with the station’s operational requirements, then methodically assessing releases, doing interviews, editing grabs, writing content, pulling together rundowns and presenting news during the drive show (I was covering Ange’s leave in this timeslot) with Mal Lees and Luke Bradnam.

The 6pm bulletin came and went – at the end of which, Luke – with whom I’d worked since day one at Hot Tomato, casually said (whilst still on-air) “so that’s it Katie, another week?” My response was an off-the-cuff “…yeah, this is my last bulletin with you guys”. “Whadda ya mean? EVER?” Luke quizzed. “No, I’m just off for a couple of weeks, on leave”, I replied.

I was going to have those bi-lateral lumpectomies on the Monday. Surgery booked. No big deal. Just wanted the lumps out.

Despite the four months of backwards-and-forwards, different scans, mammogram, biopsies etc. I think there were two things going on at that point; I may have known deep down there was a lot more than just a fortnight’s leave in store, and perhaps – somewhere in my consciousness I did realise that yes – that may in fact have been my last bulletin.

There’s part of me that is still obviously grieving for that ‘some sort of normal’ that I was so comfortable with. I do miss being on-air – it’s a tremendous buzz and something I worked very hard at, I always tried to do well, then do better.

Today however, as I mourn that particular career (and let myself indulge in a little moment of ‘geez, it’s sad…..I really loved it’), I began a trek down another path. I did my first media interviews as the spokesperson for the Gold Coast office of Cancer Council Queensland. Here am I answering the questions rather than asking them, crafting a response in order to push a key message, rather than searching for a compelling and easy to understand statement (grab), and having a good old belly laugh at the irony!

One Door Closes….

15 Apr

You know the saying…

A lot has happened these past 6-8 weeks.

At the end of the rope when it came to trying to re-integrate into the hectic, demanding 7-day-a-week responsibility of being News Director, failing at trying to negotiate a Part-Time alternative and really struggling with the prospect of walking away from the profession I’d thrived in for more than a decade – I made the difficult decision to resign.

This brief description barely scratches the surface really – but you can imagine – it was tough. Although my departure was made slightly easier by the fact that I’d been absent from the newsroom and station for the best part of a year, going in to remove my personal items was so hard. I stood in the chaotic, noise-filled (monitors/scanners/feeds etc.), but empty space – feeling like a foreigner. Cleaning out my desk was one thing – entering the sound-proof booth, with the panel, prompter and headphones I’d used on so many thousands of occasions brought me to tears. I’d reported on and presented so many stories over the years, this is where I’d done it for the past 6-or-so and now – I was leaving. I haven’t really been that angry at the cancer (okay – sometimes when limited physically) – but here I was feeling like it was forcing me out of my chosen career. I was sad, miserable in fact – and pissed off.

Within a few weeks, I’d accepted a fabulously interesting position with Cancer Council Queensland. The application process was entirely different to anything that I’d experienced in the performance and reputation based world of radio! As Cancer Action Co-ordinator I’ll be involved in promotion of prevention and early detection messages and campaigns.

Fancy that!

And – it’s Part-Time! So that time to really get back on my feet, maintain my fitness, keep writing, continue designing and dressmaking is now mine.

There’s more to come of course, but what I really want to share is that I feel incredibly blessed to have this opportunity. The organisation is doing such worthwhile work in cancer control – trying to lessen the burden of this hideous disease (through prevention and early detection, support and professional programs), whilst conducting research which may one day lead to a cancer free world. It’s very early days I know – but this feels like a good fit – I can use my professional skills as a communicator and my personal breast cancer experience to try and make a difference. Everyone in this organisation is dedicating their work life (and then some), to that mission. Lucky huh? Who would have thought?!

Strength & Shape

2 Apr

With the help of my oh-so-funny physiotherapist Tanya – things are slowly getting back on track.

Tanya has very quickly cottoned onto the fact that I’m a determined and somewhat pig-headed kinda girl. When I’m ‘in the zone’ things at pilates go well, when I can’t shake a headache or don’t really feel like doing a particular exercise (for very good reason of course!), there’s no making me.

We share lots of laughs while navigating our way through exercises including ‘elephant’, ‘nasty tummies’ and ‘pole dancing’!

It’s actually become a bit of a family affair, with Paul joining us once a week and having survived her initial consultation – my Mum will also be coming along on a regular basis.

Another loss.

2 Apr

One of the most likeable characters I was ever to meet in the wonderful world of radio – was Mr Kenn Bacon.

When I first started doing casual shifts covering the early morning news or weekend afternoon sport at Sea FM & Gold FM, I had the pleasure of working alongside this larger-than-life, ultra-enthusiastic, mad-about-music announcer. Kenn was hosting a hugely popular show ‘Saturday Night Rock’, which was broadcast to every corner of the country on the RG Capital Network.

Kenn always backed up the following morning, eagerly assisting others in his work as a Minister.

His friendship and skills combined at the altar for Paul and I – Kenn’s booming voice, liveliness, sense of humour and serious compassion provided us with a truly unique ceremony.

I am desperately sad at learning of Kenn’s recent passing, to tonsil cancer. One of the cruelest twists to his personal battle, is that in the latter stages the disease stole his beautiful voice.

How blessed we were to have known Kenn.