Showing posts with label cancer. Show all posts
Showing posts with label cancer. Show all posts

Friday, May 8, 2015

anchored

It's been a while since I last posted. I've slowly been recovering my strength and energy and finding out who Stacy really is after this last eventful year. There's a funny thing that happens at the end of your treatment - you expect to be relieved... you expect to be excited about the future... instead the impact of what's happened over the last year hits you hard (like a cement truck)! I've spent the last year just getting on with everything I had to do... diagnosis, surgery, surgery, chemo, chemo, chemo, chicken pox, neutropenic fevers, cancelled chemo, long time feeling awful, radiation, radiation, radiation, radiation, hormone therapy... and now at the end of it all the impact of everything that has happened, that I've been through, has hit. It's a time for reflection, grief, celebration, apprehension and excitement. Now it's all over I'm facing joining the real world. That's a bit scary. I haven't engaged with the real world for such a long time!!

When I first wrote about this journey I've been on I shared this song oceans. Over the past year I've been taken further and deeper than I ever imagined, onto wild and stormy seas where a few times I feared for my life. As I've reflected on this I've been overwhelmed with gratitude. I look back and see ALL the people who played a part in my treatment and recovery. I keep telling everyone that it takes a village to get you through and I wouldn't have made it without your input, support, love and encouragement. You anchored me so I wouldn't blow away in the storm. So I got this tattoo!

A reminder of all I've been through 
and all of you who anchored me through it!

You got me through and I just want to say thank you...

Thank you to all the people who showed their love, encouragement and support by sending me cards and messages, by getting in touch on Facebook, for passing messages for me onto my family and friends when I was too sick to get them in person. Every single word boosted my spirits and reminded me that no matter what I was facing there were so many people wanting the best for me. That helped!!

Thank you to all the people who prayed for me and sent me healing, good vibes and thoughts. I faced some pretty dark times when my fears and the physical trauma just about overwhelmed me. They didn't because of you.

Thank you to all the people who sent me flowers. Flowers make me happy and no matter how bad I was feeling when I saw them I always smiled (even when the chemo nausea was too bad to enjoy their scent!).

Thank you to all the people who made meals and baked treats for me. You showed your love for me through your thoughtful, delicious meals. You nourished my body and my soul.

Thank you to all the people who gave me gifts, sent me surprise parcels and left gifts on my doorstep (often anonymously). They always came just at the right time. Your kindness and thoughtfulness touched me deeply.

Thank you to all the people who visited me. I wasn't the best company but you came anyway. That means a lot!

Thank you to all the people who came and put in the hard yards sanding, plastering and painting so Holly had a lovely room to come home to (and I now have a completed nursery for my grandbaby!). Your practical help has made a huge difference to how my home looks and feels.

Thank you to all the people who drove me to appointments and treatments. Your love and support on those journeys made it so much easier to face what was ahead.

Thank you to all the medical professionals involved in my surgery, treatments and care. Our NZ healthcare system is beyond amazing. I have met the most wonderful, supportive, caring medical professionals. The oncology field takes a special kind of person - you have your wins but many losses. I owe them my life!

Thank you to the staff and volunteers at Dove House, the Cancer Society and The NZ Breast Cancer Foundation. Your ongoing support through and after treatment have helped me to keep going and make some sense of everything that I've experienced.

A very special thank you to my dear friends who were part of my post-chemo care team. You provided great comfort, lots of love and laughs when I needed it the most.

An endless, bottomless thank you to my wonderful family for your care, patience, support, long-suffering and love...
Beth and Mikey - you constantly dropped everything to come and care for me. You gave me comfort whenever I needed it and you made my dark places light.
Holly - you made it from the other side of the world (twice) to care for me with that special "Holly" kind of love that only you can bring.
Karen and Mere - who were there with me through all the highs and lows, constantly sitting by my bedside when, as Mere said, "I was one breath away from intensive care" and putting up with my blunt, confused, feverish outbursts!
My brothers and sisters-in-law, nieces and nephews - for bringing your special brand of encouragement, love and laughs.
I can never repay you all! I am so grateful. Thank you!!

Thank you to God who continues to make me feel beloved and gives me the strength to keep walking together through whatever life brings.


And just a little update on life in the real world. I got this little bundle of joy three months ago. Billie Jean McIvor - a great source of delight and laughter. I've started back at school part-time in a new role training as a Reading Recovery teacher. It's so nice to be back working with my friends and the children at school. And in about a week we welcome my grand-daughter into this world. So all in all, life is good and I'm thankful!

Thursday, February 5, 2015

yay for holidays

Early in 2014 (before I was diagnosed with breast cancer) Beth, Mikey, Holly and I planned and booked a December holiday in Melbourne. We wanted to spend Christmas together as it was the tenth anniversary of John's death on Christmas Eve. We love Melbourne and thought it would be a great place to be together to remember, celebrate and toast the best husband, father and man that we've known.

John Russell McIvor
Kind, loving, generous, supportive, honest, 
funny with a wicked sense of humour, 
a great friend and all-round good guy!

So even though I was still not feeling 100% and was wondering if I was exchanging a couch in Auckland for a couch in Melbourne, we stuck to our plan. As a precautionary measure, I did pack a variety of (legal) drugs into my suitcase just in case my health went south! Beth, Mikey and I only had a few hours flying while Holly completed a 30+ hour flying marathon to get there from London! But we all made it! We had the loveliest Christmas Eve and Christmas Day. It was profoundly moving to share our special memories and what John still means to us individually and as a family. The past ten years have gone by very quickly and excruciatingly slowly all at the same time. It seems like such a long time ago and just yesterday that John left us. We are always holding him close in our hearts.

Our annual Christmas hat photo!

It's amazing what a holiday can do! It was great to be somewhere interesting and different. It was nice to be out and about - exploring, shopping, eating delicious food, laughing and generally having fun with my favourite people. I managed to do way more than I thought could and came back home with a real boost to my spirits. This has stayed with me and has enabled me to face the next phase of my treatments with a much more positive frame of mind.

Enjoying summer fun times with ice creams!  

I have started hormone-blocking therapy and radiation therapy. The hormone-blocking is in the form of a daily tablet that I'll take for the next five years. Radiation is five days a week for four weeks, with the weekends off. Both therapies have side effects but these are very manageable in comparison to my experience with chemotherapy. And nothing beats the boost of seeing the light at the end of the tunnel, knowing that it's all coming to an end very soon. Yay!

Christmas Hat photo credit: Thomas Finn Stewart

Monday, December 1, 2014

sparkle

Well it's been a long, slow, hard journey of recovery since being discharged from hospital. After initially feeling much better being home (I think that was more psychological than physical) life settled into days of constant stomach pain, nausea and severe headaches. Resting, sleeping and endless, daytime TV were all I could manage! Things started to look up when my oncologist prescribed me some medication to deal with the stomach pain, nausea and headaches. He pointed out that I had been seriously ill and it would take time for my body to recover. He also said that I won first prize for the worst outcome for chemo out of all the patients that they've treated at Auckland Hospital this year. That in his 20 years of public and private practice he's only had one other person develop chicken pox. I am truly special!

With all this resting I've had plenty of time to reflect on life and where I'm at. So when I saw Annie Lennox on TV the other night, something about her got me thinking... She was talking about turning 60 at the end of the year, which surprised me as she hasn't seemed to age over the years. As she talked about her music and the inspiration for her latest album, she sparkled. That energy and sparkle made her seem ageless. Then I had a revelation - I had lost my sparkle! That everything I've been through this year had sucked it out of me. When I thought about it, I hadn't smiled in a very, long time and that the relentlessness of feeling so ill had worn me down to just existing. That is not like me at all. I normally try to look for the best, the happy, the joy in life and laugh heartily and loud. It has been hard to feel so low when I know that my mental wellbeing and a positive, hopeful attitude play an important role in fighting cancer alongside the treatments and therapies.

A dash of gold, glittery sparkle!

It's just as well that I have the best cheerleaders in my family and friends. They keep telling me that I'm doing so well. That I've come so far. Their love and support mean even more to me when I've been finding it so tough. I've also been given some breathing space to let the medication work, to rest up and feel better. Hormone therapy has been postponed for now and radiation therapy is now scheduled for January so I can be well enough to deal with it.

She's definitely got sparkle!

I still have a long way to go and more treatments to face but I'm starting to feel a bit better. I'm focussing on the long term picture and getting my sparkle back!


Gold sparkles - imgkid.com - the image kid has it!
Astral Double collage by Eugenia Loli. Find more of her artworks here.

Thursday, November 6, 2014

sometimes birthdays aren't easy

Yesterday was my birthday and I have to admit that it took a lot to find the heart and energy to celebrate it. I recently spent ten days in hospital dealing with serious side effects from Round 3 of chemotherapy. My white blood cell count fell really low and I developed a condition called neutropenia. Due to this low blood cell count the chicken pox virus I had as a child was also reactivated. Without white blood cells to fight it, it returned with a vengeance. Apparently this is a rare complication so it made me very ill, with rolling fevers of up to 39.9 degrees. I was in and out of consciousness continually, with mild hallucinations. Apparently I told Mere I didn't like the landscape of Rangitoto in my room because it had goblins in it. When I woke up, she said she couldn't see them. I looked really hard and couldn't see them either! My family are now regaling me with all the funny, bizarre conversations I had with them.

At one point, when they finally worked out what the spots were, I was woken up by four oncologists in full masks, gowns and gloves peering at me over the bed. I had lost all sense of reality and thought I was in a scene from the movie Contagion. It turns out I was highly contagious so they wanted to move me out of the Oncology ward as soon as possible. I was a risk to all the other patients there with low blood cell counts. So they whisked me up to a pressurised room in the Infectious Diseases ward. Everyone who treated me from then on were fully masked, gowned and gloved.

It wasn't this bad but I was hazy with sleep and fevers.
I was actually taken to the Infectious Diseases ward on a bed!

I had severe nausea and headaches and to be honest, it felt like one endless nightmare. My family took turns sitting with me during the day, which helped to separate the days from the nights. I saw at least twelve Oncologists, checking in and monitoring my condition. One thing they all agreed on was that I should not have any more chemotherapy, that the risk to my life and health was too great if I continued. I started to recover very slowly. I was so desperate to be well enough to leave. They set me the goal of eating, drinking and taking my medication in tablet form rather than needing a drip. Yay! I got there but I was still very ill when I got home. Beth and Mike were champions making sure I was well fed and looked after. I felt very loved. It was good to be home.

So even though right now I am physically at the lowest point of this breast cancer journey, feeling completely broken in my body... I can appreciate the love and support of my lovely family and friends... I can hold onto the hope of future health and wellness... I can remind myself that I don't have to do anymore chemo! Yay! That is such a relief... I can be thankful for my birthday and making it this far... I can remember and celebrate that I am beloved by so many.

I had the loveliest birthday in the end. I found flowers, treats and surprises on my doorstep. My phone and Facebook overflowed with wonderful birthday messages. I had cake with the family and a delicious dinner made by Beth and Mike. I feel so loved and blessed. Thank you!

This is not my current birthday.
I thought we'd all enjoy a flashback 
to my very, happy 50th birthday!


Biohazard suit image from Resident Evil, Sony Films
50th birthday photo credit: Rachel King

Saturday, September 27, 2014

home

Home. I've been thinking about what that word means. Yesterday we said goodbye to Holly. Luckily it's only a little goodbye as we'll see each other in Melbourne for Christmas. Not long to wait! I'm so glad we have that to look forward to... something to hold on to as I negotiate the post chemo nausea fog. Luckily it is starting to lift and life feels a bit sunnier again.

Love these guys!!

Anyway... Home...

Holly lives in London. It's her home. She came home to look after me. New Zealand is our home. I love flying home. I always get a thrill when the plane dips low over the waters of the Manukau with Auckland laid out before me. That says home to me.

Sitting in the sun at St Heliers beach watching the waves and Rangitoto says home to me.
Misty days at Huia says home to me.
The dawn service at the War Memorial Museum says home to me.
The National Anthem anywhere says home to me.
Auckland City sparkling in the sun when you drive over the Harbour Bridge says home to me.
Tuis singing in the bush says home to me.
Marmite on Vogels toast says home to me.
That snuggled up in bed feeling, listening to the rain says home to me.
The smell of fresh baking in the oven says home to me.
Summer barbeques and dinner on the deck says home to me.
Talking endlessly with friends says home to me.
Watching good movies on the couch with Beth, Mike and Holly (when she's here) says home to me.
Laughing loud with my sisters over a coffee or a glass of wine says home to me... we can pretty much laugh loud over anything!

Home - it's a mixture of place, people and feelings. Any one of these... anytime, anywhere can give you that feeling of home. What says home for you?

For me, home is these people. This crazy, funny, loud, generous, larger than life, do anything for you, love you with all their heart bunch of people... my family says home to me. Even in the midst of the toughest, hardest, saddest days they give me that "home" feeling.




Just a note: The guy at the beginning is JP from Photobooth and Moustaches and not a new addition to our family! All images were taken in their vintage photobooth.
The track is Home by Edward Sharpe and the Magnetic Zeros

Wednesday, September 10, 2014

just call me sinead

This journey is still proving itself to be a bit of a cha cha. Last weekend I found myself in hospital on the Oncology ward with a drip in my arm, an excruciating headache and nausea. It came on top of a traumatic chemo round, the allergic drug reaction and lots of adjusting and adding drugs to control my nausea. It was pretty awful. As I hadn't had dinner (due to being in A&E at dinner time) they couldn't give me anything stronger than panadol. At 2am with a drip inserted for hydration and my blood test results back they finally administered a much stronger drug. Yay! At least it took the edge off. 

The next day Mikey came to sit with me in hospital and Beth went to the airport to get Holly, who was arriving from London. I was so excited to see her but disappointed that it would be in the hospital. Not the homecoming I'd planned!! The doctors did their rounds and talked about all the factors that caused me to end up in hospital. They gave me a new regime of drugs and strict instructions on what to do to manage my nausea and headaches. They also said that since I was so sensible I could do it all at home. Yay! I was out of that hospital gown before you could say "Just relax while I insert this catheter!" (That did not happen to me but it did happen to the guy in the bed next to me.) Phew! Dodged that bullet! So the reunion happened at home and it has been the best thing having Holly here. Beth and Holly relaxed quickly into their routine of teasing me, face pats and "harden up" dialogue. Fun times!  

Mere gave me these "oops sorry you're in hospital" balloons to cheer me up.
She had wanted Disney Princess balloons but I am more than happy with the hearts!

This week I also attended a Look Good Feel Better workshop. They are an amazing charity that aim to put a smile on the face of every woman with cancer. That statement is so true. I was nervous about attending as I had still been feeling quite nauseous and unsteady. But they were so warm and friendly, they really put me at ease.  Each lady has a support person to help them with skincare and applying their make up. Mine gave me a divine facial. I must have looked pretty relaxed as the lady running the workshop said, "Well, Stacy has gone to sleep!" Either that or I had started to snore. I went in feeling below average and came out feeling revitialised and dare I say it - pretty! They do fulfil their brief "that with makeup, skincare, skills and positive attitude they can transform the look and outlook of NZ women with cancer." I left with a smile on my face and a bag full of make up tailored just for me! I felt so spoiled and incredibly lucky to be a part of it. They are such a worthwhile charity to support.


Check me out!
I think I look pretty damn good!!

Later that day, my hairdresser Alice, Beth and Holly joined me for the big moment... to shave off my hair. Hair loss is a side effect of the chemo that I'm having. They say it starts round Day 14 after your first dose. Mine hadn't really been doing much except for the usual handfuls that fall out on a regular basis. It's the anticipation and waiting for it to happen that can be distressing, then the actual clumps of hair on the pillow themselves. In an attempt to gain back some power in a situation where I've been pretty powerless, I decided where and when my hair would come off. At home with my lovely hairdresser and my beautiful girls, with laughs, teasing, love and moral support. Losing my hair has been quite a big thing for me, more than I had realised. For my whole life I've said something about who I am with my hair. To not be able to have it and to have to wear a wig have been big things for me to come to terms with and grieve over. You might think it's just hair but it's part of my identity. Choosing how my hair loss would happen has made that grieving easier. It actually turned out to be fun and there were no tears!! Yay! I was also very honoured that my nephew Josiah shaved his head to support me. So now we are baldy buddies!


The girls all think I look quite like Sinead O'Connor.
 So instead of inflicting my photo on you
I'll leave you with Sinead!

Saturday, August 30, 2014

a side of daffodils

It turns out that I can pretty much have adventures wherever I am. I don't need to look for them. They just seem to find me...

On the morning of my first chemo round I nervously approached the Oncology Day Stay Unit. The staff were so lovely. They are very welcoming, trying to put you at ease, especially when it's your first time. You can tell the newbies - we still have our hair! I was set up in my comfortable lazyboy chair. Beth and I were greeted by the other patients and their support people. Everyone is so friendly. There is a real sense of camaraderie and support, that we're all in this together. Finally I was settled in and the morning was progressing well. Beth wandered up to the cafe to get me some treats and everything seemed to be going to plan. I was feeling way more relaxed. This was not as bad as I thought it would be... 

Apparently about 5% of people are hypersensitive to the chemo drugs. It turns out that I am one of them! After a while the sensitivity kicked in followed by an allergic reaction to the drug they used to manage it. I felt like I was going to black out. My usually low blood pressure and steady heart rate shot up. I was so shaky with the shock. Suddenly it was how many medical professionals can you get in one room? 

So while the other patients are sitting peacefully receiving their chemo and chatting quietly with their support people, I'm all sobbing and fainty with 25 medical staff around me! Not the day Beth and I had envisioned!! Eventually everything calmed down and I resumed chemo with the second drug, which proved to be absolutely uneventful. Whew! Our lovely friend Zoe had arrived at the height of the madness with a beautiful corsage for our chemo date. Finally I was able to put on my corsage and enjoy the fine company of Zoe and Beth.


It was a long day. You know you've stayed too long at the party when they start stacking the furniture and mopping the floors around you! We gathered up our things. Beth went to get the car and I made my way to the door. The Cancer Society had left bunches of daffodils there for people to take home. So when Beth came back to get me, she found a shaky lady by the door holding a bunch of daffodils in one hand and a bright yellow Cancer Society balloon in the other! 

The perfect ending I think... Round One of chemo with a side of daffodils.

Daffodils in Wellington for Daffodil Day.
Please support the Cancer Society here.
They give us all hope!

Tuesday, August 26, 2014

place to be

This song has been resonating with me lately... 


When I was younger, younger than before
I never saw the truth hanging from the door
And now I'm older see it face to face
And now I'm older gotta get up clean the place.

And I was green, greener than the hill

Where the flowers grew and the sun shone still
Now I'm darker than the deepest sea
Just hand me down, give me a place to be.

And I was strong, strong in the sun

I thought I'd see when day is done
Now I'm weaker than the palest blue
Oh, so weak in this need for you.

Chemo starts tomorrow. 

So I find myself...
darker than the deepest sea,
weaker than the palest blue,
looking for a place to be
and in need of you.

I am seeking God's embrace.

A lovely friend sent this verse from Psalm 94 to me.
When I said "My foot is slipping," your unfailing love Lord, supported me.
When anxiety was great within me, your consolation brought me joy.

Just breathe...

Monday, August 18, 2014

the cha cha

The last few days have been a rollercoaster of emotions. In the weekend I got the heartbreaking news of a helicopter crash in Wanaka that killed this lovely, generous, funny man who had a zest for life, his family, his friends and his faith. He was on a weekend away with good mates, several of them were also injured in the crash. The impact of this shockwave is resonating through the St Paul's community.

Jerome Box
A man who lived life to the full.

John was Jerome's quantity surveyor for many years. I can just see them sitting down so many times to discuss life, families and faith, not just the work at hand. I can see Jerome's wry smile, hear his chuckle and listen to him share his unique take on life. My heart is aching for his wife Adelle and their gorgeous children... and the other injured and their families. It's shocking when the tragedies of the national news actually rock you and the world of people you hold dear.

Then I had my Medical Oncology appointment. All throughout my diagnosis and treatments every medical professional has told me that I don't need chemotherapy. That for the grade and stage of my breast cancer, surgery and radiation therapy will be enough to effectively treat it. That I will need hormone therapy to suppress the estrogen that feeds the cancer cells (in the form of a daily tablet) but no chemo. I thought the appointment would be straightforward. "Here are your results, here's the prescription for your hormone tablets, good luck with radiation therapy next week..." I became suspicious when the oncologist said I'm going to discuss your options for treatment. It turns out that the pathology from the surgery shows that my tumour is Grade 2 and not Grade 1, so now chemotherapy is part of the treatment to improve my chances that the cancer won't come back. Usually in journeying situations an upgrade is much appreciated. Who doesn't want to fly business class or have a better hotel room with a lake view? On the breast cancer journey an upgrade doesn't have the same desired effect!

I just didn't think I would have to walk this road and now it's right there. Chemo starts in two weeks. So in preparation I got my nails done, shared a bottle of bubbles with my long-suffering, very supportive sisters and made an appointment with my lovely hairdresser Alice Tucker for a last cut, colour and style before it all goes.

My dear friend Em (who is on her own breast cancer journey) shared this picture with me after we talked about the difficult, discouraging forwards/backwards nature of our journeys so far.


So here I am doing the cha cha, trying to keep a lightness in my step, with a heavy heart and tears streaming down my cheeks.  The great thing is I am not dancing alone, you are all here with me. So grab the ones you love, who are precious to you and let's dance!

Tuesday, August 12, 2014

exposed

Yesterday I had the planning and set up appointment for radiation therapy. It involved a CT scan in the position that you receive the radiation treatment and the application of permanent tattoo dots onto your skin. These dots enable the machines to line up perfectly each session. You spend a lot of time physically exposed while three people move you and your breasts around - taking measurements, drawing on you and taking photos. Everything is recorded in detail so the delivery of radiation is perfectly placed - quickly and efficiently. I'm so grateful for their thoroughness as I want every opportunity that I can get to make sure this cancer doesn't come back.

The radiation therapists were lovely. They were kind, reassuring and very professional. Despite this care, I have been left with a feeling of vulnerability and exposure that goes way beyond skin deep. I've been thinking about why I feel this way. With a diagnosis of any kind you feel that the power to have control in your life is taken away. Suddenly you are being swept along into surgery and treatments, results and consultations, medical data and statistics. It overwhelms you emotionally, mentally and physically. I'm also a pretty private person and up until recently only a very few, select people have been lucky enough to see my breasts. Now so many people have seen (and examined) my breasts that I have lost count!

It got me thinking about a summer I spent as a teenager at Muriwai Beach. It was all fun and games until I was picked up and dumped by a wave. As I dazedly came up out of the wave, I belatedly realised that the turbulence had caused my bikini to rearrange itself and I was... ahem... exposed to an appreciative audience of surfers waiting for a wave! Ooops! 

Beautiful Muriwai Beach 
Those waves look deceptively calm from a distance.

So whilst wanting to engage fully in every aspect of treatment that gives me a better chance long term, it is much like my teenage experience of being unexpectedly dumped on Muriwai Beach... I am feeling shaken, vulnerable and exposed.

This sign was not around when I was a teenager.
That is me being thrown around by the wave. 

And to those lucky surfers I just want to say, "You're welcome!"

Tuesday, July 29, 2014

something funny

Anyone who knows me really well will tell you that I have a cheeky, naughty sense of humour. I can be funny by accident and just embarrassing (to those around me) when I try to be funny. I thought in light of my recent hard, emotional posts that I would share some things that I have found funny on my breast cancer journey.

On the morning of my diagnosis I was very nervous and worried. I put on my Gorman vegetable dress - my "happy" dress. Whenever I wear this dress it transforms how I feel. It's fun, colourful and the print is full of vegetable surprises!


The Gorman Vegetable Dress
These are not my arms.

I put on the dress and I already felt better. If it was going to be bad news I could take it in my happy dress. I started to put on my make up and because I was so nervous I didn't really pay attention to how much I was putting on. Apparently there is such a thing as too much make up for a cancer-related medical appointment! Beth came to pick me up and when I got into her car she said "Muuuum, don't you think you've gone overboard with the make up?" I had evening eyes and evening lips for a medical appointment at 9 am in the morning. So the car journey was spent wiping off the excess eye shadow and replacing the bold lip colour with a nude shade of lip gloss. At least I wasn't worrying about the diagnosis!

The day before my first surgery, I had an awful procedure that involved several very painful injections of radioactive dye into my breast. The radiologist delivering the injections was a cheery man wearing a Cookie Monster tie. That did make me smile a little through the pain. Does a sunny disposition and a Cookie Monster tie make it easier to carry out tortuous procedures?

When having surgery you get to wear one of those attractive surgical gowns that open at the back and a front-buttoning cotton dressing gown over the top. It's generally one size fits all. Being short they cover me to well below my knees. I feel so attractive swathed in voluminous folds of well laundered cotton, stamped with hospital property (to deter you from wearing them home I guess). A pair of white knee-high pressure socks complete the outfit! Perfection!

 Yup this pretty much sums up the hospital gown. 
This is not me but I know how he feels!

Once again I was feeling very nervous with all the prep before surgery. They have these great lazyboy-type chairs for you to "relax" in. So I was trying to still the nerves and relax with my feet up when the nurse called me in for a consultation. I clicked the side handle forward and nervously jumped up to meet with her. Unbeknownst to me, I had caught the folds at the back of my gowns in the footrest. That pulled me up short real quick with a loud involuntary exclamation (luckily not an involuntary swear word!). I made Beth and the rest of the waiting room laugh whilst hopefully relieving the pre-surgery tension for others.

My other surgical gown-related incident was the obligatory back flash to the lady in the bed opposite me as I shakily got up to use the bathroom for the first time after surgery. I'm so thankful that I was wearing underwear so it was better than it might have been!

When John was sick we coined the phrase "Kiss My Butt Boy" which was a lighthearted way of saying you're really, really sick and we will do anything for you, anytime. Well my stint as "Kiss My Butt Girl" only lasted a few days. It was abruptly drawn to a close when I showed Beth I could wave my arm and was told I could get up and make my own breakfast since I was feeling so good. Darn! Too soon! Too soon!

Today was the first day in a very long time that I woke up with that "I feel good" feeling. Yay! It's amazing to remember that I can feel like this. I still find the ups and downs and forwards and backwards of this cancer journey difficult to deal with but smiling at the ironies of life and having a laugh in the midst of it all helps me to keep going. 

Gorman image from www.gormanshop.com.au
Walter White resplendent in his hospital gown, Breaking Bad, AMC

Friday, July 4, 2014

expect the unexpected

I've been on this breast cancer journey for a few months now and I would still rather be going to Paris! I had my surgery two weeks ago and it went really well. I survived the several painful, invasive procedures in preparation for the surgery, then the surgery itself. Apart from my normally low blood pressure finding new depths to fall to, I felt much better than I thought I would. Preliminary tests showed that my lymph nodes were clear of cancer and that the tissue they removed with the tumour was all clear too. As everything had gone well I was allowed to go home the next day. It felt so good to be home, to sleep in my own bed, to sleep deeply without being woken up to see how I was sleeping!


I was so happy. I felt like a big weight had been lifted off me. I had completed the first hurdle and the relief was incredible. I've been resting, sleeping, healing, reading, quietly crafting while watching endless episodes of the Gilmore Girls! I have been cocooned by the love, care and prayers of my gorgeous family and friends. I've been feeling grateful, feeling peaceful, feeling relieved, feeling I can get through this...

Then I had my post surgery appointment with one of the specialists from my medical team. They gave me the definitive lab results of the lymph nodes, the tumour and surrounding tissue that they removed. My lymph nodes were still clear but because my cancer is the spreading kind, they felt that the margin they had taken on one side of the tumour was not enough. I knew that there was a possibility of things showing up that they hadn't picked up in the surgery. Maybe I would need chemotherapy. I had expected a time for radiotherapy to start. I did not expect that I would need more surgery, that news completely floored me. They are looking at the long term, that I have the best chance of the cancer not coming back. I want that chance!

So while I'm grateful for the expertise and diligence of my medical team, I once again find myself feeling the weight of my grief... needing to find the courage to keep engaging in the nature of this cancer journey - walking two steps forward, four steps back... learning to expect the unexpected!


Tuesday, June 10, 2014

oceans

Well it's been a while. Two years since my last post! That feels very confessional! Sometimes life just becomes busy and some things (like this blog) fall away. But it's always been here waiting...

Lately I've found myself walking some familiar paths that I didn't think I would return to. It's made me stop, take a breath, look around and to be very present in what is happening in my life right now.  About a month ago I went for a routine mammogram. I always find them a bit worrying because my sister Karen's breast cancer was picked up on a routine mammogram... I am also the same age as her when she was diagnosed. So when I got a call back to say that there was an area of concern it was hard not to let that worry escalate. Back for a physical exam, mammograms, an ultrasound and a core needle biopsy. Things were starting to look not so good.

So at exactly the same age as my sister, on exactly the same day four years later I was diagnosed with breast cancer. Such a weird coincidence! I have a small Grade 1 ductal carcinoma in my left breast. Apparently if you're going to get breast cancer it's the best one to get! It's been caught early and my prognosis is great. Next week I am having a partial mastectomy and if there are no complications, radiotherapy treatment when that heals.

So those are the facts. The emotional and psychological backwash of this diagnosis is harder to describe. I have walked alongside the most precious people in my life as they have had to come to terms with the ravages of life (and sometimes death) with cancer. It has been a heartbreaking experience over and over again. It takes all you have and then some. I never thought I would have my own cancer journey. This has been a surprise!

Yet here I am, walking this path. As the specialists have said, you are just starting your breast cancer journey. I was thinking if I was planning a journey I would rather choose Paris as my destination! I have found it all a little overwhelming. I bring all of my other experiences of grief and loss to this, so the weight of it is very real. While I am SO grateful and thankful for an early diagnosis and a great prognosis I have some tough things to face in the next little while.


Some people have said "Why you? You've had enough!" and you know I just don't think that. I think why not me - life happens, it's not always what we choose. Sickness, cancer, death, accidents, whatever... they're all out there. I know that I have to face whatever I have to face and want to find the strength and grace to walk through it with courage and dignity. (Well as much dignity as you can have in these situations!) A lot of people are looking at, poking, prodding, cutting and stitching up the most sacred of things - my breasts!! I feel an incredible sense of God's presence. I talked here about my Beloved tattoo representing how I feel about God and how God feels about me. I know I am his beloved. We're walking into this together. 

My family and friends are amazing, showing me time and time again that I am loved and not alone in this. My poor family walking through this again! My beloved girls Beth and Holly, my lovely, lovely son in law Mikey, my sisters Karen and Mere laughing and crying our way through this together. I am beloved. I am blessed.


And in case you're wondering why this post is called "oceans", I've played this so many times. I have found this song to be immensely moving and comforting as I find myself out in deep waters needing God's presence to lead and sustain me. 



Thursday, June 21, 2012

blue skies are calling


This is a song for anyone
With a broken heart
This is a song for anyone
Who can't get out of bed

I'll do anything
To be happy
Oh cause blue skies are calling
But I know that it's hard

This is the last song that I write
While still in love with you
This is the last song that I write
While you're even on my mind

Cause it's time to leave
Those feelings behind
Oh cause blue skies are calling
But I know that it's hard

I don't think that it's the end
But I know we can't keep going
I don't think that it's the end
But I know we can't keep going

But blue skies are calling
Oh yeah blue skies are calling
Oh blue skies are calling
But I know that it's hard


I love this song by Noah and the Whale. It resonates in my spirit. I feel like I've had to say a lot of permanent goodbyes in my life - to my Mum and Dad, John's Mum and Dad and of course my beloved husband - John. I feel like I've had my fair share of dealing with the emotional and physical toll of cancer on the people I love - with my Mum, John's Dad, John's melanoma, my sister's breast cancer (now in remission. Yay!). There's been a lot of sadness, a lot to process and deal with.

This year has been a funny year so far (not the haha kind). I've spent six months with a stress related illness that is taking a long time to come right. I've said "goodbyes" to my precious Holly as she's spread her wings and flown to England. I am so happy for her, with lots of exciting adventures ahead. But now I'm finally living alone and working out what that's like for me. I've had times of feeling really lonely (even though I've got 262 Facebook friends!!) and it feels like a time of transition. To what... I'm not sure!

I'm optimistic for the future... pondering what's ahead... cause blue skies are calling but I know sometimes that it's hard...

Tuesday, September 28, 2010

losing someone....

Recently I was asked to share "what it's like to lose someone to cancer" at a cancer information evening. A great title for a talk! This is what I said......

Hi, I’m Stacy and my husband John died of melanoma cancer on Christmas Eve 2004. Woah! That’s ages ago you might think but there are aspects of that event that resonate with me today. So I'd like to share a little bit of my story....

John’s cancer happened in two blocks - with his initial diagnosis and treatment in 1995 when he was 36. He had a referral to a melanoma specialist to check a large suspicious looking mole on his back. At the time I thought – don’t panic, don’t make it bigger than it is, it will be okay, nothing will happen to us, God’s got it under control..... I played it down in my mind as a way of coping and not giving in to fear. When John came home and said they’re 98% sure it’s a melanoma, I didn’t really react as I thought.... it won’t be, it’ll be okay....


He went in for surgery to have it removed with a large elliptical margin around it and it wasn’t until they came back with the histology that I finally reacted. The flood gates opened, I was sooo fearful and shocked. He needed further surgery and the prognosis was not good. It was a very large melanoma and it’s size meant John had a 70% chance of dying and a 30% chance of surviving. All cancer diagnosis eventually comes down to statistics – rates of survival, development of the disease... They can be frightening, overwhelming and ultimately unhelpful. We found we had to pray and really listen carefully to hear God’s voice in the midst of it all. And we did. John recovered from his surgery, he went in for checkups, had countless numbers of moles removed and we began to feel optimistic for the future. John always said “I dodged that bullet!”

Then in 2003 he was officially pronounced clear and was discharged as an outpatient. Yay! But then in September 2004, on his 45th birthday, he felt ill. Like he had gastroenteritis and he progressively began to feel worse. At first we thought it was something fairly normal or routine but as time went on, we started to put the dots together. A diagnosis from the specialist confirmed that John was suffering from end stage melanoma cancer, too late and advanced for chemo. He was pretty sick by then, riddled with tumours in every part of his body. And that was when our long dark night (as John called it) began.

I took time off work to be his full time nurse which was an amazing privilege and it made it much easier for him to bear everything. The thing about that, is it starts to wear you out. It’s a constant pressure emotionally, physically, psychologically and spiritually – it’s exhausting. My family were great, stepping in to help out where we needed it. It’s such a weird time - helping someone you love so much and actually don’t want to go, to face death and to die well. To try to ease the way in any way that you can. You feel like you’re in a bubble with the muffled outside world whizzing by. It’s emotionally charged, overwhelming, beautiful, meaningful, special, heart breaking, awful and terrible all at the same time.... and you wouldn’t miss it for the world.

John knew he was going to die. He knew the path God had prepared for him and what he was asking of him and he never flinched. He concentrated on finishing the race. He told the doctors, “I have no regrets. I wouldn’t have done it differently. I have lived a full life.” He felt immensely blessed, he talked to everyone about his faith in God. How he could face death without fear because he knew where he was going and that Jesus would be with him.


On the day he died, he said to me, “What’s the plan today, Stace?”
And I said “You’re going to get through today and finish the race.”
And he said, “I can do that.” And he did, John finished his race well.

In the early evening of Christmas Eve 2004, the room was very peaceful with a soft, golden light. There was a tangible presence of God in the room, strong and comforting. The girls and I were with John, waiting.... Beth saw John open his eyes and look up, like he was looking at someone. She said, “Mum!” We looked at John, he took two breaths and then he died. One step from here to eternity... John lived and died well. We knew God was saying, “Well done, good and faithful servant.”

Knowing John, his faith and the life he lived, gave us hope in the time of his sickness and death. We knew it wasn’t the end, that he had finished the race, he was with God, totally healed and complete in him. The night before he died, he said to the girls, “It’s not good bye, it’s see you later!” So for us, we know we’ll see him again. That has been a great source of hope in the midst of our grief.

Several hours after John died, I went into shock. I couldn’t stop shaking and I felt physically ill. My mind stopped functioning properly and I felt completely overloaded. That’s when the long dark night, turned into overwhelming darkness. I knew that it would be hard when John died, but I had no idea how hard. The pain was physically, mentally, and emotionally overwhelming. Sometimes I felt I couldn’t take anymore, it was more than I could bear.

I kept going through the days between John’s death and his funeral. There were things to organise, think about, people to talk to, flowers, venue, catering, music…… I just kept going – mentally and emotionally stretched. I felt God beside me, so close.... helping me, holding me, bringing me through. John’s funeral was amazing. Full of love, tears, laughter, praise, honouring God and John’s life. So many people came. Then we were alone.... starting to learn to live without John – my best friend, buddy, love, mate, partner, husband, rock, encourager, my girl’s amazing, funny, reliable, encouraging friend and Dad. There was such a space, a gap, a void, something so precious missing from our lives.

I walked with John into the valley of the shadow of death – he walked out through to the other side into the fullness of God’s promises for him. I stayed there in the valley, stuck in it’s long dark shadow. The walls of the valley are steep and the shadow is big, long and black. In the depth of that valley the darkness is overwhelming. I would have been overwhelmed if I hadn’t felt God close beside me, holding me up, giving me strength, feeling the pain and helping me to bear the pain, weeping with me. Whispering in my ear “I can get you through this.”


He will never give me more than I can bear. 1 Corinthians 10:13
God is my refuge and strength, an everpresent help in times of trouble. Psalm 46:1
Jesus was a man of sorrows and acquainted with grief. Isaiah 53:3
I held onto those scriptures. They were my lifeline. They gave me strength to face each day, to take one step forward, over and over again. I have been through such times of unbearable loneliness. I have cried oceans of tears. I have felt strung out, wrung out and completely physically, emotionally and mentally exhausted. I just kept turning back into God, nestling into him, sheltering under his wing, hiding myself away.

I felt so small, like a little child facing the world all by herself.... vulnerable, unsure of her place and purpose. My heart was broken – my baby was gone and the pain and impact of that was indescribable. People asked “Did I miss John?” I ached for him with every fibre of my being. Missed him, that’s an understatement!

I felt like I had no future. My future, my hopes and dreams had died with John. Part of me died with him. My world was completely black. I’ve always tried to look at life from the glass half-full perspective, looking for the positive, the good in every situation. Now I felt like someone had taken the glass, thrown it away and completely smashed it.

I held onto the scripture Jeremiah 29:11 “For I know the plans I have for you," declares the Lord, "plans to prosper you and not to harm you, plans to give you hope and a future.” Every day I would say that over and over again. In my head I knew it was true but I didn’t feel it in my heart. I felt like I had no hope, that it was completely gone. It was my statement of faith to God. I know you have good intentions for me and I am going to keep holding this up to you because you are faithful. Sometime, somewhere in the future, something is going to happen.

And through it all God kept close beside me as I was walking, trudging, climbing, falling, stumbling, trying to find my way. My story is not that I’m incredibly brave or strong or amazing or an awesome woman of great faith but that in my mind-numbed, broken state I just kept turning back into God.... that every day I would choose to take all my pain, my hopelessness and give it to him. That I would take one step at a time, one after another, after another, every day.... choosing God, believing that he had good things in store for me... that he could get me through this.


Someone said to me that it would ease after about a year but it didn’t. My world felt completely black and hopeless for a long time. After two years I felt the darkness start to lift a little, turning my world to shades of grey. I felt like I had finally climbed out of the valley of the shadow of death and could see a little light. But it was still grey. It wasn’t miraculously over but there was a tiny seed of hope.

In going through the darkness and pain, I felt that God wanted me to feel the depth of my loss and my grief. To let it resonate fully through my heart, mind and spirit. To know how much I have lost, how much I missed John, to acknowledge how much my life had changed, to feel my broken heart, to fully experience all the feelings no matter how painful and to let God into the midst of it all to begin healing me.

And all along the way God sent me people - my amazing family and friends and sometimes even strangers got alongside me, encouraged me and helped me to keep moving forward when I felt like giving up. They loved me regardless of how I was, they prayed for me, encouraged me, gave me words of wisdom, fed me, hung out with me, carried me, poured me a wine, cried with me and laughed with me. And there were times when I thought I’d never laugh again (and I am normally a pretty funny person). They let me just be me. They let me process things at the pace I needed to. My beautiful girls put up with a lot through all of this. They are my most loyal supporters, cheerleaders and friends. And my family, my gorgeous sisters were amazing. We often talked about hunkering down, wagons in a circle, protecting each other like in the Wild West!

I’m still on a journey with my grief. As I’ve walked through the darkness, I’ve fully experienced the depth and power of God’s love and his healing power in my heart and life. Through death and pain, I’ve found a new life with depths of compassion and love that somehow make me a richer person. I’ve found a life with hope!

I’d just like to finish with this thought - cancer has taken a high toll on my family. Eight months after John died, my Mum died suddenly of undiagnosed bowel cancer and at the moment I am supporting my sister through treatment for breast cancer – she’s had a mastectomy and has just finished chemo. And yet in the midst of it all we still love God, we press into him for comfort, direction, encouragement and support. We see his healing hand working every day....


....and we are still standing strong. So in all of that cancer has not won!


Know Hope by Michael J Totten
Hope by Jake Belder
Your Existence by Ashley MC
Graffitti Heart by 55Max

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