It’s 3am, I must be lonely…

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..

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.

Nursing Conference – me!

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..

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..

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.

Mother’s Day 2010

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.

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.

12 Months On..

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

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?

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!