Thursday, October 29, 2009
I'm PUBLISHED!!
I am sooooo excited. I am officially "published". YAY! A massive thank you to Jess for making the article happen. Kinda ironic that October is Breast Cancer Awareness month.
What's next? World Domination.. one newspaper article at a time. Mwoahhahahaaaa Mwohahahahahaa!
Here's a copy of the article I wrote:
“The Perspective Bat”
I call the day I was given my cancer diagnosis, the day I was hit with “The Perspective Bat”. Being 32 years old didn’t make the news any easier. I honestly thought Breast Cancer only applied to women over 40. That it would never happen to me. Well, the battle I’ve fought and subsequently won over the last 9 months has taught me a scary but valuable lesson. Cancer doesn’t discriminate. It doesn’t care if you are a good person, a mother, a child, a teacher or a lawyer. It doesn’t care what you do, if you donate to charity or rescue orphaned animals. It can affect all of us, so we must be smart and diligent, doing everything we can to keep this disease at bay.
Cancer doesn’t have to be a death sentence anymore. In fact I prefer to think of it as a ‘Life Sentence’. The journey becomes an opportunity to reflect, re-shape, re-connect and re-evaluate. I certainly wished many times over the last year that I had worked out a little more (and perhaps consumed a little less wine) but at the end of the day listening to your body and getting checked are the most important things we can do. Early detection saves lives, it’s a simple fact. I know, because it saved mine.
Despite being scared, questioning why, and the occasional moments of despair, so much good has come out of my battle this year. Facing mortality at a young age has enabled me to make necessary changes to my life, to ensure the rest of it is a good and long one.
Chemotherapy makes you re-evaluate things you once considered important. I liked having long hair, it made me feel.. well… like me! Once it was gone, I became a naked version of myself. But like a phoenix rising through the ashes, I feel reborn with my new hair, albeit it a little fuzzier version of itself. Vanity became redundant once I saw myself looking like the Dalai Lama. It just wasn’t important anymore. Friends, family, unconditional support and lots of laughter, these are the important things that truly get us through life’s adversities.
October is Breast Cancer Awareness month and is poignant to me for several reasons. Firstly because it’s the month where the disease, that could have taken my life, is brought to the forefront of all of our minds. It’s the month I came home to my incredibly supportive and wonderful friends, here in Wanaka. It’s the month I was told I am officially in remission and the month of my birthday, that I will celebrate with more fervour than ever before.. but with a little less wine… maybe….
Thursday, October 15, 2009
Toto, I don't think we're in Kansas anymore....
Home Sweet Home! I can't believe I left here on the 16th of February, crying, scared and here I am... 15th October (Happy Birthday Ian Reiser - kisses!!) home again, in remission and with a newer healthier outlook on life. I am absolutely over the moon to finally write EMMA - 1, CANCER - NIL. Takes more than cancer to keep this bitch down, heh heh.
We got into town on Friday, it was freezing cold. It was snowing at ground level at Lake Tekapo and the mountains were all covered in snow, but you wouldn't know it today, sunny, balmy and blue skies.
Friday night, the crew all got together in front of the fireplace at Woodys (my favourite spot in the world really) and we got it on. I can proudly say there was only a few tears, we were all in too good spirits - pun absolutely intended.
The night kicked on as did the drinks. For those of you not on Facebook, I ended up playing pool and drinking with Shaun White (no.1 snowboarder in the world) with my mates. I had no idea who he was and decided in my alcoholically-induced wisdom to call him my "bitch" as we downed shots at the bar.
It wasn't until I googled him the next day that I began to groan and slap my head. How was I to know the man is a snowboard / skateboarding god, Olympic gold medalist, worth millions with a lamborghini and his own playstation games on the way? Not that it would have mattered mind you.
Well, at least he will probably remember me now ("remember me? I'm that drunk cow in Wanaka who kept calling you my bitch"). Anyhoo, many drinks later I appreciate Craig throwing me into a cab and sending me home, sometime around 3am... thanks guys!
Melbourne was wonderful to me in so many ways. I was able to get the best treatment, perhaps in the world. I re-connected with my amazing family and I got to spend time with my beautiful friends, Leon, Liss, Ian, Claire, Max, Chrissie, Ash, Glen Husko, Toomer, Bianca Wilson, Jo Bo, Steve & Catriona, Morag, Renee Marais, Steve & Caroline, Clare (from NZ) and heaps others....... but I have to say that finally, I really do feel like I am home.
Virginia, Jet Boat James, Ruthie 1 and Ruthie 2 and everyone who went out of their way to help, from flowers in the house, to cleaning our cars (who does that???) THANK YOU from my whole family. We have never felt so loved and appreciated. I am so blessed to have you all.
I sit here, having just come back from a walk down the road. The sun was shining, the ipod was cranking and the mountains were breathtaking. I took a moment, turned my face to the sun and just breathed.
When was the last time you did that?
Love you guys
xox
Friday, October 2, 2009
PLEASE READ THIS
You can’t spend five minutes in a room with me, tell me that I look good considering and get any idea of what I have been through in the last year. I want to tell people that, despite my smiles I've been tested emotionally, physically and poked, prodded and pulled every way possible. I have been left a shell of my former self.
The fact that I smile makes the journey seem easier to those in my life and I am glad that I exude that, but those people never spent an hour every day on a steel table undergoing radiation therapy, which left me blistered, broken, sore and tired in a way I never thought was humanly possible.
They weren’t there on the days when my family and I wondered if this disease was going to kill me.
They weren’t there for the surgery, when I was told I'd lose my nipple or my breast and that I still might if the cancer comes back. That I will never know what it is like to breast-feed a child.
They weren’t there on the day when I was told I was unique, because I was young. Because I was single. Because I had never had children. That mammograms or testing for genetic breast cancers wouldn’t apply to me. That I was a medical anomaly.
They never stared in the mirror at my patchy pathetic looking head as the hair fell out in clumps.
They weren’t there on the days during chemo, when I didn’t have the strength to walk to the bathroom or the state of mind to take my own medication.
They weren’t there on the nights I cried myself to sleep because the twilight felt a million times more lonely when you’re away from your friends, your job and you had forgotten where you belonged in the world.
They never puked into a bucket with me, watching the anguish in my sisters eyes as she stared helplessly, wanting this to end and to have her sister back, the way she was.
They never sat there with the fertility specialist who told me if I lose my fertility, that adopting an overseas child was a good option as Australian law practically precludes me from selection for adoption with a history of having cancer.
They never saw me cry after hanging up skype from Mum and Dad or Craig or Kate, who told me they loved me and meant it in a more sincere way than I had ever heard before.
They never heard from Mark, who told me for the first time in 20 years that he had no idea how to be there for me right now.
They never knew I wondered why I was deserving of any admiration for just trying to get through this.
They never understood the notion of being surrounded by a hundred people and yet feeling totally alone. Waking in a lonely, single bed, with no man beside me to tell me everything was going to be all right.
I don’t tell you this in hope of sympathy… only that you may get some insight. That some people project an image of strength, but deal with internal adversity every day. I may smile on the outside but that doesn’t mean I don’t have moments of pure despair too.
I met a woman while going though radiotherapy. I was in the waiting area, sitting like I did every day, in my blue hospital gown with a smile on my face, rubbing my bald head, trying to think of something funny to tell the radiotherapy team to help make the day go quicker for us all. A sweet older Italian woman sat beside me. She told me her name is Paula. She asks me where my cancer is and I tell her I have breast cancer. I go on about the indignity of having to get my boobs out everyday for the invariably changing (and often male) radiologists, thinking this will at least get a chuckle out of my fellow cancer patient.
She smiles and tells me that I’m lucky. She has rectal cancer. She says the only thing worse than the actual cancer is the loss of her dignity having to show her ass to the world for the last 6 months and knowing it is all in vain. She tells me with a brave and heartfelt smile on her face that she is losing her battle. I become acutely aware that this is the last time I will see this lovely lady. I muster all my strength to maintain my smile for her and not shed a tear. I am suddenly feeling like the luckiest person in the room.
Take a moment, dear reader, and put yourself in my position. I am a single 32 year old woman with breast cancer, who meets a women with terminal rectal cancer and considers herself lucky?? Please just take a moment.
I sit here on a Friday, aware that the rest of my friends are drinking, laughing and screwing their ways through life tonight - for which I am eternally grateful. I however, find myself trying to accept this lesson from Paula and all the other amazing people (their faces flash through my mind as I write this) I have met over the last 8 months that will lose their fight with this awful disease. Each one of them, someone’s mother, father, brother, sister, wife or husband has amazed me with their will to live and to accept their fate with their heads held high.
I hope beyond everything, that my story provides YOU with some strength throughout your own battles to stay on this planet even just for one more day, because god knows some beautiful people I've met are fighting for that chance.
Please also know this. That regardless of what hand life deals you, that I will be there with open arms, to hear you, to understand you and be there for you unconditionally. Because if nothing else, my beautiful friend, of all my useless questioning why, I was given this challenge to enable me to be there for those I love, as you, have been there for me.
Sound simple? Perhaps it is.
xxx
Tuesday, September 29, 2009
Eye of the Tiger, Pan-flutes, hernias and hysteria....
The music was one of those cheesy Asian imitations of Chariots of Fire. As soon as the badly synthesized string section kicked in mixed with a Casiotone styled Bossa Nova drum beat, I couldn’t help myself. I started smiling… then my smile turned into a chuckle… and as the music became more and more dramatic (boom boom chuckka chukka – da da da da daaaaa daaaaaa, boom boom chukka chukka) I ended up just losing it in a fit of giggles.
My poor masseuse didn’t know what was going on. He must have thought he was tickling me and that was why I was laughing, so he started massaging my lower back even harder, which was getting painful, but I was laughing so hard by this stage, I couldn’t tell him.
By now, the song has hit full crescendo (since when did Chariots of Fire have bird noises and a synthesized guitar solo??). It started to sound like the London Symphony Orchestra had all had a hit on a crack pipe and were in the room with us, playing stoned. Meanwhile my little Chinese man is about to bust a hernia using all his strength to pound the crap out of this chick on his table, inexplicably laughing her ass off. Picturing the scenario made me even more hysterical. The poor guy didn’t know what to do so kept going, harder and harder. I was soon a beaten, broken mess on the table, choking red and unable to breath, tears streaming down my face, into the hole in the table and forming a pool underneath me. Finally the song finished and I was able to draw breath.
The masseuse stopped the torture and excused himself sweating and breathing heavily, to get a drink of water. I was thinking to myself how this was the best $20 and 20 minutes of the funniest shit ever as I wiped the tears from my eyes. Finally with my hysterical fit well and truly over, I relaxed back down and my exhausted but undefeated masseuse came back into the room to start on my neck…
Then the next song started… Eye of the Tiger with pan-flutes… oh dear god…
Friday, September 4, 2009
Never washing my head again!!!!
All I can say is wow. Last night, not only did I go to an absolutely kick ass concert by Ben Folds, but I got to meet and hang out with the guy. I will try to get all of this down, because I still have to pinch myself that it all really happened!
Two days before the concert, my sis contacted the Palais Theatre about a possible 'meet & greet' with Ben. Not holding out much hope, the day of the concert arrived with no response from Sammys emails. At 2pm, I had resigned myself to not meeting the man and got ready for the concert. I was just so excited about seeing him live.
Dad rang at 3pm saying he had just spoke to Sam and she still had not heard from anyone, so a little disappointed but still exited I jumped in the shower and got ready. Unable to accept defeat Dad made a phone call to Frontier Touring to see if there was anything they could do. Dad rang me back about 5 minutes later and asked if I had some nice eye make-up?? When I asked him why… he said "Because you are going to meet Ben Folds tonight". I lost my fucking mind! We were going to be taken back-stage after the concert and Ben wanted to meet me. I screamed and then cried ... lots.
After the a mind-blowingly great concert with just Ben, a grand piano and two hours of incredible music, the lights went up and dad got a call from Gerard and down to the lobby we went. Gerard was a lovely guy with a big smile who shook our hands, gave us both back stage passes and off we went, back through the theatre, through the stage doors to the back of the stage full of roadies and sound gear. Dodging cables and low doorways we made our way through a maze of corridors into a waiting empty dressing room.
The whole way there I was telling Gerard how nervous I was, but he insisted it was unnecessary as Ben was such a good guy and that they were happy to be able to be able to do this for me. He offered us both a water and returned with a couple of bottles for us while we waited for Ben to arrive. We didn’t wait long. Ben walked in, cool as a cucumber with a beer in his hand. He walked straight up to me and gave me a big hug. I couldn’t believe it!! I said it was such an honour to meet him. Ben said it was cool and he was pleased to be there as he shook Dad's hand. He was totally relaxed and really happy to be talking to us. I was surprised that the 4 of us were the only people in the room. He was totally there for us!
We talked about how awesome the concert was. He thanked us but said he'd made some stuff ups. He'd just come from doing two nights at the Sydney Opera House using a Steinway grand piano, which he had liked and gotten used to. He felt all out of whack when he played the piano here, which explains why he was mucking around with the piano stool during his concert. He made a comment like “something's wrong with my stool” and the audience laughed at the 'poo' reference. I told him you couldn’t tell that he had made any errors and that the crowd was really interactive and just loved him regardless. Then I said “besides, it gives you an opportunity to say fuck". He laughed, then realising my dad was ok with the swearing, he said he “fucked up” a couple of times, which was cool.
I asked if he was classically trained, as his piano performance blew us away. He said he plays by ear (after mentioning his musical start was in bass guitar and drums – he didn’t even sit at a piano till he was 23). He said he hears the melody in his head and he bangs it out on the piano until the tune sounds the way it does in his head, which was fascinating. He is such a prodigy.
Dad thanked Ben and said how much this meant to me after the rough year I had so far. I noticed that he was looking at me when Dad was saying that and I was looking down and I agreed that this was the best thing that had happened to me this year. He said he was more than happy and then mentioned that I looked great considering (he said on two separate occasions how good I look which was so sweet).
Ben talked about his father-in-law going through chemo and I said that my hair was growing back with a vengeance. I took off my head scarf to show him. He said “Ooh, can I touch it?” and I was like “Sure go for it!” and I bent my head in his direction and he RUBBED MY HEAD!! "It's so soft!" he said, which made us all laugh. It was so weird hanging with the guy, like he was an old mate!
I told him he is always welcome to come and stay with us if he ever heads over to Wanaka and he said he'd love to (imagine the sing along around the piano!). Then this guy Shannon from Fontier Touring said he wanted to get a couple of photos, so Ben put his arm around me and I did the same and we had two photos taken. I was beaming, as you can see!!
We talked about heaps of stuff, from his wife Fleur getting her helicopter license, to his passion for photography. He was so chatty and amiable and kept smiling at me. Finally, Ben said he’d like to see me again soon or something like that and I said, "Problem is I won’t be sick then, I’ll be all better!". He just laughed and said “that’s cool make up some shit and come see me backstage again” and gave me another big hug. Ben was incredibly humble and really didn’t seem in a hurry to leave at all, considering he had just done a gruelling 2 hour solo performance. He was totally calm, funny, kind, warm, smelt great and was affectionate and reassuring.
Thanks to Sammy, Dad, Gerard and Shannon at Frontier Touring and of course, thanks to Ben. You have made this girl very, very happy. This is one of the best things that has ever happened to me and means so much considering the shitty year I've had so far. I am so blessed. Thank you, thank you, thank you.
Wednesday, September 2, 2009
So excited!
Dad loved ‘Whatever and Ever, Amen’ so much he used to take it to work with him (the coolest Dad) so I knew he’d be stoked I bought him a ticket too. Besides… it’s nice to be able to do something with Dad that doesn’t involve hospitals and cancer stuff for once.
Ben Folds and I seem to have been crossing paths for many years now, but finally I am in the right place at the right time to see him, kinda ironic considering the year I have had!!
I had a small epiphany yesterday when I was raving to the folks about the brilliance that is Mr Folds. I realised that I have been listening to him for nearly 15 years! (age denial is a wonderful thing). His music has been a real constant in my life though not always at the forefront… more like a background theme, like the ‘musical score’ to the film of my life so far. The man is a genius. If any of you haven’t heard of him, you are missing out. If you love amazing jazz/rock styled piano, stunning harmonies (ELO & Supertramp would be impressed) catchy and gorgeous melodies and some of the sweetest most profound lyrics of our generation, ch-ch-check him out.
You may know him from the song Brick which was a bit of a commercial hit years ago (“She’s a brick and I’m drowning slowly”). Also his rendition of “Bitches Aint Shit” is frigging hilarious! So do yourself the favour.
Anyway, I digress …
Radiotherapy is racing through now. I am officially in Week 6 as of tomorrow and I can't wait to finish. The side effects are really kicking in now and I just want this phase over so I can concentrate on the next phase... Hormone Therapy.
Sadly, we need to shut down my reproductive system over the next 5 years, as my cancer cells are attracted to the estrogen in my body. At absolute worst I may need to have a hysterectemy.. at best I will be rendered chemically menopausal (yes, with all the shitty symptoms of menopause) for 5 years. Not fun at all as we just don't know if we will be able to re-start my system when all of this is done. The thought of not being able to have children weighs heavily on my mind. This is just not cool stuff for a single 32 year old to have. Sigh!
I am so over all of this to be honest. I am sick of it all. I am sick of hospitals. I am sick of worrying. I am sick of.... well... being sick. I just want my life back!!
On a happier note, I am generally in good spirits. My hair is growing back with a vengeance and it's a glorious sunny day in Melbourne.
Gonna run now, love to you all as always. Thanks so much for the continued love and support. You are truly the wind beneath my wings (bleck!)
xxxx
p.s Ben’s a wicked photographer too. Check out some of his photos on Twitter… especially the ones where he has used infra-red film. They are amazing.
p.p.s I have to report that CHRISTIAN SLATER is following ME on Twitter! I don't think he really knew what he was doing.. he had about 400 fans following him on there and he went through and clicked to 'follow' all of us! So he is getting updated every time I post a tweet. Hilarious!
Thursday, August 20, 2009
I'm still alive...
Hey Guys
I am blogging to you from Balwyn which is somewhere between Box Hill (where I get radiation therapy) and my new home in Ivanhoe. I am sitting here with mum and dad and I got dad to agree to a photo (despite his rotten flu) so everyone say HI to Dad!
Yep, I am officially in my own place and I LOVES IT!! I'm staying in hospital run flats with lots of old ladies who drink tea in the common room, but the peace and quiet absolutely rocks. I awoke to the sound of birds chirping from my balcony and the sun was streaming through the kitchen window and I finally realised I am in Week 4 of radiotherapy. FUCK YEAH!!! Only a couple more weeks to go and I am done.
Had a bit of a drama this week, whilst staying at my cousin's house, their dog decided to break into my room and chew my only pair of very expensive glasses. I was devastated. Anyhoo, I went to the Optometrist and he said he would do a new eye test to check my prescription. Whilst looking into my right eye he said unfortunately my optic nerve was swollen. At worst, that could mean a metasticised brain tumour. I had extensive MRI tests done yesterday and I am thankful to say that after a couple of sleepless nights, I am in the clear. I don't have a brain tumour *Arnold Schwarzenegger voice "It's not a tooomer"*
So feeling on top of the world right now. On the count down to getting home - for me, that's Wanaka. I miss everyone there soooooo much.
Best go, before this coffee rush wears off.
Love you all.
Ems xxx
Wednesday, August 12, 2009
Radiotherapy... what a blast!
Hey guys
Sorry again for a bit of a delay in posting, so much has happened over the last month including moving house, changing hospitals, commencing radiotherapy blah, blah, blah that I just don't have the energy to recount it all right now. I've just come back from a lovely dinner followed by cake and coffee with Mum, Dad, Sam and Gareth at a gorgeous little restaurant in Fitzroy and I'm a little food-sleepy. But otherwise I am fine.
I'm so excited to be back online after an enforced hiatus. Moved to be closer to treatment in Box Hill which meant I have been living in the 'burbs with no internet access, no mobile phone reception and no mode of transport. Has been so tough. I may as well have been in bloody outer Mongolia! Damn, Melbourne is a big, big place!
If only I could have got my hands on a flux capacitor.. it all would have been fine, but alas there doesn't appear to be any DeLorians (or plutonium for that matter) in the area. So until a time machine lands miraculously in my driveway (or until I find alternative accommodation) I am a little unaccessable at the moment. You'll have to bear with me, but hopefully it will only be for a short time.
Funnily though, not being able to access the internet for over a week has caused quite a stir, unbeknownst to me. All my overseas cyber friends were worried and even assumed I was dead!!! Some of them only know I am sick and have cancer. They didn't know my prognosis, so when they never heard back from me they assumed the worst ha ha. When I finally Twittered my existence tonight, they all replied back how relieved they were that I was still alive. Good thing I didn't have condolences and cards sent to my parents eh!
Just goes to show how internet dependent I have become over the last 6 months. Usually I would consider that a little bit sad, but considering the internet has been my lifeline and best method of communication over the year, its a dependency I am happy to have. Also without it.. I wouldn't be able to bore the crap out of you guys for 15 minutes or so each month that I post crap like this heh heh.
So, I am officially now in Week 3 of radiotherapy. I am being treated at the other Peter Mac hospital in Box Hill as they had a much shorter waiting list (told ya, radiotherapy is all the rage in 2009). The staff there are incredible and I continue to be amazed at the kindness and support offered to the patients. Its still humbling.
Radiotherapy itself is a total walk in the park compared to Chemo. The biggest hurdle is getting to the hospital every day for treatment. I was having to catch two trains from the house I've been staying in, which was taking me over an hour each way. That sucked ass. But Dad bought a nice Honda and decided he wants to drive me to treatment from now on, as the fatigue starts to kick in... so I am being driven to the hospital now which is wonderful.
Well, my cup of tea is getting cold and I have another episode of Top Gear to get through. I was recently indoctrinated into the series by my cousin and I am well and truly addicted. Also have decided after watching Jeremy Clarkson drive the Bugatti Veron from France to London, that is the car I want. It does 400kms an hour with 1,000 brake horse power and costs around 1 million pounds (see above picture)... but I still want one. Hot, hot, hot.
Ooh speaking of hot... there's a stunning fair haired Italian guy who works in Joe's Garage restaurant on Brunswick Street, Fitzroy. If you ever go there, tell him Emma says HI ;)
Hope to be heading back to Wanaka in October and I am getting so excited. I miss everyone so much and I can't wait for the catch up. I'll be having a week-long party at my place, so everyone needs to get into 'training'. I just wish I could pick up my friends from all over the world and have everyone there with me, at the same time. You have ALL been so wonderful. I feel so totally blessed. I can honestly feel the love all the way over here, so thank you for that.
Ali and Mike... guys I am so completely disappointed that I can't be in London in September for the wedding. Ali, you're my oldest friend and I almost can't bear the thought of not being there for your special day. Please just know that I am there in spirit and sending you all my love and best wishes. I am staying focused on making it up to you when I get to the UK next year, happy and healthy. Love to the whole family and bloody good work on 'Animal Cops - Arizona'. I saw your name on the end credits and was very excited! It's a wonderful series and I'm so proud of you both!
Love to you all. Sleep well. Sweet dreams.
Ems xxx
Wednesday, July 15, 2009
Monday, July 13, 2009
Introducing my bald head! No you can't touch it.... oh... ok then... it is kinda fuzzy and soft....
Hey guys,
Sorry for not posting sooner. There is no excuse, but I am quite good at making up bullshit on the spot should some be required ;) Well, I recently made an incredible discovery, whilst in the kitchen making myself a cup of tea Sammy said - all very concerned "Em you have a rash on the back of your neck" and she started to poke and prod. "We'll have to mention that to your oncologist when we next see her" (Sammy is the doting and concerned sister you WISH you had. I love it!!).
So when we next saw Dr Grossi, Sam pointed out the rash which actually turned out to be a rather large Port Wine Stain birth mark, which I never knew I had under all that hair. So in true hard-core blogger style, I took a photo and posted it on the internet for all the world to see.
Everyone... meet Birth Mark.... Birth Mark... meet everyone :)
Well, Mum and Dad finally made it to Melbourne and were rudely introduced into the wonderful world of chemo in their first week here. They were amazing, coming into the hospital with me and sitting there for the four hours it takes to make me sick for a month. They took good care of me during the week, cleaning out my bucket, bringing me food/water/medications and just reassuring me it would all be over soon. Thank god they were right.... I HAVE OFFICIALLY FINISHED CHEMO PEOPLE!! Thank god for that! Please cancer, never come back.. I just don't think I could ever go through that again.
Um what else, oh yeah... Radiotherapy. So I had to go into the hospital again (can do that trip blindfolded now) for my radiotherapy 'measure up'. I had to lay on a CT scanner table, half naked, breasts exposed and very cold while 6 people fussed around me and drew all over my top half. They use all the lines and dots to line up the 'lasers' on the machines so they can specifically target the cancer areas. OK here's the weird bit, they tattooed me! Yep, you heard me right. I now have 6 blue dots tattooed on my chest, two down the middle of my sternum, two down my right side next to the breast and two on the left. My doctor said they can either spend 40 minutes drawing all over me every day for 6 weeks to line up the machine each time, or they can just do tattoos with a needle and some ink. Needless to say I opted for the tattoos. I prefer lying there cold and exposed for 25 minutes as opposed to an hour... what can I say, I am not much of an exhibitionist! Mind you, if I had those fake boobs that pointed upright while I lay down, it might have been a different story ;)
Ahh cancer... it continues to be a source of shits and giggles doesn't it? Unfortunately, there is a waiting list for radiotherapy, so I am biding my time for the next couple of weeks. Can't wait to get started. Sooner I start, sooner I finish. Then overseas here I come! Wow, tattoos, bald head.. all I need now is a Harley Davidson and my transformation into a scary biker chick is complete!
On the upside, I bought 2 tickets to see Ben Folds on 3rd September in St Kilda. Ben is a piano/musical genius and I am such a huge fan. It's lovely to have something like that to look forward to. Ladysmith Black Mambazo are also playing at the end of the month, but I blew all my pennies on Ben. Argh Melbourne, so much good music, so little funds.
On the downside I still haven't heard from Josh Groban. I thought Jamie's tireless efforts emailing the poor man on Facebook would have surely resulted in him declaring his undying love for me. I think he is just playing hard to get. That's ok Josh, I too can play hardball... there's still plenty of time for me to stalk... ahem.... I mean talk to you ;)
Saw 'Kung Fu Hustle' over the weekend. What a great movie! Ah Leon, you continue to be a source of never-ending fun. You are the wind beneath my wings? nah... sunshine in an otherwise cloudy day? nah... you are the peanut butter on my toast. Yep. You are the camel-coloured, crunchy nut spread that brings joy to my tummy. Thanks for being my peanut butter, my incredible mate.
Ems xx
Friday, June 12, 2009
'Cause when the wind takes you, it takes me, too
You look at me, with uncertainty,
You look at me, with urgency.
You look at me. with fear in your eyes
like you're about to fall away.
But don't be afraid to change your colours now.
I've known you all Summer, you rose above it all.
I see you hesitate to fall now,
But it's a pretty good view from down here, too.
And when the wind takes you, it takes me, too.
When you change colours, I change mine, too.
Try not to think, and I will try too.
When you let go, I will let go, too.
I knew you when you were green and strong.
You were like a feather on a wing, so long.
You know I will miss you when you are gone,
but don't be afraid if you just can't hang on.
'Cause when the wind takes you, it takes me, too.
When you change colours, I change mine, too.
Try not to think and I will try, too.
And when you let go, I will let go, too.
The cold air is pushing hard on you.
I know what you're saying; I can feel it, too.
You'll go through changes, and I'll go through them too.
Don't be afraid now, no don't be afraid.
'Cause when the wind takes you, it takes me, too.
When you change colours, I change mine, too.
Try not to think and I will try, too.
And when you let go, I will let go, too
The lyrics kinda make me think about this journey I'm on and the fact that you, my amazing, incredible friends are on it with me. All the way. I have never felt so completely blessed,as I do now. Strange... I know, but I am so honoured to have you all in my life. I just wanted to tell you that. I don't think we tell each other enough. So there it is. A simple but important message to you.
Love and peace
Ems xxx
Wednesday, June 10, 2009
Feeling like a human specimen in the petrie dish of life...
*thanks to Megan for the pig-picture above, laughed so hard I nearly spit my tea out*
NOTE TO SELF - don't make jokes about Swine Flu, then get sick in Melbourne "Swine Flu Capital of the World". Chemo = immuno suppressed/compromised = easy bloody target.
Result of irreverent and somewhat unfunny jokes about contracting Swine Flu? Being admitted to hospital with suspected Swine Flu:
1. Spending 4 days in quarantined isolation in hospital
2. Having a whole ward on red alert
3. Only being touched with latex gloves, full body aprons and even then, only when absolutely necessary
4. Blood tests, blood tests, blood tests and then some blood tests (this is only the first hour of Day 1)
5. Not being able to even leave your room for 4 days
6. See #5, therefore having to use a bedpan (oh the shame)
7. Having your veins physically collapse, resulting in blood being taken FROM YOUR BONY FEET by someone from ICU (after trying my wrists, hands, arms) man that hurts!
8. Being told you have the blood pressure of a corpse
9. Having a temperature of 39.7 degrees and feeling like your face is about to peel off
Finally I am home, safe in the knowledge I did not have Swine Flu, but just a serious viral infection (er.... yay!?)
Still feeling dazed and confused, stuck with more needles than a Kings Cross junkie who just won lotto and like I just wondered off the set of "Outbreak".
Sigh... I just don't want to talk about it anymore.
Saturday, June 6, 2009
I got sick last week. They think it was swine flu, I told them my nose has always looked like that
So people, its Friday night. I have had a shit of a week (can't wait to regale you with it) but what's your excuse for hanging out in my blog on a Friday night? Get your butt off the chair, turn off your computer and get out there!!! For godsakes people, if not for yourselves... DO IT FOR THOSE WHO CAN'T!! Get drunk, get stupid (and most definitely get laid).
Ahhh... all better.. had to let that out. Now on with the irreverent babble that constitutes this fine blog of mine :)
How the hell are ya???
I had chemo again on Monday (yeah yeah Em, we know it "sucked ass" get on with it) ahem - hate it when the voices interrupt me.... where was I?? - oh yeah, I ended up in hospital the next day on a drip severely dehydrated and worse for wear. It would appear my bucket won this round, but hey there's always next time to look forward to. Yep, sad but true, my oncologist confirmed I have to have another round of chemo on 22nd June. Damn! For some reason both Sammy and I had convinced ourselves that this would be the last one before I start radiotherapy. Oh well, send back the clowns, the bouncy castle, the vodka sprinklers and the monkeys on unicycles (at least for now).... but I'm keeping the cabana boys ;)
I managed to get a bit sick last week in Canberra visiting relatives (they think it was swine flu, I told them my nose has always looked like that) so that is possibly what tipped me over the edge this week. I really felt like dying... but hey, you know me, I always stay positive... and the good thing about feeling like you are dying? you can only go UP from there lol.
Exciting news, my ma and pa are coming over to Melbs next weekend. Really looking forward to seeing them. It feels like I have been in a time warp and my head spins to think I have been here since middle of February already. Wow time flies when you're having fun eh!
So what else... I am starting to worry I have spread myself a little thin. With Facebook, Hotmail, the blog, Twitter (shudder), the books, my work with Oceana and eventual world domination, I fear I may have bitten off more than I can chew. I only agreed to do the Twitter thing so I could stalk... ahem... 'follow' Josh Groban... but I am finding it strangely addictive. But did I really need another opportunity to vent witty Emma anecdotes * into cyber space?? Not sure really. I'll keep you posted.
*(N.B "Witty Emma anecdotes" was a term loosely used for comedic purposes only. No assumptions of hilarity or general frivolity on the part of the author should ever be made and no comedians were hurt in the making of this statement)
Speaking of posted, I have been a little remiss with this blog... my baby, but people, people, people.... you have been bad, bad followers also! Where are all your comments? I wasn't kidding when I said I wanted bloodshed, tears and wars on these pages (see first post). Ok, I'm going to count to 10 and when I start.......
1, 2, 3, 4, 5.......
Friday, June 5, 2009
Thursday, May 21, 2009
"Life is what happens while you're busy making other plans" John Lennon
Sorry for the delay in posting. As you may or may not know, I had my second round of Chemo last Monday 11th and I have to report that this time was worse than last time. We think it may be because my reserves were already depleted from the first round, but Round 2 seriously put me on my ass (literally). I've been totally bed ridden for the best part of a week and got well acquainted with my bucket. Again, the chemo brain is the strangest part. Leon came over last week for, what we now call 'Risotto Tuesday' (man that boy can cook!) and as I told him on the phone last night, I really have no recollection of him coming over. Poor guy... I promise your company does not suck Leon!
It's my evil mind ticking over here, but maybe I could use this to my advantage! I could pretty much do whatever I wanted and a couple of days later... poof.. it's gone from my memory... so I am open to your equally evil suggestions. We could get up to some serious mischief!!
So that being said, the next round on June 1st will probably be worse still. BUT the good news is that I am over the halfway mark now. So everyone give me a big FUCK YEAH!!!
I am such a night owl. It's 1.10am and as usual I am wide, wide awake. If only I could get paid surfing You Tube videos, hanging out in cyber space, listening to music and writing macabre short stories.... I would be one rich lady right now, that's for sure!
Have caught up with still more cool friends and more have already booked their tickets to Melbs. I would love to think they are all coming just for me, but it does help that I am based in the arts capital of Australia (not to mention the food, booze, nightlife etc) .... so methinks that may also have a part to play in it ;)
What else... oh yeah, Simon Clark got engaged. Congratulations honey! Let me know some more about your wedding plans and I will do what I can to get on a plane to be there.
Nick and Vick Wilkinson (two of my favourite people in the world) had a gorgeous baby. Brodie is an incredibly lucky boy, he's got two fricken awesome parents. I am so happy for you both!
Also excited that Mum and Dad will be heading over here around mid June. I can't believe I have been here three months already! Hopefully they will be staying for a couple of months, which is going to be awesome.
Man, I love Melbourne, but I seriously miss Wanaka. I google earth it all the time. Miss the mountains, my friends and sitting by the fire at Woodys. Dad's been telling me about all the snow they are getting. Sounds like I am gonna miss a bumper ski season.... argh! Bollocks. Balls. Hmph.
Anyhoo, onwards and upwards. Gonna head off now and polish my very very bald head. Why, you ask?? Just because I can.
Love you all
Ems xxx
Sunday, May 10, 2009
The Perspective Bat
Had an awesome day. I caught up with a friend and we went to the Richmond Hill Cafe in Melbourne, which has an in-house fromargerie (cheese shop). We gorged on lovely teas and a cheese platter with all the trimmings. I was in cheese heaven!
I must admit the only thing that would have perfected the afternoon is a glass of crisp white wine to wash down all that lactose, but since I was diagnosed I haven't wanted to drink any alcohol at all. It's strange - my friends can't believe it, I am rarely without a beer or wine in my hand lol - but I just don't want to put anything bad into my body at a time like this. So I am being extremely well behaved.
Can't wait to start getting my travel plans into action. Travel (and apparently now.. cheese) are my focus. I spend most nights roaming the planet, thanks to Google Earth. Went from Bordeaux to Budapest to Malibu, CA last night.... not bad for a nights work eh.
Back to the fun stuff...
My hair continues to fall out at an alarming rate and to be honest, they never prepare you for how bloody messy it is! It doesn't all fall out in one neat heap on the floor, it falls out on your pillow, in your clothes, in the shower... all over the fricken place. Its messy and its annoying and yes, I am embarrassed to admit, I still cried like a little girl when it first started to come out in clumps.
My apologies go out to any friends who went prematurely bald. I am sorry I never took the time to ask how you felt about it, so please accept my very belated hugs.
It's very upsetting to see yourself looking like you wondered out of a concentration camp. Even though I had mentally prepared myself, to some degree, it was and continues to be a shock as each day goes by. I stare at myself in the mirror, wondering who that person is staring back at me. Is all of this really happening???
I wonder about a lot of things now. I call cancer "being hit with a perspective bat". I think about the journey of learning to like myself again after all of this.....
So, dear reader, how are you doing? Thanks for checking out my blog and for all the emails you continue to send. It really lifts my spirits :)
Hope you have a wonderful Mothers Day. Don't forget to tell your family how much you love them. If that's not an option, for whatever reason, do something wonderful for yourself. I highly recommend a gourmet cheese platter.
I am about to waste a ridiculous amount of time on the couch watching Monty Python movies.... sigh.... bliss!
Love to you all
Ems xx
p.s still hoping by some small miracle that Josh Groban will call me for a date... will have to find out if he likes cheese or not. If not.. I may have to rethink my celebrity crush ;)
Friday, May 1, 2009
Back from the brink....... geez I feel like a drink!
Well, I am back from the dead.... only just. Wow Chemo is as bad as everyone says/thinks it is. There is no sugarcoating it. It is a bastard!. I had my first treatment last Monday and was bed-ridden and sick for the best part of 5-6 days. Well, at least I know what I am in for the next couple of cycles. But everyday since then, I am getting better and stronger. I was able to walk around by about day 3-4 and stopped feeling like I wanted to throw up and pass out at the same time around day 4-5.
Am slowly feeling more like myself each day, which to be honest feels amazing. Just to feel 'normal' again feels like a blessing and I am starting to get a more normal colour in my face. Was a nice shade of grey for the best part of the week.
The "chemo brain" they mentioned is the strangest part. My mind is a jumbled mess some days. I watched a movie two days after the chemo and then had absolutely NO recollection that I had seen it. I would have sworn black and blue that I had never seen it, until Gareth (my brother in law) mentioned that I thought Ashton Kutchers hair had looked shite in it (sounds like me lol). All of a sudden that triggered a memory and although I still cannot remember a thing about the film, I became aware that I had indeed seen it. I can only compare it to getting really really drunk and having no idea what you did the night before, until someone mentions a keyword and some of it magically comes back... anyhoo you probably know what I am talking about and if not... that's ok, I can put this rambling down to the "chemo" brain.
Been having some seriously scary nightmares and 'night sweats' which can be a part of it too and had my first ever migraine (due to the anti-nausea medication I am on). Wow that sucked ass! I feel so sorry for anyone who has migraines on a regular basis. I felt like someone had stuck a shovel in my head! Thank god I woke up today and it had gone.
So anyway, apart from all of that, I am doing fine. I didn't really want to post all the negative medical stuff, but thought that some of you might find it interesting from a symptamological (is that even a word?? If not... it should be) point of view.
In the interim, I am doing well. I am charging through the Hard stage of Guitar Hero 3 and listening to lots of great music.
My current songlist top 15 is:
Love Always Remains – MGMT
Human – The Killers
The District Sleeps Alone Tonight – The Postal Service
Cherry Blossom Girl – Air
Soothe Your Pain – Dub FX (saw him busking live in St Kilda)
In Our Gun – Gomez
Butterflies and Hurricanes – Muse
Kashmir – Led Zeppelin
Can’t Run But – Paul Simon
You Don’t Know Me – Ben Folds
Shape of My Heart – Sting
Grapefruit Moon – Tom Waits
Seven Nation Army – The White Stripes
I’ve Seen All Good People – Yes
If you haven't heard any of the above songs, let it be your task for the week. Trust me, you will thank me for the experience!! If you email me at emschranz@hotmail.com I can send you the mp3s.
OK, I love you guys!
xx Ems
Tuesday, April 28, 2009
PLEASE HELP!!
The Peter MacCallum Cancer Hospital and its amazing staff has saved my life and made this horrible, horrible time just that little bit easier. Everyone from my Surgeon and Oncologists to the Breast Nurses, administrators and even the Volunteers (cancer survivors, who gave me scarves for my head and hold our hands and rub our backs during chemo) have been incredible. The support, warmth and professionalism of everyone there has simply been mind blowing.
Please help us to give something back and to ensure that if this terrible disease afflicts someone in your life, that they will have the incredible support and treatment that I have.
Peter MacCallum Hospital may be in Melbourne, Australia, but the research they do to find a cure for cancer... reaches everyone on this planet.......
http://runmelbourne.everydayhero.com.au/samantha_glasgowschranz
Saturday, April 25, 2009
Monday, April 20, 2009
Chemo Day 1
So I will fill you in on Chemo - Day 1...
After a visit with my lovely Medical Oncologist, Sam and I headed up to Level 5 to the Chemo ward. I was gutted to discover I had just missed Drew Barrymore on the Ellen show. Drew is the one woman I would totally turn gay for....
Anyhoo, the nurses were lovely and did their best to calm my nerves, however, I have to admit to you all that I failed miserably. I sat in my big chair and proceeded to bawl my eyes out. They had to partition me off from the other patients as I didn't want to upset them and I couldn't stop the tears so that was that really.
After the wonderful sedative kicked in, I started to feel much better and only had some mild hallunicanations of men on rooftops (don't ask me why) before I felt like I was ready to deal with this. Sammy had a hold of my hand the whole time, and whilst she was trying her best to reassure me and be strong for me, her eyes told a different story. I can honestly say that I think today was as tough on my beautiful sister and brother in law, as it was on me. Even though the drugs were being pumped into my veins, Sam was experiencing everything I was going through. All I can say is that is one hell of a connection there. We have always joked that we felt more like twins than sisters. She is my rock, my support, my surrogate mum and my best friend. I am so blessed to have her in my life.
Ok, here's the details. Firstly, they pumped a bag of anti-nausea drugs into me. That took about 15 mins. After that was the "Adriamycin" (also known as Doxorubicin). This is the evil shit. The stuff is red and the nurse needs to stand with her hand on me the whole time it is being pumped in as if it hits the skin it burns the tissue like acid (wow and that shit is going into my veins?). This is the stuff that can cause Leukaemia - albeit very rarely. This is also the stuff that makes hair fall out and it is mainly used to treat breast cancers. I hated looking at that red liquid going down the tube and into my arm. I thought about pinching if off just before it had to go in, but I think she would have seen me do it.. and it would have made the chemo a bit redundant eh! Scary to think that to save my life I have to pump poisons into my body, but I guess its the lesser of two evils. Cancer is just full of wonderful ironies!
After the Adriamycin goes in the Cyclophosphamide goes in (hence why my chemo is called "AC"). This bag takes about an hour and is covered in black plastic (may as well had a skull and crossbones on it and a big POISON sign on it... looked ominous enough!). In all, we were there for over three hours.
I have left with a bag full of drugs and have my bucket beside my bed. Apparently everyone's symptoms are different, so I am keeping it close just in case. Hey... even if I don't spew, but my head falls off in the night, at least it will fall into the bucket and that means less mess for everybody.
I have a feeling I may not be able to stand up in the morning, based on the fact that I can barely stand right now. All in all, I am still pretty numb. I have a shaved head and did my first chemo.. I am entitled to feel like I have been hit with a mack truck I guess.
So goodnight my beautiful friends... here's to sweet dreams, 6ft tall dark handsome men and .... heads not falling off in the night.
I love you all
Fuck the lump
Ems XXX
Friday, April 17, 2009
Short and sweet
Well, here it is folks. Me with really, really short hair. Victoria Beckham I am not! I must admit, it is very liberating not having any hair. I get out the shower, run the towel over it and I am done! Should have done this years ago lol.
Don't have a whole lot of fodder for this blog entry. Saving it for this weekend and the BIG SHAVE on Sunday. Leon and his clippers have a date with my head.... lets just hope its not shaped like a half-sucked lemon. Just got home from the hospital and the volunteers have given me a whole stack of funky head scarves and beanies for next week. I especially like my USA stars, stripes and glitter one and the Pirates of the Caribbean red one with skull and cross bones. Don't worry there will be plenty more photos to come.
Big thanks to Leon and Alyssa for the "Fuck the Lump" hoodie and t-shirts. You guys already do so much! I wear the hoodie all the time now... am scarily resembling ET at the moment. Wanted to thank Anna Kemp for sending me a card from the other side of the world and to Bianca and Mark for taking the time out of their Borneo holiday to send me a postcard... do I get to keep the Orang-Utan who delivered it? He's super cute and actually better looking than the last guy I dated!!
Hope to be catching up with Russell tonight (my old tennis doubles partner). We haven't seen each other in a long time and he is a beautiful soul. He's one of the best writers I know and leads a fascinating life in the middle east and all over the world. Looking forward to making him dazzle me with his Capeoria... Cappoeira... Kapo.... fuck it... Brazillian Martial Arts skills.
Other than that, been hitting the Melbourne Comedy Festival shows and DOMINATING in Guitar Hero. I am up to the Hard level now and looking forward to next week's showdown with Max Leong (from Applecross). Gonna make him eat my Guitar dust!!!............. erm..... that doesn't even make sense Em!?!
CONGRATS to Saskia and Craig on your engagement guys. I am soooo happy for you both. You are such a gorgeous couple and we can all aspire to be in love as much as you two are. Wish I could be there with you to smother you in kisses and cuddles.
Love to you all, more this weekend.
Peace
Ems xxxxx
Tuesday, April 7, 2009
Waiting.... waiting....
So ...... I am cooling my heels and it sucks. My chemo is due to start on the 20th April. We need to wait until all the surgery stuff heals before we can begin due to the risk of infection. Whilst I am not in a hurry to have the chemo and all the horrible side effects, I kinda want to get this show on the road so I can get on with the rest of my life... so as it stands I am just waiting.
Sadly, I wasn't in a position to get any eggs frozen. Not enough time. But I am confident if kids are in my future, that it will happen. I am leaving it in the lap of the gods and just hope I end up with a wonderful understanding man..... sigh..... do they even exist??
I am filling my days with writing (the book is coming along nicely), reading books and marvelling at the stupidity (and cuteness) of Sam's cat. It's like living with Rain Man. He's my best friend and surrogate boyfriend at the moment.... without the benefits of course..... sickos!!
Sounding like a broken record here, but I am constantly feeling compelled to say thanks to everyone for being so awesome and keeping my spirits up. Every day I am getting letters, cards, emails, facebook pokes and all sorts. It's always a little ray of sunshine when I head down to the letterbox and find things addressed to me that aren't from the hospital, so THANKS SO MUCH!!
Got a joke for y'all....
An Englishman, an Irishman and a Scotsman all walk into a bar. The Englishman turns around and says "what a fucking cliche!" mwhahaaaa mwhwhaaaaa.
Ok pimps and geezers, I am off. Sending my love to you all and thanks heaps for tuning into my blog. I would love some more comments being posted on here so I know I am not just talking to myself in cyber space... because... well.. that would just be lame.
Take care and speak soon.
Love Ems xxxx
Friday, April 3, 2009
Wednesday, April 1, 2009
me so artistic...... autistic..... confused....
A shout out to my amazing friend Bianca, who just sent me a card and CD of pics and videos from Sound Relief at the MCG 12th March (album is on my facebook page) ..... YOU ROCK DUDE!
Monday, March 30, 2009
Breast Cancer? Breast Schmancer!
Out of 1,000 women; 125 will be disgnosed with breast cancer. Of those 125 women, 8 will be under 40 years old.
See.... I am special!!!
I have an appointment with a Fertility Specialist at the Womens Hospital Monday, but we don't know if we have time to harvest / freeze any eggs (even though I want this very badly) prior to commencing Chemo, so I will probably just have to buy a baby on ebay.
After the chemo I will be having Radiotherapy, then 5 years of Hormone treatment. The cancer is most likely to try to return within the first 2-3 years, but we'll talk about that stuff later.
Sorry guys, I got nothing tonight. This has been exhausting today and I just don't have it in me to even try to be funny. Thought the picture above was fricken hilarious though... so that will have to suffice for today.
Thanks so much to Steve and Catriona for the "music" gift card... you know me so well. I will be downloading some tunes tonight. Thanks for the beautiful thoughts and words. Massive love and appreciation from me to you.
I will try to post again this week, as I actually had a wonderful surprise over the weekend and a great weekend to boot (funny photos included) and I absolutely must put them up here, just don't have the energy right now.
Miss you and love you all.
Ems xxx
Thursday, March 26, 2009
Monday, March 23, 2009
Updates on non-cancer related stuff
Saturday, March 21, 2009
Out of Surgery
Thursday, March 19, 2009
Thanks for coming and welcome to my blog.
I figured this was a pretty cool way to keep in touch with y'all, so I hope to log in daily with written blogs and video posts (depending on my mood). Please leave me comments, start fights, write poems... whatever floats your boat.
This blog is for you guys as much as it is for me and... oh... I don't know... do whatever the hell you want to!!
I hope you can all share this experience with me and laugh lots and cry occasionally too (I know I will cry when I have to shave my head - big girls blouse) *sings "It's my Party and I'll Cry if I want to" *
This is a safe space people. I want your jokes, your frustrations, your questions, your thoughts, your smiling faces and most importantly..... your SOULS!!! Mwhahaaaaaaa Mwahahaaaahaha.
So anyway, welcome to F*CK THE LUMP.
Peace Out