Monday 29 August 2016

Weekly Discussion Summary ~ Stronger

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Why is the word stronger highlighted? Because, 'stronger' is an obscure word, ambiguous and highly context dependent. To break down in the face of traumatic experiences is normal - if we lose a loved one, if we are diagnosed with cancer, yes, we become depressed and distraught. This is a normal reaction. So do these reactions then mean we are not strong?
How can we define strength in such circumstances?

Resilience is the way by which we rise rising from the point of breaking down. Resilience is not about being tough and numb, and avoidant. The first step to practicing resilience is acceptance and embracement, and to accept means to show flexibility in how we decide to engage with the trauma. This is the opposite of avoiding and turning away. Strength is the flexibility by which we engage with trauma, learn from it, and choose to be resilient.

We discovered that this is an incredibly hard practice, because it is so much easier to avoid, ignore, and inhibit and bury the source of trauma because we fear it may define us, limit us, and belittle us, hold us back and ultimately make us a victim to it.

#ResilienceDiscussion


Thursday 25 August 2016

My view of life through cancer-tinted glasses ~ Caroline

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As any person who has ever had cancer will tell you, once you hear that fateful diagnosis, your life is forever torn in two - life BC and life AC. There is no going back.  They say cancer changes you, but what if you didn't know who you were BC?  I know what the name on my birth certificate says, but who is Caroline and what makes me different from everyone else?

I am a daughter, sister, wife, mummy, runner, triathlete, vet, cancer patient, vegetarian, but those are all things attributed to me rather than me per se.  Maybe I should be grateful that cancer has given me a greater degree of self-awareness than I ever would have found on my own.  Without a doubt I have a different outlook on life than I did BC, my values have changed and as I search for meaning and a sense of purpose I find myself looking inward.

As I do so I look at all my relationships and what they mean to me. I finally understand that change has to come from within, and in doing so accept that certain relationships are probably never going to change.  That acceptance brings me a sense of peace that has been a long time coming.

I am the master of my own fate.

Cancer is now part of who I am. There is no escaping it, especially since my last appointment where I was told the family history clinic would follow me for the rest of my life. There will be no returning to the way things were, no end to the appointments.  The mention of the family history clinic brings a renewed concern about the genes I've landed my children with, and thoughts about when I should broach the subject with them.  Not yet, they're too little, let them enjoy a worry free childhood for a few more years, as long as I remain NED (which stands for no evidence of disease, a delightful phrase uttered by oncologists who will never declare me cancer free.)

I read something the other day that described the first year post cancer treatment as the 'tofu year.' This made me laugh as I have stopped eating meat and dairy products, and do enjoy a smoked tofu salad or an iced soy latte. I am not so keen on green tea, and as I believe you have to drink 7 cups a day for its cancer reducing properties to have any effect, trying to force 1 cup down my throat every now and then seems a bit pointless.

I will never know why I got cancer. Yes it runs in my family, but that still doesn't explain why me instead of my sister or my cousins. But equally why not me? I have no idea if changing my diet will reduce the risk of my cancer returning, but I have read several books and scientific studies that point towards a western lifestyle as being a contributory factor to the huge rise in levels of certain cancers over recent years. I do feel healthier, and more importantly I feel like I am doing something - the doctors have done their bit, now it's my turn.  I am no saint though. I still enjoy a glass of wine as much as the next person, and will never give up my morning coffee.

When I was first diagnosed and going through treatment I never questioned why. I told myself that it was all down to bad luck, and that I didn't have the energy to answer the unanswerable.  I now know that I was quite naive to think that I would be OK with that as time went on. I have spent the past year asking myself that question in so many different ways. I have searched my soul, dug through my past, meditated on it, and finally am back at square one being unable to answer it, but I have reached a level of acceptance that I could never have achieved without having done the work.

I also think I'm OK with the idea of a recurrence, but of course I'll never really know unless it happens. I don't know why I'm so convinced that it's only a matter of time before the bast*rd comes back, but at the moment that's where I'm at.  Maybe as more milestones pass by, 2 years, 3 years, 5 years, I'll have more faith in my body's ability to stay healthy.

Meanwhile I shall continue to search for answers to my many questions, in the knowledge that cancer has given me increased clarity about who I am.  Cancer itself hasn't changed me, but it has given me the impetus required to make long overdue changes.


In other news, do you like my new cycling socks?


Wednesday 24 August 2016

A Deadly Inheritance - Leaning To Live With Hereditary Breast Cancer ~ Tamsin ~ HuffPost Blog

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"It’s March 2011. “I’m sorry, you have a BRCA1 mutation,” says the Genetics Consultant. I’m not expecting this news."
We're so proud to share Tamsin's recently published post for HuffPost UK where she talks about how she's learned to live with her hereditary breast cancer.
We're especially thrilled because up until April 2016, Tamsin had only ever written a piece for the YWBC blog. With encouragement and support, she's developed her technical expertise to blog and the confidence to find her voice. We hope that Tamsin's experience will inspire anyone who might be reading this post wondering whether they could write.
Please do contact Vicky, Tamsin or Naz if you would like to submit a post. We'd love to hear from you! xxxxx
Submissions can be emailed to: bcresilience15@gmail.com
The blog address is: http://www.bcresiliencecentre.blogspot.co.uk/




http://www.huffingtonpost.co.uk/tamsin-sargeant/a-deadly-inheritance-lear_b_11603742.html

Wednesday 3 August 2016

Are We Ever Really 'Cancer Free'? ~ Amanda

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Getting fed up by my mood swings. Why don't I talk about it anymore they ask, because I'm really fed up with the topic of cancer I say. It feels like everyone has cancer or has had cancer or knows someone who has. Friends dying and friends relatives too. I really try not to be negative about it and I don't want to be a bore, but it's very hard trying to stay positive. So I'm up and down like a yo-yo!

There are survivors out there who really do walk on sunshine for the rest of their days, run marathons and savour each day. I really do try to walk on sunshine most days. But there are days I feel that I have somehow failed for not being all inspirational.

I don’t know if I have cancer cells hiding, waiting to mass again. But I'm a healthy vegetarian and I manage short walks to keep active, within my current pain levels.  All I know is that I am holding steady in a state called "No Evidence of Disease".

I have been told that everything looks great on all my blood work, and my tumour marker is low. But I immediately began to punish myself for everything I’ve done wrong as a survivor, including not eating a clean, sugar-free diet, not doing triathlons, and not being super positive at all times. Even though I know all of that is no guarantee that my cancer won’t come back.

I've had a few scans and “No evidence of disease,” my Oncologist said!  I live a pretty great life, and should be on top of the world!

Death stalks us all, that’s the nature. Maybe survivors are just a bit more aware of it. I cope with short walks. I cope with making fun out of my Franken-tits!  I cope by actively redirecting my thoughts, or so I think, or am I just in plain denial. If I don’t cope and just feel sorry for myself, I just go under and hit the depths of depression and anxiety I'm trying to avoid.

Still, it’s good to complain about being a survivor. I can complain and I will complain! And then, having done so, I will shrug and say, but seriously, it could be worse.

Positive thinking got me through Cancer and I aim to make it get me through life.


Originally posted on Amanda’s own blog on 20th June 2016:


Thursday 21 July 2016

Getting Ourselves a Strategy ~ Jackie

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I used to think that resilience was in small part developed over time, in the, 'What doesn’t kill you makes you stronger' school of hard knocks, and in huge part, hereditary. Some people are born with the ability to head-butt the knocks out of their way aren't they? And some people, well, they find it harder.

I've always considered myself quite lucky to have a fairly hard head. People would comment that I was strong, resilient, positive and I just thanked them kindly and thought that a few of life's little boulders had served me well and the rest, well it was just how I was made.

I've changed my mind somewhat.

A year of Tamoxifen, and it was playing games with my body. The result was that I had a hysterectomy and oophorectomy (doesn’t that sound like an enormous kick up the backside?) but for the uninitiated, it's when your ovaries are also removed. I suspect that many people reading this will already know that.

I was ready for this hysterectomy. Hell, I'd had cancer! This hysterectomy would be a walk in the park. There was a 50% chance the surgery would be keyhole. I'd find out whether it was this, or the more invasive stomach incision, after the op. Frankly, I was knackered and I crossed my little fingers that keyhole surgery would be possible and saw the operation as my chance for a bit of a rest. I woke to the wonderful news that it had indeed been keyhole and thus looked forward to four weeks of reduced work and increased reading. I admit, I was a little giddy at the prospect.

The surgeon and I had discussed hormones. With chemo and Tamoxifen in my back pocket, the hormone effect shouldn't be too difficult to navigate; my body was used to it. It had done the premature menopause thing through my treatment - albeit a 'fake' menopause -  and thus this would all be easy-peasy for a body used to incapacitated oestrogen.

So I wasn't expecting the volcanic effect on my hormones.

I can safely say that through all the good, bad and ugly stages of my life, I have never been so badly affected by hormones. I have never felt so physically and emotionally down, so helpless, so desperate.

And so shocked. I really hadn't seen this coming.

I can only equate it to living in a perpetual out-of-body experience. My brain was telling me that it was being ridiculous: this wasn't real, no way did I feel like this, hormones were entirely to blame. And yet my brain was also behaving as if it was very, very real, making me cry, question everything, hate myself and fear stepping out of the house. It felt so real, I felt so desperate, it was so unusual, it was quite terrifying.

But please stay with me, because it gets better.
The six weeks post operation taught me something about resilience. It isn't simply about how hard your head is, everybody gets a curve ball now and again which hits them where it hurts. What I learnt from this almost surreal period in my life was that more than a God-given hard head, we need a strategy.

This was mine:


1. The Mirror
In the early days of cancer, I used to look in the mirror and – please excuse me for a moment because I'm not someone who swears but this was really the point – I used to screw up my eyes, put on my best cross face and say, 'F*** off cancer, you little bast***, you're not having me, you're pathetic.' It worked. I'd walk away from the mirror, amused and empowered, and this would dissipate some of the fear until it lurched back again. And then I'd repeat the process.

I decided to do the same. I knew the terrible gloom wasn't real but telling myself that hadn't been powerful enough. So I went back to the mirror, looked myself in the eye and said to myself over and over, that, this was me. I am not that hormonal monstrosity sitting in blackness in the chair. I told myself this until it stuck. I told the hormones to 'f-off', they'd never beat me. I'd beat them. Granted, this sounds like some 10p second hand self-help book from a sales-driven unheard of psycho-babbling guru - but try it. Honestly, it really worked for me.

2. Endorphins
I've always loved sport. I went to a dreadful school academically but it had the most wonderful PE teacher and it all started there. I've known the endorphin rush from running for many years. I know that running, and to a lesser extent other sports, keeps me on the hormonal straight and narrow. For six weeks after surgery I wasn't allowed to run which certainly wasn't helping my sorry state. One day, when the last thing I wanted to do was organise a coffee with friends but knew this was exactly what I should do, pretending everything was absolutely normal, I texted some of my closest allies. I was on a driving ban after the op but I politely refused offers of a lift the one mile down the road to the café, opting instead to walk three miles on my own. I'd walked most days since the operation with the lovely husband and it was good to be out of the house but those had been strolls. I'd benefited from the fresh air, taken in the wonder of the beautiful bluebells, thanked my lucky stars I had him by my side, but it hadn't done anything for the endorphins. This day I didn't wander but, instead, I paced the three miles to the café. I could feel my heart beating faster than it had for days, and could almost touch the darkness – temporarily – leaving.  It was enough to know that if I could engage the help of my endorphins, the hormones would meet their match. In short, I needed to walk - and at a pace.

I continued walking, faster and faster every day. And I even logged my mileage – it wasn't much, but there was enough to feel I'd done something to take back control and that was empowering in itself.

3. Help
I'm quite an independent soul. I don’t often seek advice from people, prefer to sort things out in my own head. I find that when I talk about difficulties I, 1. feel guilty: everyone has their stuff going on and who really needs to hear about mine? 2. feel confused: I generally have firm views of the way forward and somebody else's advice tends to almost derail my resolve, rather than inspire me to do it differently and 3. recognise that I'm not as energised by the conversation as I would be if I just 'had a laugh'. That isn't to say I don't blurt out my inner most thoughts fairly frequently, but I guess I'm not really looking for solutions, more for someone to say, 'That's a nightmare. I feel your pain. Here, have a glass of prosecco with me.'

So I didn’t confide in my friends until I felt better again. But I knew I was not in a good place and that it was foolish to be alone in it.

Rather than simply tell my husband I was down, that the hormones were horrendous and ask him to sympathise, I said that I needed him to help me.  I said that I needed constant reassurance that this wasn't real, that I needed him to force me out of the house, go for my 'power walk' (I knew the importance but you know, sometimes it was raining…) and to make me get enough sleep.  He was brilliant. I think that if I hadn't have asked for help, he would have tried to do the boy-problem-solving-thing which wasn't as effective as giving me a hug and reminding me that we could beat this thing and of the strategy to do it.


The good news is, this situation feels a lifetime ago and yet the operation was less than three months ago. Much of the improvement is due to my hormones calming down (although not so the renewed hot sweats, jeez…) but some is certainly due to having a strategy. I'm lucky that I can now run again and I'm back to normal busy-ness - I'm definitely someone who's better humoured when busy - but I also feel calmer about this new state my body is in because I have faith in the strategies. Combined, they are more powerful than the hormones, so take that menopause, you won't get me that easily.

This is the strategy which worked for me. I'm sure different things work for different people – I'd have thought reading would work for me, for example, I love books and never have enough time to read as much as I'd like, but it didn’t. I couldn’t concentrate – whatever works for you, I really feel that having a plan of attack is your best tool to taking back control.



Jackie Buxton is a writer, editor and teacher of creative writing, living in Yorkshire with her husband and two teenage daughters. Jackie used her recent experience of an aggressive form of breast cancer to inform and dispel some myths about a cancer diagnosis via her popular blog: Agenthood and Submissionville. Her posts became the frame-work of self-help memoire, Tea & Chemo (Urbane Publications, November 2015) which receives heart-warming feedback, and has a five star rating from over 75 reviews. Jackie's recently published first novel, Glass Houses, is about two women's stupid mistakes, the ramifications and the silver linings. Her award-winning short stories can be found in three anthologies, as well as appearing regularly in Chase Magazine. When not writing or reading, over-seeing house and teens, Jackie can be found running, cycling or tripping up though the beautiful Yorkshire countryside.






Links
Blog:                   http://jackiebuxton.blogspot.co.uk


Wednesday 13 July 2016

The End of the Beginning: Dropping the Breast Cancer Bomb ~ Naz ~ HuffPost Blog

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So, you've met someone. You like them. You think they like you. But you have a secret.......

"When IS the right time to drop the breast cancer bomb?.........
For a woman who is encouraged to ‘move on’ a simple track does not exist. It takes time, years more appropriately, to be able to feel what you once did, or the memory of the return. The scars, the limitations, the menopause, tamoxifen side effects, and the agony, that fear of recurrence, that you may, just may, end up inflicting on the innocent ‘other’: is that justified? Yes, it takes two to tango, but what is that they say about love? It is blind, it is dedication, it is commitment: until death do us apart. The end of the beginning."

Read Naz's beautiful and emotional blog post about finding and losing your heart:

Blog published on HuffPostUK, 13th July 2016

Friday 8 July 2016

Panning for Poetry ~ Part II

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The poems that follow have all been written by talented members of the Building Resilience in Breast Cancer Facebook private psychoeducational group.

For this feature, our members were asked to share their own poetry, the feelings and consequent words that flowed and helped them through the storm of their breast cancer diagnosis.

Boob job
I've always fancied a boob job I do have to confess
And now I'm getting one free on the NHS
Do I get the tear shaped or do I get the rounds
I don't really care as long as they make nice little mounds.
So many ones to choose from in the nurse's little folders
And as I'm going smaller I can throw out my boulder holders
It'll be a shame to see them gone but a relief all the same
And hopefully I'll like my new boobs and might even give them a name.
A bilateral mx isn't much to look forward to
But it's my decision and I'm determined to see it through
The lymph nodes will go too but I doubt I'll grieve
But just to be on the safe side I'll be ordering a lymphodema sleeve.
All this talk of perkier tits certainly gets my vote
And I wonder when I'm swimming if they'll help keep me afloat?
So many recon options - the ld, diep and the tram
And with dermal slings and strattices I could even end up smelling of ham.
All this talk of expanders and having them pumped up
I wonder at what point they'll stop so I can see my new sized cup
Of course I worry how I'll feel about the inevitable scars
Just hope the stitching is quite neat then I won't look like I'm from mars.
And bloody rads could spoil my plans for my lovely new companions
So I'm praying that they'll stay convex and not turn into canyons
I'm relieved the surgery date is set and the tumours will be gone - phew
And I think I'll go for stick on nipples so better buy in some superglue!

Written by Colette

~

Bikes and boobs
Can I have a bmx?' I used to ask my mum
'No love, ride your chopper, I'm not made of money hun'
Isn't it ironic if you fast forward 30 years
That bmx's and choppers would be causing me some tears

The surgeon with her chopper has taken away my boobs
Well what an op that was and boy did it feature tubes
With seven sticking out of me, I didn't feel too great
Nor sharing with a woman whose snoring made the ward vibrate

So my old, bad boobs have gone and there are new ones in their place
And looking at the scars was something I wasn't sure I could face
But I've had a good nosey round and they look alright to me
They're quite a perky pair even if they wouldn't make page three

Kids are so amazing and will tell you as it is
'Can I see your new boobs Mummy?', my 6 year old did quiz
So I braced myself and showed him - 'what do you think?, I said
'They're so much better Mummy, cos your others were bigger than your head'.

Written by Colette

~
Reflections
I look in the mirror, and what do I see?
I see cancer staring back at me.
I used to see hair, I used to see a face,
now a disease has taken their place.
A constant reminder of what I’ve been through,
I only see one boob, I used to see two.
I’m hopeful that one day I will forget,
but that day isn’t here, not today, not yet.
But when that time comes, and I am set free,
I will look in the mirror
and see
only me.

Written by Caroline

~


b, c
The diary entry
for June 20th 2011
reads ‘Hosp – 3.20’
then ‘lump, day 1’;
b was breast,
c was cancer,
life was upended.

The diary entry
for June 20th 2012
reads ‘1 year’;
b is bee (small with ginger rump),
c is campanula (poscharskyana),
in whose purple blooms
the bee is upended;
and this is life.

Written by Samantha

~

Turn on the Taps
There are no tears
My eyes are dry.
Sometimes I wish I could just cry,
And mourn the loss of things held dear
Instead of holding onto fear,
Of cancer coming back again
In my spine or in my brain.
I should be happy, so they say
The cancer’s gone – hip hip hooray!
But just for once,
Just for today,
I long for tears to wash away
The shame, the guilt, the hurt, the pain
That cancer causes
Again and again.

Written by Caroline

~

Tamoxifen
Tamoxifen
My new best friend,
those sleepless nights that never end.
Depression, hot flushes and the rest
the side effects are not the best.
And yet I take it every day
to make the cancer stay away
because if it comes back instead
I fear the next time I’ll be dead

Written by Caroline

~

Pentameter
A poet may spend years trying to write
the perfect line of iambic poetry;
turns out my oncologist has the best
'As far as we can tell, you're cancer-free.'

© Samantha Newbury, 20 March 2012

~