Monthly Archives: February 2011

Asking for help is a good thing

27 Feb

A large box full of goodies has arrived on my doorstep. They are frozen meals from a company that claims to be ‘just like homemade’, which is good because at the moment a little homemade comfort is exactly what the doctor ordered.

Radiotherapy is nearly through, I can see the light at the end of the tunnel. Unfortunately, I’m also beginning to feel some of the side effects like tiredness and wheezy chest. Neither of these things are terrible, but they slow me down. And with my husband currently in the last weeks of his thesis writing (he is glued to his computer with papers scattered all around) it would be too much to ask him for a homemade dinner. Besides, the man is incredible but he cannot cook.

So what do you do when there’s no one to cook, clean, and bring you tea in bed?

[Zsolt can bring tea – he’s good at that. But not everyone has a tea buddy for that bit of comfort.]

I guess there are three things you can do.

One: Do things yourself. This has some benefits like pushing yourself, but I think the drawbacks can potentially outweigh the whole ‘in it to win it’ idea. Back during chemotherapy days I wasn’t against pushing. It was because of pushing that I managed to re-train my legs how to walk after those AC treatments, and it was because of pushing that I was able to attend my book club and writing group. It’s good to push. However the pressure did inevitably build into a wee little break down of spirits. Even if you’re the toughest, strongest, most determined cancer-fighter who ever existed, there will come a time when ‘on your own’ isn’t good enough. That’s when a cup of tea in bed, brewed and delivered by someone who cares, is really the best medicine.

Two: Buy some help. This option only applies if you can afford to buy some help. Today I received six premade meals and three side dishes. My husband and I are not rich (we’re rich with love, but the banks at present won’t accept that as credit). However, with him finishing the last treads of his thesis and me finishing the last stage of radiotherapy, we decided that spending a bit extra on meals that are healthy, premade, and actually quite tasty (a rarity in frozen foods), was worth the extra pennies. Now if I could only convince him that a housecleaner would work wonders  . . . but I think that’s a splurge too far.

Three: Ask for help. It’s funny because while this option brings the most incredible results, it’s hard to ask for help.  What’s your general response when someone asks: ‘How are you?’

You: ‘Fine, thanks. How are you?’

Them: ‘Great.’

You: ‘Good.’

Them: ‘Great.’

And everyone goes on with their business. It is generally expected that we suck up our problems rather than pass them on to others. When people started hearing I was diagnoses with breast cancer, they would ask me, “do you need any help?” but that was before chemotherapy had begun. So, by the time chemo actually started, the moment for helpful offers had already passed. It was difficult to contact people (Quick aside: Zsolt’s family are all in Hugary, my family are all in Canada – we are on our own in England while Zsolt pursues his PhD, and while I get treated for breast cancer.) . . . it was difficult to contact people and say, “Please make me food, because I can’t handle this.” Asking for help can be hard.

Which is a shame, because once I became so desperate that I finally asked for help, the results were amazing. People want to help. Organizations are created to help. Charities are run so that we can find HELP. But sometimes we need other people to start the ball rolling, to ask us, “How you doing?” and probe further for a real, honest answer.

I am 100% thankful to all the people who helped me through chemotherapy. And I’m 100% thankful that I’ve learned to get help before a breakdown erupts. Today I felt ill at work but didn’t work on. Instead I came home and got into bed. Cancer taught me that. This week I’m feeling tired, but didn’t keep that to myself. I’ve warned my husband of the change and we ordered meals for the week. Cancer taught me that too. Zsolt knows to come into the room if I’m unwell and ask how I’m doing, maybe bring me a drink. Cancer taught him that.

When this is all over I’d like to give back. There are people out there who need to be asked more often, ‘how are you doing?’ and ‘do you need help?’ There are people who don’t have others who can offer their services (or at least, they think they don’t). There are people out there who I now understand a whole better, a WHOLE lot better, for having been in the same situation. I get the pride. I get the exhaustion. I get the reluctance to raise and hand and say, ‘help me’.

Anyhow. Two more months in England, then three in Hungary to relax and rehabilitate with Zsolt’s family. After that it will be back to Canada, meaning it’ll be a good time to look up ‘meals on wheels’ or a similar organization and start passing forward what others have so kindly given to me: support, attention, healthy meals,  and a cup of tea when most needed.

To read posts-as-they-happen, plus the start of my breast cancer journey, visit me at www.bumpyboobs.com and check me out on twitter.

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Facing the fear of recurrence

18 Feb

Quick catch up: Over the past 2 months I had been feeling some changes in my left (remaining) breast, and they were getting me worried – like, extremely worried. I’d sit up crying as my husband tried to reassure me this was nothing, and no amount of logic could settle my mind that the cancer hadn’t returned, despite chemo only finishing about 1.5 months ago.

And yet – can you believe it – I felt too embarrassed to arrange an ultra sound. Suddenly I’d become one of those patients who run to the hospital for every tiny bump, lump, or change, and that embarrassed me. But you know what, I was being stupid. If you get cancer, you ought to be entitled to proactivey (perhaps sometimes verging on paranoia). So finally, after my third night-time breakdown, I went to speak with my doctors. Here is what happened:

On Monday I went to my GP and asked her to refer me to the hospital. Apparently this was an unnecessary step – I could have contacted a breast case nurse at the hospital directly, but it was good to catch up with Dr Kind (plus I needed to refill my prescription).

Tuesday morning I had a call from the hospital, “Hello Mrs Brunelle, we’ve got a space for you tomorrow morning. Can you make it?”

Yes, I could make it. This call came just as I was entering my acupuncturist’s office, and not even she could get me to stay relaxed after that point. (There was something she did with my eyebrows that was divine and always knocks me out, but five minutes later I was thinking about that breast exam and getting wound up again.)

Anyhow! It was nerve racking. My body revolted against me later in the day and served up a killer stomach ache, which was subsequently blamed on a leftover Valentine’s day dish of cabbage and pork, but was likely also due to stress.

Wednesday I went to the hospital. They sent me to the clinic that contains all things cancer – this is where the oncologists, surgeons and radiation doctors meet to mingle. Passing us in the waiting room was my surgeon who nodded to Zsolt (I was absorbed by my magazine), and as we were shown into a consultation room my oncologist passed by and waved hello too.

Again the nurse asked me to remove my top and put on the cape. You do not have to put on that terrible cape. Maybe if it takes five minutes to remove your clothing, do what they ask, but so long as you can whip off your shirt – why bother with an ugly, cold, and awkward cape?

Generally we wait about 30 to 45 minutes in those consultation rooms, but this time things were quick. In walked a doctor, a student (baby doctor) and – ugh!the same breast care nurse who was in the room when I was first given my diagnosis. Panic threatened to set in, but then I thought to myself, ‘why would they bring a baby doctor along if they had bad news?’ which was logical. It turned out they couldn’t have given me bad news, because they literally had no idea why I was there. A file had landed on their desk (with most of the contents missing because my original file was lost) and they knew I was worried about lumps. But that was all.

After retelling my breast cancer story, showing off the tidy scar, and having my breast checked by yet another doctor, I was assured this was probably nothing, ‘but we’ll send you for a scan anyhow.’

The breast care nurse was very generous in telling me that my fear was normal. ‘If you didn’t feel this way, then we’d be worried.’ I suspect that isn’t true, but it was kind of her to say.

And one hour later I had my ultrasound.

Fast, no?

Again they shot cold gel onto my chest. Again some slippery rubbery thing glided around my breast. Again it probed the lumps. ‘I can feel the lump you mean,’ said the doctor, ‘but everything looks normal.’

Whew. This was a relief. One – I hadn’t imagined the lump. Two – it wasn’t cancer.

Awesome!

And now I can finally enjoy how much better my body feels. Wednesday afternoon I ran up the stairs at work, and only realized half way through that I was RUNNING. My face has regained colour (blood), and my energy is picking up.

There’s so much to look forward to now; the next six months will be wonderful. Hard in some ways because we’ll leave our home, but amazing in others (travelling, spa-going, resting, hanging with husband, graduation, Zsolt turns THIRTY).  I’m finally free to enjoy, boob bumps and all.

So there you have it! I admire women who get past the fear of recurrence. It’s something that I need to learn. But at least until my next scan I have this release. It feels really good, amazingly good, and I’m thankful.

To read posts-as-they-happen, plus the start of my breast cancer journey, visit me at www.bumpyboobs.com and check me out on twitter.

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Slick pits and facing cancer

14 Feb

When the doctor stuck his fingers in my armpit and announced that I had cancer (he was checking my lymph nodes at the time, and all I could think of was, ‘my God, my armpit is sweaty – why am I so sweaty? Do I smell? Gross!) my life came to a screeching halt. Who cared about slick pits? I had breast cancer.

Breast cancer. At twenty seven years old. What the puck?

And for a while,  before I revealed the truth to family and friends, blogging was my support group.  Which is why I’m here today with you at facingcancer.ca (facing cancer and everthing else) because sharing is an incredible help in our journey. Sometimes, you need to reach out to those who empathise. Don’t you think?

Forums, blogs, tweets, Facebook and internet searches are my lifeline: Midnight reaction to medication? Google it! Sex drive reduced to nothing? Forum search! Lonely for a chat? Skype home!

Kicking cancer-ass 21st century style. It’s really incredible.

Like the tag lines says, ‘for everything else you’re going through with cancer’ (because we all know it rocks our world beyond just lump-in-tissue management) this blog is about life with cancer, life after cancer, and life away from cancer.

My name is Catherine. I’ve had one breast removed. My hair is gone. Chemo is finally over, and radiotherapy is half way through. Life is coming back to normal – but I’m taking a step further. Because normal obviously wasn’t working for me. This year, 2011, will be about change and growth and pushing boundaries.

Please join me for the adventure. I’ll keep you posted and would, of course, love to hear how you’re doing. Wherever you are in your journey that load becomes lighter when shared, so don’t be shy.

Bye for now – actual life-as-it-happens posts soon to come!

Catherine Brunelle is an aspiring writing who clings to her passion during hard times. To read about her craptacular adventures in cancer land, check out her blog at www.bumpyboobs.com (promised to be light, fun, and descriptive. Plus, I draw pictures!).

Posted in Uncategorized, breast cancer, chemotherapy, facingcancer.ca, life after cancer, radiotherapy | Tagged , , , | Leave a comment

Forget the pies: Five years later, identity crisis resolved.

12 Feb

You know what? For the past five years – ever since meeting my Hungarian husband and flying away from the country I love – for the past five years, I’ve been asking this difficult question: where do I belong? And it would keep me up at night. Honestly, I’d be awake trying to reason whether we should move somewhere in Europe, stay in the UK, go back to Canada, hijack things to Australia . . . when you’re in an international relationship, the concept of home and belonging are suddenly challenged. Growing up, I had no idea how much Ottawa was a part of my identity – and when taken away, there was this lingering question: Where do I belong?

This mini crisis peaked with the event of our wedding, one moment planned for Europe, the next moved to Canada . . . and still nothing was resolved in terms of the future. Zsolt and I had a dream: house, family, kids, day-to-day happiness and settlement. We wanted to settle. But where? I  began to imagine myself behind a wooden counter in a kitchen, with a red and white chequered apron tied around my waist and a hot pie cooling on the window ledge, which looked out over a lovely green yard with tall, solid trees – and everything would be just right. From the tidiness, to the location, to our lives. Everything, one day, would be just right . . . eventually . . .

And then I got cancer.

Which isn’t to say the dream of a clean kitchen disappeared. I still dream of a clean kitchen. And it isn’t to say the crisis of ‘where to live’ was resolved. Because we’re moving to Canada, but will we stay there forever – who knows?

However, getting cancer (surviving cancer) did change an essential aspect of my life.  I stopped asking: “Where do I belong?”

It suddenly felt like a stupid question.

Where do I belong? Duh. I belong right here – right now – in this moment. And what do I belong to? I belong to my passions, my writing, my Love, and myself.

It’s like a light was flipped on. In the past five years I’ve been hunting for my identity. It was challenged when I left Canada. It was challenged when I was married. It was challenged when I got cancer.

And so it was sharpened.

I am Catherine. I am a writer. I am a wife. I am a breast cancer survivor. And those are things that have no passport, no national identity, no alien status, and no dependence to anything beyond myself (and Zsolt, in terms of marriage). Where do I belong? Geez Louise, I belong within myself. Geography is a luxury, to be close to family a bonus, to have spectacular views, clean kitchens, pies on the windowsill – that’s all wonderful and welcome. But in this moment I’ve got my essentials. I’m where I belong, finally.

All right, today’s blog post is totally inwards, and so sorry for spilling this self-reflection all over the page. But it’s a good revelation, and nothing but experience could have brought me to this point. I suppose as things change, my identity will keep shifting and shaping, but at least right now, age 28, tipping over into 29 and feeling good, I’ve found myself. I’ve found my passion (writing, creating, doing). I’ve found the love of my life. And it all feels amazing.

Happy Easter!

PS. I might have found a sense of identity – but my apartment is still a mess! The other night – in the pitch black and total silence, there was a huge CRACK (I started screaming even before waking up from the shock of the noise and Zsolt had to settle me down). Turns out, my wardrobe collapsed onto the ground. Now there’s a pile of clothes tangled with hangers and shelving on the floor. What a way to get the moving purge started. I’ll need to pick through my clothes/tidy this mess and decide: Canada (to live), Hungary (to vacation), charity (to give me an excuse for more shopping). So, with a push from providence, the packing has begun!

To read posts-as-they-happen, plus the start of my breast cancer journey, visit me at www.bumpyboobs.com and check me out on twitter.

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Easter musings and fertility after chemo

10 Feb

Monday morning. Have spilled orange juice all over myself, but thanks to a damp sponge and a (once) clean tea towel, have cleaned up mess. Weather: cloudy. Apartment: messy. Allergies: active. Temperament: A-okay, despite the orange flavour to my bathrobe.

I nearly forgot that Easter was coming. This year we’re staying at home – going nowhere—for the sake of Zsolt’s study habits and the impending viva.  But I will miss having an Easter with family. In Canada we go to my grandmother’s home (Bonjour Lulu!), or someone’s home in Quebec, and share a lunch. My family is comprised of cooks and bakers, and people generally produce excellent food. Like, lick your fingers and smack those lips excellent.  When we were younger (proper grandchildren rather than adult grandchildren) Lulu would always hand out these large chocolate bunnies with marshmallow filling. They were pretty to look at – I loved the idea of them, the idea of the chocolate and the bright pinks, yellows, blues on the wrapper . . .of a bunny who collects painted eggs and carries a blue tinfoil basket. . .  but could never bring myself to love the idea of marshmallow filling.

In Hungary, Zsolt’s mother will hard boil about two dozen eggs, and his sister will prepare the dyes out in the garden. Then we’ll sit around for an hour or two and dye the eggs. I love it. After you have your egg dyed with whatever colour arrangement you choose (all red, half red, half blue, some purple in between, or yellow and blue with a green band, etc) you take some pork fat and rub into the egg shell to make it shine. On Easter morning people crack into the coloured eggs, but Zsolt’s mom saves the prettiest ones from hungary fingers.

And speaking of eggs, I have a fertility appointment this week. Wednesday.  It’ll be a family gathering of sorts, in that it’s about family and there will be a gathering – just not of the Easter kind.  A good friend recommended I stop thinking about fertility and just give my body a break. Sound reasoning. It’s on my ‘to do’ list (along with some meditation). But first there’s this appointment.

People tell me that I have options. Okay, Catherine, you have options. The doctor last week very kindly told me that ‘it’s highly likely you’re period will come back’. It’s nice when the term ‘highly likely’ refers to something good.

There is this option of egg donation. Have you heard of it? Essentially, a woman donates an egg, and the recipient of the egg can have it inseminated with a man’s sperm (her husband’s or partner’s I assume), and that egg is then planted into the recipient’s womb. I guess it’s a bit like in vitro fertilization. And that’s where my knowledge stops. Are the chances of conception similar to in vitro? Would I need to take a load of drugs beforehand? Are women truly willing to give up their eggs?

Zsolt said, ‘well women lose an egg every month if they don’t conceive’, which is true. But for some reason, it feels entirely odd to imagine donating eggs. It feels slightly like donating a baby. But men have done this for ages – they have sperm banks for goodness sake, and I’m not sure they feel similar inhibition to the idea. Maybe that’s because it’s a generally accepted action for men (“go forth and procreate”)? Or maybe it’s because the process is far more invasive for women? I don’t know. If you had asked me two years ago if I’d like to donate some eggs to women who cannot conceive, there is a good chance I would have passed. But now, waiting for my period to return with crossed fingers, I’m starting to realize a different perspective.

Then there is the adoption option. Another murky area. The idea is very nice, and almost ideal if you cannot have children. Plus, you’re making a huge difference to a child’s life. Surprisingly – but of course, if you really consider it – a social worker friend told me that most babies/young children adopted are those removed from their families because the parents are deemed unfit. Of course, this doesn’t change the fact that adopting one of these children would be a blessing, but you can see how there are complications.

And then I guess there’s ovary stimulation? I really know nothing about this. For all I know, the doctor takes a giant feather and tickles a woman’s belly. But I’m guessing it involves hormones and drugs and all those little goodies I’d rather avoid.

Anyhow, Easter is coming, and I have trouble not thinking about my lack of menstrual cycle. All these baby chicks and lambs and horses – all my friends totting their beautiful children – it makes me wonder, will I be part of this?

Before cancer the answer was, ‘yes’.

After cancer (after chemo) the answer is, ‘hopefully’.

Right, back to Monday morning. Orange juice is under control. Time to make some breakfast if I can find a clean dish in this mess. Yesterday I made a fantastic meal of some curry chicken and soup. But fantastic meals leave me knackered, and I can never bother with the dishes immediately. As a result my flat looks like a culinary Armageddon.

But that’s okay.  And now, onwards with the day.

To read posts-as-they-happen, plus the start of my breast cancer journey, visit me at www.bumpyboobs.com and check me out on twitter.

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Itsy bitsy, teeny weenie, scar disguising string bikini

8 Feb

Yes! Punch in the air! Cross off my first vacation of the summer. It’s been about two years since Zsolt and I travelled (apart from trips home, but that’s more comfort than adventure), so landing those excellent tickets to Faro was a real treat. This trip became, essentially, a confirmation of my recovery. Proof positive that chemo can’t keep you down forever.

Mind you, it’s easier to say this on the completed side of chemotherapy. I can remember sitting in those hospital chairs (drip, drip, drip) and dreaming about the summer. In the summer, I told myself, everything would be okay. I’d be free of drugs, free of exhaustion, and free of cancer. But as the Benadryl took hold and my head became groggy – well, life without cancer felt like a far away dream.

But this week I flew to Portugal. This week, I travelled again. Before my cancer diagnosis Zsolt and I had planned on a round the world trip. That was quietly shelved when the big C was pushed into our lives, but my wanderlust never settled. One of the reasons I kept returning to the hospital was so I could eventually leave it to never return again, totally sans cancer – and my carrot at the end of that stick was the dream of vacation.

Of course everyone recovers at their own pace. The doctors were quite clear that the chemo would leave me tired for at least six months after the last treatment. So I think I’ve been quite lucky. While touring around Lagos my husband and I decided to do the cliff walk. Apart from the wayyyy too steep, wayyyy too unguarded trails, I  was fine walking up and down these cliffs along the beach. Flashback five months ago: I couldn’t manage steep inclines, stairs winded me, and forget about long walks by the seafront (if Southampton had a seafront, which it doesn’t).

Things have gotten better. Much better.

And I was able to wear my cute summer clothes, too.

Totting a badeau bikini I even went sans prosthesis to the beaches. Really, my chest is so flat anyhow it’s hard to notice the absence of a second breast. Plus, my bathing suit has a busy pattern, which helps disguise the difference.

Add on my short hair, and I looked rather cute out there on the sand. I’d like to think people assumed my hair was short due to cutting edge style choices, and not because of chemotherapy. We as cancer patients might assume people know our diagnosis, but I can remember the days when seeing a woman with short hair didn’t make me assume she was a survivor.

And in the mornings we would tour the old town, then pick up some pizza (gluten alert!) and fruit, head to the beach, and then eventually return to the guest house. We stayed in this lovely place outside of the city centre – it was about a fifteen minute walk, but worthwhile due to the kindness of the owners, the cleanliness of the rooms (five stars for cleanliness) and utilities provided. Plus, everyone who stayed at the guest house was really easygoing. I had forgotten how enjoyable the company of other travellers can be. When people are on vacation, they’re generally pretty cool. In fact, we even met a lovely Hungarian couple – honestly, for such a small country the Hungarians seem to be everywhere. I haven’t gone on a trip yet without hearing Hungarian at some point. [FYI my husband is Hungarian]. We cornered this couple in the kitchen and essentially twisted their arm to play a card game with us (Zsírozás) – Zsolt was the reigning champion, but Dávid was quite a competitor. Meanwhile Hajni and I did our best, but seemed to get trumped every round. And I ate ice cream the entire time.

I guess what I am saying through all these holiday rambles is that my life is – at this moment – exactly as it dreamed it could be. In an interview on television about Look Good Feel Better and Facingcancer.ca, Sherry Abbott mentioned that women “grieve their lives as they once knew it,” which is absolutely the truth. But I’ve got to say, during these past few months I’ve started to accept this next stage of life: Catherine after cancer, and she looks pretty darn good in her skimpy bikini. No doubt there are scars, but I’m learning to move on. Reaching this goal has been incredibly relieving. I’d like to wish courage and speed to anyone sitting in a chemo chair (drip, drip, drip) and dreaming of the better things to come.

They’re coming, all right. Just hang in there. Good things are on the way.

And speaking of travelling: Shout out to Terri from afreshchapter who also blogs for facingcancer.ca, and has just started her adventure in South Africa. Yet another example of great things laying ahead. Boy, do I have travel envy.

To read posts-as-they-happen, plus the start of my breast cancer journey, visit me at www.bumpyboobs.com and check me out on twitter.

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Buying travel insurance after cancer

6 Feb

As you may (or may not) know, Zsolt and I have decided to get away. Where to? Portugal. Not for long, just a short break – the Ryan Air ticket was so inexpensive that we jumped on the opportunity for a reasonably priced vacation. I’ve heard rumour that the weather is above 20 degrees and sunny (drool) in Faro, which means for the next few days I’ll be sprawled across a beach towel and soaking the vitamin D.

Anyhow, jump back to last night. What’s an essential when travelling abroad? Finger on nose if you’ve guessed it: travel insurance is essential.

When comparing prices we generally go to moneysupermarket.com. I’m not positive they’re the best, but their advertising is hilarious – good marketing wins again. With their search engine narrowed to ‘travel insurance’, the enter button is pushed and a long list of options appear on the screen.  Hmm, cheap.

The EU has this scheme established where you can go into another EU member country and have access to their medical assistance in an emergency. There are limitations, but in general if you fall and scrape your knee – and  you’re an EU resident – you won’t need to pay 100$ for a bandage. However, what is covered varies country to  country, which is why buying travel insurance is smart.

Which takes me back to moneysupermarket.com  – £6 for two person coverage sounded almost too good to be true. And guess what? It was.  Okay okay, for £6 (about 9.50 Canadian bucks) you cannot expect too much from an insurer. . . but I wasn’t  quite ready for the shut down they delivered.

Looking over the policies and conditions I ‘CNTRL+F’ed  (aka searched) “cancer” and found nothing. Then I ‘CNTRL+F’ed “illness” and found lots. Essentially most insures state they won’t cover any medical costs arising from an existing illness. Fair enough. It’s not as though my boob(s) are about to explode, so no worries on my end about the existing illness.

Onwards. Click “purchase” and proceed to the next screen.

This is where the brick wall showed up. Essentially, the medical screening consists of a question along the lines of “have you or anyone being covered by this insurance have or ever had any of the following,” and of course – of course, there was cancer. It’s not like they cared what type of cancer, or whether it’s gone, or in recession, or appeared once and then disappeared forever . . .they don’t care. It’s just: tick this box if you’ve ever had it.

So I ticked the box.

And of course was denied insurance.

Anyhow. I became a steaming kettle of indignation. Like I said, my breasts are not going to explode because last year I had cancer. Right, my lymph nodes are gone – so maybe there is a risk of lympodemia . . . but the question didn’t ask about lymphodemia, it asked about cancer.

Grumble grumble.

That’s when I gave up on the hunt for cheap insurance and went digging through my breast cancer information. There is a UK company called ‘insurepink’  who cover those diagnosed with non-terminal cancers (specifically aimed at breast cancer) – it was still more expensive than what moneysupermarket.com offered, but I suppose that’s to account for my pre-existing medical condition. If anyone knows of a Canadian equivalent to this, please do post it in the comment section or send me a direct message. I’d love to know.

Even on this site I had to answer about 25 questions about my condition, but at least they bothered to ask the specifics rather than apply a blanket policy of exclusion.

Funny . . . imagine being cancer-free for over 35 years, and you still need to tick that little box. Even when cancer is gone, it’s not totally gone.

So that was an interesting experience. Thank goodness for Insurepink. Righto – on a brighter note, time to fly away to warmer places. No more cancer thoughts for the rest of the week. Have a lovely start of April. See you soon.

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How cancer hijacked my writing

4 Feb

Good Monday to you! Whew, what a weekend. Totally exhausting. This past weekend I attended a local writer’s workshop. It was exciting to be in a room with other writers – felt a little like camp, with the musty building smell contributing toward that atmosphere, and we’re all there to play games, learn about our writing and take home priceless memories (aka tips on finding an agent). And the opportunity to meet and chat was really helpful. In some ways it was like getting together at the Look Good Feel Better seminar [see blog from last week], in that we were there for ourselves, but ultimately ended up supporting one another.

I think whether you are a cancer-survivor, writer, artist, homemaker, whatever . . . being in touch with like minds is essential. They’re the people who ‘get’ your crazy. Whether it’s worrying about reoccurrence or family life or whether the storyline works . . . being able to connect with those who understand is such a great support. Don’t you think?

So we were asked a question during this workshop: why do you write? And I thought about it  – about the project I’d been working on (not my blog, but my fiction) before the breast cancer diagnosis, which is the same project I’m coming back to now. Why, Catherine, are you writing this?

And the answer was interesting, so deeply emotional, that it nearly blew me away.

You see, I’m writing a novel (who isn’t!) that is about nine generations of women across nine months of pregnancy. Each month of pregnancy is a snap shot from one women’s life.

Originally I began to write this story because I had wanted to get pregnant. I had wanted (autumn 2010) to start trying for a baby. That was the plan between Zsolt and I, which frankly left me feeling nervous as heck. So, what to do when nervous and uncertain? Write it out. And I began this lovely story. It was like I could pull on the strength of previous women who have all been there and conquered that – and that would make everything okay once it was finally my turn. Anyhow. Why did I write it? Because it was a coping process. I was getting ready.

But then cancer happened. Chemotherapy happened. Worries of reoccurrence happened. And now I can’t have children for at least two more years, and that’s assuming my ovulation resumes – and so far, no clear signs indicate that having happened. Giving birth has become a question mark, but not becoming a mother. One way or another, I’ll become a mother eventually.

So . . . nine months later (according to my blog archive of entries) and here is the question again: Why do you write? Or better yet, Catherine, now that you’re not planning to get pregnant any time soon, why return to this story?

Here is the answer I found this past weekend: I’m writing to heal.

In a way, the women of my story are like children. I created them, and I need to take responsibility for their journey. The uncertainties of pre-cancer are still there and they still need to be addressed. But cancer or no cancer, I’m a mother to my narrative. And once day, I’ll be a mother in real life too.

Anyhow, there you go. That’s a snapshot of my life away from the big C – which funnily enough, is still effected by this past year. There’s no escaping what has happened, but at least I have my writing to see me through.

To read posts-as-they-happen, plus the start of my breast cancer journey, visit me at www.bumpyboobs.com and check me out on twitter.

Posted in facingcancer.ca, finding support, life after cancer | Tagged , , , | 3 Comments