Posted in Flowers, Photography

Celebration …

I finished my radio therapy treatment on Thursday last week. The final four treatments were ‘booster’ treatments, which I found quite terrifying. No goggles, no holding my breath, just a really big machine zapping a very targeted part of me at close quarters. I almost asked for the goggles back, then realised I could just shut my eyes to avoid being confronted by the bigness, closeness and scariness of the machine.

Each treatment was over quickly though and Emma would drive me home while I felt a little more shell shocked each time. I have no idea what I would’ve done without her.

It was fabulous to have Emma stay with us (Photo by Tim)

I’d somehow forgotten about, or perhaps thought I was immune to, the side-effects though. Apart, of course, from fatigue.

I can’t say I wasn’t warned. Karen, my radio oncologist, told me about the potential for them, as did the breast care nurses, and others I’ve spoken with who have gone through similar treatment. I even wrote about them on this very blog a few weeks ago, yet I was still caught off-guard.

A sunburn type response.

Redness.

Swelling.

Peeling.

Pain.

I wrote in that earlier post: ‘I might get all of these, some of them, or none.’

I got the jackpot – all of them.

The good news is that they probably won’t last more than a week or two (or maybe three or four).

And the other good news is that I’ve had company since halfway through my treatment – others to share my daily annoyances with. Probably not good news for them, but I’ve appreciated having Emma (who stayed an extra week with me) and now Deb to whinge to.

I also had the foresight to take some sick leave and I’m very pleased I did. I couldn’t have coped with going to work on top of everything.

But this is getting boring now. And if I’m bored by it all, I’m sure you are too. So I’m not going to write anymore about it.

****
On Sunday, Alison (aka Number 6) decided to spend the day with us, celebrating ‘me’ – my birthday earlier in the month and the end of my treatment.

Alison knows that I love to photograph flowers and so we went to the Queen Vic Market and bought loads: carnations, daisies, bluegum leaves, wheat that had been spray painted, and others I have no names for.

The outside table was strewn with flowers and leaves and twine and special scissors for cutting the stems and ribbon; palings from a fallen-down fence were put to good use as a backdrop and a surface; a tabletop was perched on the backs of kitchen chairs so we could shoot against the white wall under the clothes line; a shiny black tile and a sheet of black cardboard was set up in the kitchen as a different kind of photographic space … in amongst this chaotic space Alison managed to create a beautiful bouquet, and a delicious dinner.

It was a fabulous way to spend an afternoon!

Yellow daisies

 

 

These are beautiful even though I don’t know what they’re called

 

Gorgeous lilac roses

 

Spray painted wheat

 

Alison’s bouquet

These are just some of the shots I took – and if the wind stops I might take even more.

Thanks Alison! Let’s do it again some time.

Posted in Life

The final countdown …

I’ve had fifteen radiotherapy treatments so far and fatigue has hit me hard.

It’s a feeling of total energy loss and of heaviness in my body. Apparently, fatigue is one of the most common side effects of cancer and cancer treatment and can stick around for weeks and months after treatment. 

It doesn’t affect me all the time – at the moment, for instance, I have some energy (mind you, I just ate dinner) – but at other times of the day it hits and I’m left feeling empty and almost unable to move.

It’s weird though because resting doesn’t always help, so it’s not like I should quit doing exercise or should start laying around all day watching Netflix – as enticing as that sometimes sounds. In fact, that might make it worse. In the spirit of not resting too much, I walked the 1km to the local shops yesterday morning and found it very difficult to walk the 1km home. It was a very slow trip back.

Fatigue hasn’t only affected me physically. I’ve found it’s taken its toll on me emotionally and mentally as well. I’m exhausted after an hour and a half at work, I can’t concentrate on tasks that would normally be unproblematic, I’m more short-tempered than usual, and I’ve been having trouble sleeping. So much so that my GP prescribed sleeping tablets. I’m so desperate for a good night’s sleep I’m even taking them.

Fatigue isn’t the only side effect of my radiotherapy treatment but it’s certainly the one having the most impact on me at the moment.

Information the Cancer Council’s published on coping with fatigue tells me to exercise if I can, and if I’m already used to exercise, to take it easier than normal.

My GP told me on Thursday to only go to the gym if I find it enjoyable, to not push myself, and only ‘do nurturing things’ there. I made sure to tell Tom, my trainer, that that’s what my GP had said, and on Friday I had a very nurturing workout. No deadlifts, all weights reduced, and I didn’t have to go as fast on the bike or cross-trainer as usual. I have to say, I did feel better afterwards.

The Cancer Council information also advises to ‘do the things you need and want to do. If you have people around you who are able and willing, let them take on some of your usual activities’. As I have no family in Melbourne (apart from Alison), this seemed to be an impossibility. That’s not to say Tim isn’t fantastic, but I can’t rely on him for everything.

Fortunately for me, Emma, my youngest daughter, John, her husband, and Lincoln, their 3 year old son were prepared to come to Melbourne to help us out. Emma has driven around Melbourne like she’s done it all her life – driving me to work, to treatment, to the class I’m taking two nights a week in the city and wherever else I’ve needed to go. Between her and John they’ve made endless cups of tea, packed and unpacked the dishwasher countless times, vacuumed, put washing on the line and taken it in, replaced the battery in Tim’s scooter, gardened, been on bin and recycling duty: in general, been a huge support.

I have to admit to being worried about having an energetic 3 year old  around, but Lincoln has been a true delight. He’s such a sweet boy and loves stories, telling them and reading them. His new favourite is Pete the Cat, but he’s also partial to Russell the Sheep and Giraffes can’t Dance. We read stories in my bed the other evening before dinner and he fell asleep to the soothing sound of my voice.

John and Lincoln went home to Tassie yesterday, while Emma decided to stay for another week to continuing supporting me in my final week of treatment.

Yes, only one week to go and then I’m done with radiotherapy!

It’s been a confronting, challenging journey but I’m blessed to have so much support.

Let the final countdown begin!

Love spending time with this gorgeous boy!

 

Posted in Life

It’s my birthday …

… and I’ll deadlift if I want to!

Here’s me in action at the gym this morning*.

About to deadlift 40kgs

 

I reckon Tom will make this heavier next time!

I don’t usually get this visually visible on my blog, but I saw a post by my cousin Jen this morning on Facebook where she told her friends that I was ‘awesome’. It made me stop and think why someone would say that about me. Seeing yourself through someone else’s eyes can be a useful exercise and I suddenly felt proud of myself for continuing with my personal training sessions while going through radiotherapy treatment. And so I asked Tom (my personal trainer) to take a photo of me this morning because I wanted a record of this.

Plus it’s an interesting looking contraption!

Apart from being my birthday, it’s also International Women’s Day today and as I celebrate I feel blessed to have so many awesome women in my life. They continually inspire me and support me and I know my life would be less rich without them.

*****

Thanks to Tom, my trainer, for taking the photos.

Just one note Tom. Josh gave me flowers on my birthday last year. Just sayin’ …

Posted in Life

A new daily routine

Arrive. Hand over your patient card with a smile. Fine thanks, you reply to the smiling friendly receptionist who asks, somewhat unnecessarily you think, how you are. You take a seat as directed and wait for your name to be called by one of the radiotherapists.

Through the glass sliding door into the change room. Dress/top off. Bra off. Gown on. Stuff clothes into the green bag.

Carry it into the treatment room and put it on the chair. Hi. Good thanks. Name, date of birth, address.

On to the hard cold bed of the machine. Whoops, forgot to take your arms out of the gown again. Off the bed. Arms out, clutching the gown around you as you try to retain some control over exposing your body to strangers. Give that up and climb back on the cold hard bed of the machine with the gown unwrapped underneath you.

Whoops, forgot to take your glasses off. Off the bed, drop glasses into the green bag while clutching at your gown to hold it up. Back onto the bed.

Goggles on. Arms above your head and hold the bar. Legs up as they put the red cushion beneath your knees. Feeling thankful to have been doing abdominal exercises with Tom lately.

Lying there unable to see what’s going on, listening to the numbers flying between the two radiotherapists, feeling them mark your body, the cold of the tracing making you feel more exposed. Lie heavy as we move you Sharon. Left arm lifted into position, left hip shifted, ribs moved.

The cube is taped to your stomach – although you only know it’s a cube because you’ve heard them mention it. You can’t see anything because of the goggles.

The bed goes up and up – to shoulder height. You can’t see it because of the goggles but you can feel it from the way they make their final adjustments.

Sleeves of the gown are draped over your breasts.

All good Sharon. We’re out now.

A pause and you lie there watching the white square in the goggles.

A voice over the intercom. When you’re ready, a slow breath in for a short one. The yellow bar floats into the blue box and turns green. And breathe normally.

Silence.

When you’re ready, another slow breath in for a short one.

In

Hold

Great. Breathe normally.

The machine whirs and clicks like a cicada, the bed jolts into position and you see your spine and ribs on the screen in the goggles. The word pug seems to be repeated down your spine and you wonder what that’s about.

Okay Sharon. When you’re ready, a slow breath in for a long one.

The yellow bar turns green and you concentrate on keeping it there, only barely aware of the machine’s high pitched squeal.

Holding

Holding

Wondering if you can hold any longer. The green bar wobbles, bounces up and down gently within the blue box, and you clench your jaw with the effort of holding your breath.

Just when you think you can’t hold anymore, ‘And breathe normally’.

You can tell you’re struggling to bring your breathing under control by the way the yellow bar bounces around. You breathe out, all the way out, and hold. Your breath swoops into your body and the yellow bar flies up the screen. Hold. Breathe out. Just as you get your breathing under control ‘when you’re ready Sharon, a slow breath in for a long one’.

The machine whirs and spins, or at least that’s what you imagine is happening from the noises you can hear. You can’t see anything because of the goggles.

Holding

Holding

The green bar wobbles. You concentrate hard to keep it there.

Holding

You want to close your eyes but you can’t because the green bar might turn yellow. You think about how good you are at breathing. You remind yourself of your years of practice. That makes you want to laugh and the green bar wobbles and you get the giggles and it wobbles some more. You clench your jaw even tighter but some giggles escape along with some breath. Luckily the blue box is just wide enough to contain it. You tell yourself this is no time for jokes but then your other self tells you that if now isn’t a time for jokes then when is? And you argue with yourself while the machine squeals its high pitched squeal and your arms tingle from holding the bar above your head and the green bar bounces gently and ‘breathe normally Sharon’.

The screen in the goggles turns back into a white square. You lower your arms gently because they’re really hurting now and remove the goggles. I’ll take those says the radiotherapist as he comes back into the room. He lowers the bed and you sit up, lifting your legs over the red knee cushions, clutching your gown around you as you stand, stuffing your arms into the sleeves and covering your body to counteract the feeling of exposure. A too-late gesture that nevertheless makes you feel somewhat in control.

You put your glasses back on, pick up your bag, yes see you tomorrow and smile as you head to the change room. You rub MooGoo udder cream into your left breast, dress, unlock the change room door, push the green button to open the sliding glass door, wave at the receptionist, go through one more glass sliding door into the hospital corridor, turn left and make your way to the car for the 32 minute drive to work in peak hour traffic.

Another one down. Only eleven to go.

Yellow … this time unconnected from my breath
Posted in Learning, Life, Schools, Teaching

An inspiration

I was already a grandmother by the time I started teaching at university in 2000. Phil, who turned 20 earlier this week, and his brother Scott were my only grandchildren till Ronan arrived in the world eight years after Phil. Then Jordan and Hunter and Sakye – and then more and more and more!

As my list of grandchildren grew I started to think more and more about the student teachers I was teaching and I’d often say to them ‘You never know, one day you might be teaching one of my grandchildren – they’re scattered all over Australia – and that might mean me popping into your classroom to have a chat and see what the grandkids are up to’.

Perhaps unsurprisingly, it’s come to pass. Some of my grandchildren have had the pleasure of being taught by some of the very special people I taught at university and it’s always lovely to wander into their classrooms and see them as teachers now, after seeing them as students. I don’t pretend to have any influence on who they are as teachers, but it’s lovely to see them nonetheless.

I’ve been teaching for over 20 years now. Being a teacher was something I never imagined I’d do. Debbie, my sister, had always wanted to be a teacher, but it hadn’t been on my list of career choices.

I no longer teach those preparing to be teachers in primary and high schools; rather I find myself running workshops for academic staff who are teaching university students studying for degrees in commerce and accounting and information systems and business analytics. While I know nothing about accounting and commerce and business analytics I do know something about teaching.

And, what’s more, after running six workshops in the last week I’ve been reminded that I love it. I love teaching. I love asking questions that generate thinking, I love putting ideas out there and seeing how others develop them, or consider them, or debate them, or draw insight from them.

Those who know me in person, know that I’m not a dynamic person in ordinary life, but I seem to get another sort of energy when I’m teaching and as I get older and therefore more comfortable and confident with my teaching persona I find I turn into a warm and funny and energised person who is enthusiastic and passionate and insightful.

Well, at least that’s what I’ve been told.

I’ve had a few positives in terms of my teaching and supporting teachers over the last twelve months. I (successfully) supported a team of academics in their application for a VC’s award for outstanding contributions to student learning, and on the back of that award the team was encouraged to apply for a national award.

We found out earlier in the week that we’d been successful at the national level and so, as part of a team, I now have an AAUT (Australian Award for University Teaching) citation for outstanding contributions to student learning under my belt. They only awarded 60 across the country this year, so I’m pretty chuffed with that.

Last year I was successful in applying to become a Senior Fellow of the (UK) Higher Education Academy. Being a Senior Fellow means I ‘demonstrate a thorough understanding of effective approaches to teaching and learning support as a key contribution to high quality student learning [and] impact and influence on other colleagues through, for example, responsibility for leading, managing or organising programmes, subjects and/or disciplinary areas’ (www.heaacademy.ac.uk).

It was a 6,000 word application supported by two referee statements (thanks Robyn and Sharon B) and required a lot of evidence to support my claims.

The awards are great – even though they require a lot of work and the collection of a lot of evidence from over my 20 years of teaching and are a great recognition of the work I’ve done.

But much (much) more meaningful than the awards and fellowship came in the form of a text message from one of my daughters-in-law last week.

It turns out that Jada, one of my granddaughters, is being taught this year by someone I taught at university. Here are the messages I received:

Met with Scott [teacher] for a parent-teacher meeting this evening. He may have lit up like a Christmas tree when Jada mentioned your name (we had to go through the “Do you know Grandma Sharon” *blank look* “my grandma Sharon Pittaway” dance before he twigged).

He said you were his all time favourite lecturer and that you allowed students to give their own perspective on things and that you never just read or regurgitated information from a textbook. He said this made you inspiring. He also asked for me to pass on his regards.

He ALSO said that Jada no longer needs to come to school as she is now an A+ student because she knows ‘Grandma Sharon’.

I’m glad he took the no school rule back-Jada would have run with that!
I made Scott out as being kind of excited, he was more yelling “oh my god” and “really??” He was flailing his arms around a little and slapping his thighs haha. Congratulations to you on making such an impact on people and allowing them to filter their enthusiasm for learning and growing through to the next generation. I’m especially grateful they are our kids!

He said the way I taught made me inspiring.

That’s worth more (much much more) than a VC’s award or a national citation or a senior fellowship.

That’s real!

Jada, reading … because teachers are amazing!