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Wednesday, September 28, 2016

Clowning around

I was asked to be a parent speaker at a conference for The Humour Foundation last week. If you don't know what they do, go to the website and have a look, but THF is responsible for the wonderful work done by the Clown Doctors and Elder Clowns. I was asked to be a parent speaker because Clown Doctors have been a part of our lives since they first careened into the Royal Children's Hospital many moons ago.

I had such a lovely time at their conference. What a wonderful bunch of people! I felt so welcomed, so at home and so grateful for the wonderful bunch of human beings that bring so much joy.

My speech made the clowns cry....and they gave me a standing ovation. I broke the clowns, people!

After my speech they made me an honorary clown!



And then we had a raucous game of Bogan Bingo. Folks, you have not played bingo until you've played Bogan Bingo with a bunch of clowns!

The following is the transcript of my speech.

Hi everyone and thank you for having me. Yes, I am Leisa and I am Mum to four now adult children – Sarah is 29, Chloe is 26, Tim is 25 and Riley is 20.
At first when I was asked by Jo to come and speak I didn’t really know what I was going to tell you. I have no words of wisdom to impart and know nothing about clowning other than the fact that my children can tend to get highly embarrassed with my antics down at the local shopping centre – groovy dancing in the aisles, lip synching to the music they play over the PA and having conversations with automatic tellers.
So….I’ll tell you what your impact has been on our story.

The Royal Children’s Hospital has been a part of my life, our lives, for as long as I can remember. I went there as a baby, when I was six and again when I was 14. I was fortunate not to experience any complications in regards to my condition so my own visits to the hospital were few and far between, however my memories of being there are seared into my brain – and not necessarily in a good way. Appointments and treatments didn’t seem as child focussed or holistic – and of course back then there were no such thing as Clown Doctors who I am SURE would have made my visit a whole lot more memorable in a GOOD way! In the 1970’s the focus seemed to be on the clinical side – diagnosis and symptoms and wanting to know if I was reaching all the expected milestones rather than who I was as a person.
I’m glad I didn’t go there too often.

Most of my dealings with the Royal Children’s Hospital were as an adult – as a mother. Our first visit was a prenatal visit in 1986 and then became regular occurrences after the birth of our first daughter back in 1987.

We never expected that the Children’s Hospital would become such a big part of our lives. As you can see, I was born with a form of dwarfism – the most common form known as achondroplasia. My husband at the time was also born with dwarfism – a different type to mine. Both of us enjoyed relatively healthy childhoods with very little or no medical or surgical intervention. When we decided to have children we had no reason to expect that our children would not have the same experience.
It didn’t work out that way.

The Royal Children’s Hospital became a big part of our lives for almost thirty years. In the early years of raising our children, every few months we would spend an entire day at the Children’s as we’d have multiple appointments at several clinics. You name it, we’ve been there – ultrasound, x-ray, MRI, medical photography, neurology, neurosurgery, bone dysplasia, genetics, spinal and scoliosis clinic, respiratory, urology, encopresis, physiotherapy, Day Surgery, the Operating Theatres, Recovery, Inpatients, Outpatients and the dungeon – which is what Sarah used to call the room where they’d make her spinal brace.

We used to know the old hospital like the backs of our hands and I used to joke that we’d been almost everywhere except Intensive Care.

It wasn’t such a joke when we ended up there too after a frantic dash to Emergency one morning.

In the early days of our life at the hospital we learned the waiting game, and that appointment times were only guidelines. Your appointment may have been scheduled for 9am but if you were seen before 11 it was a good day. Back then PAGERS for parents weren’t even something considered. You get a PAGER now if you get tired of waiting and want to wander off and play in the playground or go and look at the meerkats! LUXURY!!!!

No, back then it was sit and wait – and over the years we learned to prepare for a day at the hospital. We armed ourselves with snacks, drinks, books, art supplies, toys, activities and changes of clothes. It was like packing for a weekend away! We learned to wait – and I guess that’s why they call us patients – because you learn to be PATIENT and wait your turn. Over the years I would people watch and learned how to pick a NEWBIE from a mile off. After 15 – 20 minutes waiting they’ll get up and enquire at the desk, mentioning the time of their appointment and the length of time they’d been waiting. I’d chuckle to myself and say, “There’s a new one. Sit down love. They’ll get to you…eventually…”

I don’t know when we first encountered the Clown Doctors doing the rounds. I know I had a few kids by then though and was a well-seasoned and tired hospital parent.
There were a group of irreverent clowns careening down the corridors towards the lifts – making noise and merriment, commenting about silly things, making jokes with children, parents and staff alike and bringing with them an element of fun. They stopped and talked with us and I specifically remember Dr. Peg who was blowing bubbles and eating them as they floated down, telling the children that they tasted like strawberries. She then became distracted and started rummaging about in her coat pockets. She pulled out a sample bottle, containing yellow liquid.

“Mmmm….!” She said……”Urine sample!”

And proceeded to drink the lot in one gulp!

Hospital visits, for me at least, became a lot more fun.

When I was preparing to speak today I decided to do some research and ask my children for some of their memories of the Clown Doctors – after all, the children are who you’re there for, right? It’s a CHILDREN’S HOSPITAL so the focus is on children, I would assume.

Each of them told me that they remember the Clown Doctors being there, they remember talking and laughing with them….but they were so overwhelmed with everything that was happening to them that they found it difficult to focus and fully engage with them. Their thoughts and worries were focussed on their wonderings about what was happening to them and listening out for the one word they dreaded the most – SURGERY.

But please don’t think your antics were in vain. They weren’t. Please don’t think your spending time with is was wasted. It wasn’t. You helped enormously.

You helped me – their mother. And I wanted to let you know how important that was and is – helping the WHOLE family, not just being there for the kids – for although the actual procedure or surgery or condition is happening to the child and the focus should naturally be on them, the situation is affecting the WHOLE family.

And a Mum needs to be there for her child – and the other children too if there’s more than one. Yet sometimes – often in my case – she becomes so overwhelmed with the enormity of what’s going on that the relief of the Clown Doctors coming on and easing some of that tension…..well……it’s invaluable….and so healing…..even for the mother.

Honestly, after interacting with you, engaging in your silliness and sharing a laugh I felt a little more relaxed and ready to continue supporting my child.

So, I wanted to say Thank You.

Thank You for being there.

Thank you for bringing your brand of silliness that helped so much in lessening the tension.

Thank you for prescribing a truckload of chocolates for a four year old girl who was waiting to have both her legs surgically broken and reset with pins and screws and a wicked looking frame that we learned to manage.

Thank you for helping me learn that to cope with the trauma of the whole thing we needed huge doses of fun and silliness along with the midazolam, the diazepam and all those other drugs ending with PAM.

Thank you for listening for heartbeats in foreheads, and elbows and knees and big toes.
Thank you for trying to climb IV poles, running away with wheelchairs and looking at charts and telling kids that they had the biggest and smartest looking brains you’d ever seen.

Thank you for coming to see us after we had just endured the scariest and most horrible times in Emergency – where we went right to the edge and came back again, where people worked intensely and quickly, where I heard words I didn’t want to hear, saw things I didn’t want to see and was possibly more confused and terrified than I’d ever been my entire life/
Thank you for your gentle and beautiful brand of humour after we transferred out of ICU and back onto the ward. Your presence was so calming and reassuring. You broke the tension. You brought back smiles and giggles. It was your presence that assured this mother that things were OK – that the terrible night we had endured was over and we were back on the road to recovery. All you had to do was be silly. You blew raspberries on the windows, you knocked things over you juggled random things and then you flattened your faces against the window, making my girl smile the most beautiful smile in the world.

Your presence at the hospital is such an integral and important part of hospital life. You bring life and fun and silliness to a place where sometimes people can get lost in uncertainty and fear. You calm nerves, bring distraction, dissolve tension and help us all to remember that life is good and silliness and laughter is a vital part of getting better and healing.

All my kids are not kids anymore and they have graduated from the clinics at the Royal Children’s Hospital and attend adult clinics at the Royal Melbourne and Monash. They’re all responsible for their own medical care now and they do it on their own. This Mama has had to learn how to relinquish that “control”.

However I did accompany one of my daughters to her visit to the Spinal Clinic as an adult at the Royal Melbourne. It felt as though we were at square one – starting all over again. The building was unfamiliar, we were unsure of where we were going, the corridors were darker and the walls were plain and missing all the bright, happy art work we had been accustomed to for so long. We felt nervous and small.

And one of us commented……

“You know what this place needs? Clown Doctors. I’d feel so much better if Clown Doctors were here!”

And it was in that moment that I realised how important you guys are. You really are.
So thank you.

From the bottom of my heart, thank you for being there.

Monday, September 19, 2016

My darling girl.

Maya earlier this year.....at our most favorite place in the world.
27/10/2007 - 14/09/2016 
My darling girl
My darling girl
You're all that matters
In this wicked world
All that matters
All that matters 
My darling (girl)
My darling (girl)
All of my sunshine
And all of my joy
You're all that matters
All that matters.

Well I can't stop the pain
When it calls
I'm a man
And I can't stop the rain
When it falls my darling 
Who can?

My darling girl
My darling girl
You're all that matters
In this wicked world
All that matters
All that matters. 
My darling friend
My darling friend
All we've got going
Is love in the end
All that matters
All that matters.

Lyrics by Mark Knopfler.

Last Wednesday - September 14 - I held my Maya and sang to her as she crossed the Rainbow Bridge. 

I told her how much I loved her. I told her to go and find Lucy and run on the beach. I told her that I'd go to the beach and feel her with me.

I held her as that thundering heart stilled and she was filled with peace and my own heart broke and shattered into a billion pieces. 

I wrapped her up and took her to my sisters place and buried her near the dam, under some trees and camellia bushes that were blooming in beautiful pink shades. I placed a stone at her head. My beautiful nephew will be making her a better marker soon....

My darling girl found her way into my heart when I first met her in November 2007. She chose me. She plonked herself on my knee that day and kind of said, "You're my Mum. I know you'll love me just as I am." She knew I needed her as much as she needed me. 

And on the day she left she let me know it was time to let her go, as hard as that decision was to make. 

I will miss her forever....my little shadow.....

My darling girl...


Tuesday, July 26, 2016

When it comes from within

I've been thinking about this post for a week. I've written it several times in my head. It will possibly come out on the screen nothing like I planned in my head...but that's ok. Maybe this is the right telling.

Last week someone called me the M-word. In itself I guess that's no biggie. I mean, it happens. I get annoyed, I move on.

But this one came from within the "disability club" and it was deliberate. This person knew my name - my actual name. This person looked me in the eye as I did something kind and said, "Thank you little midget....oh, I mean, Leisa."

I arked right up. I didn't yell, or scream or get obnoxious, but I felt the hackles rise and I told him that there was no way I was going to stand for it. It was rude, mean and the same as calling someone the n-word. He said it was a slip of the tongue. I told him it wasn't. He knew what he was saying.

After the incident I pondered for a while. Would people have thought I should've been a little more lenient because of the type of disability the name-caller had?

My answer is no. I respect my new friend as a person, a fellow human being. I expect the same courtesies from him as I do the rest of the human race. Just because my friend has a particular disability doesn't give him an excuse to be rude because, "He might not know what he's saying." He knew exactly what he was saying and he needs to know it's not on in the same way everyone else needs to know it's not on.

I don't believe in rules for us and rules for them.

I have to admit that I was hurt. I thought they would have known better. He too would have been subject to obnoxious words used to describe his condition over the years. Back in my day people with his condition were called all sorts of things that were "acceptable" back then but are totally inappropriate now.

Back in the day the M-word was once the moniker they assigned to people like me. Not anymore. I won't take it from anyone.

Monday, July 18, 2016

These are a few (one) of my favorite things

Make way for the swans!
Image source
When I drive in to work my favorite part of the drive is around Lakeside Drive in Albert Park. Drivers have to be alert when making their way around that lake as there is a large population of Black Swans, as well as many other water birds.

(It's one of the big reasons I am so anti-Grand Prix!)

The speed limit around the lake is 50kmph and I'm pleased to report that most Melburnians seem to keep to that limit - and for good reason too. The swans get right of way in traffic - and by the way they stroll across the road you have every reason to believe that they know they own the place. They take their sweet time just waddling across, stopping to check out the scenery or perhaps wondering if they really do want to cross the road after all. Meanwhile, traffic banks up as they make up their minds and make their way across.

For some reason, I don't mind just sitting there and waiting for the swans. I don't even care if I'm terribly late for work. The swans are a bright spot in my day and serve to remind me that there are more important things to care about in this fast world.

Monday, July 11, 2016

Knitwise, Cookwise

Hi people,

Winter has settled in here well and truly. With apologies to my friends in the Northern Hemisphere who I know experience a much colder winter than we do down here, it has been cold. Average daily temperatures seem to be around 12c (53.6F) which I know isn't really cold but when you're used to summers of over 100F it IS cold!

I have been spending a lot of time knitting. I've found an easy beanie pattern and just set those knitting needles a clackin'! The good thing is that people have seen my creations and want to buy them! I have orders!

These are the beanies I am sending off to people in the post today.

Rainbow, Koorie Flag and purple flecks. 
Knitting has been so therapeutic. There's just something about the rhythmic movement that is so soothing. Knowing that I am making things for people I know and love is even better. A whole lotta love goes into what I create and I hope those who receive my creations feel it too.

I'm making a little bit of money on the side too. Just a little. Actually......only enough to pay for more wool. I don't charge for my time. I'd make a terrible entrepreneur! I look at lovely quilts and knits at markets and see how expensive they are and know darn well that they are worth every cent! I know a lot of money and time and effort goes into hand making something, but to put those prices on my items....I just can't do it!

Maybe I need to just say to people, "Pay what you can afford" like they do at Lentil as Anything.

I have also been trying new recipes and made this the other evening.

Rice and Bean Stuffed Capsicums.
I got the recipe from Sammie over at The Annoyed Thyroid, Recipe can be found HERE. It really was delicious.....actually this recipe made me enough meals for four nights so I'm set for dinners for a while! I may even add in a little chilli powder next time....and yes, there will be a next time!

Go over and give Sammie some love. She's a pretty awesome lady who loves running and Disneyland - just like me!

Speaking of running (how was that segue?!), thanks to tax time bonuses and end of financial year sales I bought myself some new running shoes on the weekend!

Bit brighter than I'm used to!
I hadn't changed my running shoes for.....oh goodness.....over two years. This is a no-no apparently when you're a runner. My other ASICS were really in need of replacing - even sporting holes where my big toes are. I could feel that they weren't cushioning or supporting my feet as I was running so it was well and truly time for new ones. I took these out for the first time yesterday morning and they felt terrific.

I'm once again on the look out for another place to live. Although I completely LOVE where I am living and feel sad about moving I have decided I need to find a place closer to family and work. The two hour plus commute four days a week is exhausting - not to mention the extra travel I have to do for dance rehearsals on the weekend. Having said all that though, I am in no great rush and have decided that I will employ the "keep turning over rocks till you find the treasure" approach to house hunting. In other words, I will look for and apply for places, however if I am unsuccessful then that place wasn't meant for me and I'll just stay put and keep on looking until the one that's meant for me comes. No point getting anxious about it! I looked through a really LOVELY little place on Saturday that I would dearly love but when I turned up I was one amongst a crowd of maybe thirty other people wanting to find a rental in the areas as well. Rental properties in the area I'm looking in are in great demand.

At least I have a place to hang my hat now. I realise how blessed I am every day when I commute to the city and see the homeless people near the train station. I cannot comprehend not having anywhere to go.


Wednesday, June 29, 2016

Hide and seek


There seems to be such a focus on the concept of finding yourself.

How do you find yourself when you never got to discover who you were in the first place?

What if your whole identity was shaped by being something, fulfilling a role through which you defined yourself - daughter, girlfriend, mother, wife?

How do you find yourself when the only "you" you knew was the one that was shaped by those roles?

I was good at those roles...well...at least I thought I was.

"Be good and do what you're told."
"Keep them happy."
"Keep them fed and happy. Love them. Keep them alive. Listen to them"
"Keep him happy."

What happens when slowly, bit by bit, those roles are no longer required, needed....or even wanted; and you find that bit by bit, day by day, a little more of who you thought you were is eroded until there's absolutely nothing left and you're left standing with empty hands and sometimes an empty head that echoes with the question, "What now?"

Go out and find yourself.

But who am I looking for? What's she like? Will I like her? I hope I will!

Who is she now that there's nothing left and she has to start again from scratch?

So....she starts. In the silence of her empty house she starts. Well...she did start with an empty house and slowly started to fill it with pre-loved things that she makes her own.

She creates things with her hands, filling the empty rooms with beautiful, colourful things that are an expression of who she is.

She eats when she wants and as little or as much as she likes.

She watches movie after move, episode after episode one after the other just because she can and there's no one there to question it.

Her sewing machine lives permanently on the kitchen table. It's on no one's way but hers. Pins, scissors, fabric and cotton litter the room at times, evidence of the creative process. Her heart burns with excitement of creating without the constraints of time. Her knitting needles are always on the go, especially during the winter months, as she creates scarves and hats for those she loves. Thoughts of selling her creations flit through her mind from time to time...

She shares of herself when she wants to share and remains silent when she can't - until she goes to her safe place where she can finally let it all out story by story until the telling is done. She doubts if the telling will ever be done. In that safe place there are no judgments or recriminations; just an ear that listens, one that doesn't care what she says. She can say what she needs to say in that room and no one cares....well....there is care but it's care with a purpose, not the care of involvement.

She wonders if she is finding herself or if she is simply just ridding herself of all the baggage she has expected herself to carry while she was fulfilling all those roles. She realises that it doesn't matter. She gets the feeling that once the baggage is gone she can truly begin.

A beginning can start at any time, she discovers - even when you've lived over half your life already.

She hasn't quite found herself as yet. In fact, she doesn't even think she's close. She is content to be on the journey.  Who knows? Maybe she will find herself right at the very end.

Tuesday, June 14, 2016

Happy Place

Morning at Lake Hamilton
 Sometimes the world simply gets too big. 

I'm not going to comment much about recent world events. I have deliberately stayed away from news and current affairs programs. Actually, I do that a lot - most days really. Watching the news unfold in front of me in screaming technicolour doesn't do my heart, mind and soul any good, not to mention the fact that I don't think news reports are entirely accurate most of the time anyway. There's always a myriad of perspectives and I know not all of them are represented in a single news report. 

You may call me an ostrich with my head in the sand. 


That's ok. I'll let you. I'm not offended. I know what works for me and I know that my anxiety levels go through the roof if I dwell on events over which I have no control. I don't think we were meant to know everything but humankind seems to have this insatiable quest to know all there is to know about everything there is to know. 

Try as I may though, news filters through. Let's face it, if you're on Facebook (Did I just make a pun then? Let's FACE it.....FACEbook.......never mind.....) you get news as it's happening so yes, I have heard about the recent tragic events in Orlando and yes, I am aware that billions of people around the globe have aired their opinions about the availability of guns, gun control and the like. 

When things like this happen I find I immediately start creating something beautiful. I guess there's something about the predictability of a beginning, middle and an end that has a beautiful outcome that I find soothing. When 9/11 happened I slowly and systematically started on a Friendship Quilt that became a wall hanging. It kept me calm and gave me another focus rather than dwelling on the horror that I had witnessed live on my television screen.

This time, without even thinking I found myself cutting out 2.5" fabric blocks from the the endless stash of off-cuts and Fat Quarters that I have in boxes in my spare room. So far I have cut out 180 of these little beauties. 


There are 11 piles of 12 squares pictured. I could've sworn I'd cut out 144 squares.......
I found the 12th pile on the floor. 
I lay them all out on the living room rug and decided that I'd do 15 rows of 12 to make it a decent sized little quilt. Laying them on the living room rug was possibly a foolish move because.....well....I have a 10 week old puppy......
Who isn't ALWAYS blissfully asleep on her little sofa!
Tonight I'm going to decide on the placement of colours - which will quite possibly be very haphazard but I like haphazard things. I'll try and post some pictures as the quilt progresses,

Centering in is my happy place. My little home, my kids, my fur-kids and my love for creating beautiful things is sometimes the only world I need to think about. Like I said, I don't think we were meant to know everything. I don't think it's good for me to know everything. I'm doing what I can to listen to my own body, heart and soul to discover the path that is right for me.