Tag: breast cancer

A Picture of Denial.

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I spoke to a friend the other day. A friend who was deeply upset, because one of his friends had left it too late to check himself out… and now has a cancer which can’t be cured. We don’t yet know how long he has. It’s heartbreaking, and more so because it could have been avoided.

In the meantime, I’ve been receiving – for two bloody years – requests to put a heart on my wall, or an eight ball as my status, or to accept the challenge of posting a black and white picture, or a no make-up selfie, to raise awareness for cancer. Well, challenge accepted. Here’s my black and white, no make-up selfie, no hair selfie, no boob selfie, and no husband selfie. Our most recent portrait together, a few weeks ahead of our fifteenth wedding anniversary. ❤️

You don’t raise awareness of cancer by putting little gimmicks on Facebook. You raise awareness of cancer by sharing links to websites which outline the signs of cancer, like this one. You raise awareness by talking about cancer, and not being frightened to tell your doctor, or your friend, or you partner, that you’ve got a lump in your boob or bollock, or that you’re pooing blood, or that you’re struggling to swallow. The earlier you catch a cancer, the easier it is to treat. It’s not going to stop growing just because you don’t want it to be there, but it might not kill you if you do something about it early enough. And guess what? The process of my husband’s death was far more undignified than any check-up or operation, and had we caught his cancer earlier, he would still be here now – healthy, happy, and bringing up his children.

I’ve had more people pummelling my boobs over the last few months than I’d ever thought would be appropriate only weeks after being widowed, but it’s been worth it, because our little boys won’t have to watch another parent die. My left breast is now dangling in formaldehyde in a lab somewhere, probably. My hair is in landfill. And my husband is ashes, in a box. We miss him every second of every day.

I hate the way I look at the moment, but I hate the way my husband looks more. He’s going to look like that for far longer than I’ll look like this. Anyway, he was always keen to make a point at any cost, so maybe, together, at our least glamorous, we could save a life.

What are you most frightened of? Looking like me? Or looking like him?

See your doctor if you’re worried. This is what denial looks like.

Love Fanny x

Fanny’s Family Portrait 2017

Chemotherapy: The Highlights.

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As I come to the end of my final cycle of chemo for breast cancer, and as the side-effects gradually start to wear off, I’d like to reflect on my personal highlights. If you’ve been there, feel free to add your own in the comments… 

1. It’s a bit like being pregnant. You’ll spend at least three months of your life feeling nauseous, with a hospital bag packed and ready, and you’ll have to treat soft cheese and shellfish with the same contempt as nuclear waste. And your tits will never be the same again.

2. Baldness can be liberating. At first. As even more hair falls out, the time you save not having to do your hair will be spent attempting to draw on ever more complicated eyebrows. You’ll save a fortune in waxing, though, so – every cloud.

3. But… as a cancer patient, you’ll qualify for a Look Good Feel Better course. A makeup lesson, complete with free bag of makeup in someone else’s colours, in which an unfeasibly elderly Michelle teaches a roomful of baldies how to contour their faces back out of The Chemo Swell and more towards normality. An extra tutorial on blending into the non-existent hairline might have been handy.

4. You probably won’t lose weight. In fact, the combination of anti-nausea drugs and steriods may make you pile it on, and apparently the one lost boob and a whole head of hair weighed nothing. Fucking NOTHING. I added a stone in 18 weeks. The pre-treatment weigh-in is a reverse Slimming World in which the nurses congratulate you for gaining a few pounds, and you have to smile and try to hide the fact that if you’d known about The Chemo Stone you’d never have agreed to having the bastard stuff in the first place. ( Obviously that’s a lie. You graciously and gratefully take whatever drugs might make you better. But you still feel shit about piling on the weight.)

5. It’s not all dreadful. Towards the end of each cycle, you may feel quite well. While there are many, many days ranging from feeling very ill to mildly off-colour, for much of the time, you can live your life. I worked daily (from home, admittedly,) still took the boys to their sports games even if I couldn’t always watch, and walked the dog on non-shit days. In fact, the more you do, the less time you have to think about how awful it is, and there’s no need to think like an ill person. Being widowed on chemo has been the toughest thing I’ve ever done, but actually, in hindsight, I’m proud of myself for not crumbling. I couldn’t afford to. I’m also truly grateful to friends and family for stepping in on the occasions when I’ve been stuck.

6. Talking of which, you’ll definitely find out who your friends are. And who your friends aren’t. ‘Nuff said.

7. Wigs. Itchy little fuckers. I didn’t usually bother. You’ll only need to find out once though, the hard way, that it’s a good idea to keep an Emergency Hat by the front door for that unexpected visit from the postman.

8. Chemo Brain. It’s an actual thing. I had a point to make about this. Forgotten what it was.

9. Needles. You’ll get used to being cannulated all over, but the daily self-injections are prickly little bastards that boost your blood cells, and you have to do those all by yourself. Take a deep breath, lift your dress, shove it in, and breathe out again. Similar to, but much less fun than, mediocre sex.

10. Loss of taste. Tabasco on EVERYTHING. You’ll know you’re officially ill when you go off alcohol.

11. The menopause. Or not. My ovaries decided to have a ten week long bloody protest in desperation, but have given up for good in favour of hot flushes. Keep a leaflet with you at all times as a makeshift fan (in my case, I use the order of service from my husband’s funeral which has never left my handbag. I like to think he’s doing his bit to help.)

12. Constipation. Or diarrhoea. Or both. Either way, when you finally produce a firm, slippery, satisfying turd you’ll never have been more pleased with yourself.

13. Every fucker’s an oncologist. Smile politely as perfect strangers trot out all the miracle cures they’ve read about on the internet. Or share their own cancer stories. My personal favourite amateur surgeon is a chap I meet on my dog walks. He’d noticed I’d lost my hair and, because we’re northern, he wasn’t too polite to comment. He told me he’d had radiotherapy ten years ago. “Doesn’t work, you know,” he ventured. Well, mate, I’d like to wager that if you’d had it ten years ago, then it probably actually did.

14. Sympathy central. Cancer is the Rolls-Royce of illness, bringing with it everyone’s sympathy (and free parking at the hospital,) but there are definite degrees of shit, and most people who catch theirs early will almost certainly survive. People with other, more permanent life-limiting conditions – Crohn’s, MS, MND, mental health problems, etc. – don’t tend to get the same cocked-head reaction, yet their condition is ongoing, with no cure so far. If you’re lucky enough to have a treatable cancer, please remember those less fortunate when your hair has grown back and you’ve got your all-clear.

15. Sick bowls, not swords. Walking around with a sick bowl under your chin for a few weeks doesn’t make you a warrior. There are no “survivors” and it isn’t a “battle.” I found a stage three tumour in my breast in enough time to be cured. My husband had a stage three tumour in his oesophagus and died. Did he not tell the doctor in time, or fight hard enough? No. We both turned up to all our appointments and took all available treatment. I was lucky. He wasn’t. For his sake, and our children’s, don’t tell me I’ve been amazing. He was, too.

16. Living is lucky. If you’re fortunate enough to be rid of the bloody thing for good, please don’t let the shadow hang over you forever. Worrying about it won’t change anything. We all diagnose ourselves with an incurable brain tumour the moment we get a headache, but people who’ve had cancer before are more likely to be taken seriously by a doctor if symptoms persist. So, keep an eye on yourself, alert the doctor to any changes, and in the meantime, bugger off and live your life to the full, in honour of those who didn’t make it. They really do want you to.

Love Fanny x

*Bear in mind that all cancers are different and all chemo regimes have different side effects. Many don’t cause hair loss, for example. My treatment regime was Cyclophosphamide and Epirubicin for 9 weeks, and then 9 weeks of Docetaxel/Taxotere. Oh, and a massive overdose of tumour humour.

Picture by Askell on DeviantArt

Warts and All.

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I haven’t buried my husband’s ashes yet. I still can’t bring myself to do it, although there have been some conversations with the vicar, so we’re moving forward, slowly. The other day, our son – who had hitherto been quite reluctant to part with them – asked when his Dad would be buried. I said I wasn’t sure.

“Oh,” he said, with obvious disappointment. “I wanted to go and lay some flowers on his grave for Fathers’ Day.”

Those boys are hurting, badly. And it’s only now that I realise just how much, and how much twelve-year-old boys without a father, or even a father figure, struggle – because I can try to be Mum and Dad, but it’s always going to be a compromise. I’m stretched so thinly that I can’t give them everything they need, and I’m taking a lot of my own stress and anger out on them.

Our boys were lucky. For ten years, they had the very best dad in the world, and I don’t use that term lightly. They really did. Nobody adored their children the way he did. He wasn’t always soft with them, but they were exceptionally close and the boys knew just how much they were loved. I was looking through some family photos last night, and what struck me the most was that the same little boy who asked to lay some flowers on his Daddy’s grave was always – always – pictured nuzzling into his father. Not just standing there. Nuzzling him. They adored each other. Even as his mother, I can’t begin to comprehend that child’s loss.

One thing I’m beginning to notice, now I’m a double – not single – parent, is how jealous and angry the boys are with other children whose father is still alive. They are furious. It isn’t fair. These dads – great as they are – are not my children’s dads. They’re pretty good prototype dads, but our boys’ dad was the real deal. The best in the world. They don’t want their friends’ dads. They want their own. When kids complain about their dads being grumpy old arseholes, my boys are cross about it. But at least you’ve got one, they think. You don’t know how lucky you are, they think. They’ve chosen to forget what a grumpy old arsehole their own dad could be.

It’s easy to look back with rose tinted spectacles, and my two do. Of course they do. They are children, and they think like children, but it surprises me that many adults think that way, too. On the online forums, widows and widowers write with great bitterness about friends who turn to them to complain about their (still very much alive) spouse, expecting their widowed friend to listen with sympathy. They don’t. They listen with rage and regret, because they’d give anything to have their own spouse back. They are angry. Angry with anyone who still has their family.

I don’t feel quite like that. Much as I wish my own family was still complete, I actually love to hear my friends complain about their partners. It’s what we do, we women, and being confided in makes me feel as if I’m still valid as a wife, mother and confidante. That I’m still normal. One of the gang. Men are terminally idiotic, and rolling our eyes at how stupid they are is every woman’s favourite pastime. My husband was no exception. He was grumpy, untidy, and out of shape. He never got around to finishing odd jobs, or picking up his wet towels. Don’t get me started on how keen he was to share his opinions, or what a terrible back seat driver he was. I’ve stopped and thrown the car keys at him in the middle of a busy road and told him to drive the fucking car instead then on more than one occasion. He could be a complete twat at times. But, as a husband, and a father, he was the whole package – from wanker to wonderful – and the only person we wanted to fill those very special roles. He was OUR massive fucking annoying twatbastard, and we wouldn’t have changed him. Well, not completely.

As a grieving widow, I’m so desperate to have him back – warts and all – that it’s actually important to remember that there were warts. Plenty of them. My husband’s greatest fear, before he died, was that he’d be canonised in our minds and remembered as some remarkable and faultless being. I assured him that this would never happen. While I can accept that he had faults, and love him because of them – not in spite of them – our children don’t yet have the emotional intelligence or maturity to take anything other than offence at other children’s comments – both positive and negative – about their own fathers. They miss their own too much.

Since he died – actually, no. Since before he died, when we knew he’d never get better, the boys have begged me to provide them with a new stepdad. This seemed odd to me at first, and actually a little offensive, because I couldn’t understand why they would suddenly want someone to take their beloved father’s place. But, they tell me that they just want to be a foursome again. They hate having to divide me in two, and think that if someone made me happy then I would stop crying all the time. (I also think there’s another rather significant element, in that they could really do with someone else around to offer lifts.) In their imagination, their stepdad is a man just like their Daddy. In reality, if they ever do have a stepdad, he’ll have baggage – probably a few kids that they may or may not get along with – different opinions, and a whole new selection of funny little ways. He won’t love them the way their Daddy loved them, because – by definition – he will not be their Daddy. He will be, just like my husband, unique. Irreplaceable. Different. I’m not sure I’m ready for different. I’m not even ready to accept that there’s a vacancy.

When other women whinge to me about their stupid fucking husbands, it doesn’t bother me at all, partly because I like to remember how often I felt like punching my own, and partly because it reminds me that I really am in no hurry to meet another man. I pity my friends, because they never had the privilege of being married to my husband. (Well, a couple of people did, but we’re not really in touch with them any more.) And I pity anyone who one day thinks they could fill my husband’s shoes. The only thing that hurts me deeply is seeing other couples loved up, and their children behaving, as ours used to do. A few weeks ago, I stood with extended family on a beach – the rest of them cuddling their spouses and adoring their wonderful children – as I screamed at my two to stop twatting each other and drawing massive cocks in the sand. My little family was unravelling in front of my eyes and I’d never felt so alone or missed my husband more.

I don’t want a new one, though. Maybe because I’m approaching the end of my treatment, and beginning to see a new start in life ahead of me which I know my husband would want me to grab with both hands, I do occasionally wonder if it’s time to start thinking about dating – not because I need male attention, or rampant sex, but because I’m beyond knackered and could really do with someone to let the dog out early in the morning every now and again.

I can only imagine the internet profile: Bald, one-titted widow. Mediocre cook. Needs a bit of a hand with the kids. Struggling to put up some shelves.

No thank you. Yes, I’m exhausted. Yes, I’m beginning to realise just how desperately my children need a father figure. Yes, I’m finding being Mum and Dad very, very tough. But I’ve just spent Fathers’ Day with our boys, ignoring the significance of the day, mending some garden equipment and building a new drum kit. I even changed a lightbulb. There was no trip to a grave, because there still isn’t one, but I know that their real dad will have been with me all the way, watching me use the wrong bloody spanner, and desperate to jump in and criticise. But he can’t. And what I wouldn’t give to roll my eyes, throw the spanner at him, and tell him to fucking well get on with it himself then, one more time.

We miss you, Superdad. Warts and all.

Love Fanny x

 

 

Bastard Funeral

Not my husband’s funeral flowers. He’d have approved, though. Image from Pinterest.

 

 

 

 

 

Happy Birthday, Dear Chemo.

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My relentless positivity is waning. The dark thoughts are setting in, and becoming far harder to shake off than the last few eyelashes which have long been sobbed into a snotty tissue. I have two children who miss their father, but I miss him too, and if it weren’t for them, perhaps I wouldn’t have bothered to fight this at all. In fact, I think I resent the fact that I can’t just say fuck it and join him, wherever he is. Because I do have his beloved children, though, and no family nearby to bring them up, I don’t have a choice. But, Christ, it’s hard – especially when the two children you’re doing it for are not helping you to row upstream, but are standing on the riverbank, chucking rocks at you as you try to do it alone.

They’re eleven. Nearly twelve. And they’re about as much fun as you’d imagine a pair of bereaved pre-teen boys dealing with yet more cancer to be. We’ve been talking about their forthcoming birthday celebrations. Supermum here has always made sure they had a party – and a bloody good one. Well, they’re twins, so I massively overcompensated for the fact that they never got to have a party of their own (the obscene quantities of pirate bunting in our loft are testament to that.) But, yet again, this year, the thought of a whole load of boys in the house (all, inevitably, being dickheads – none more so than our elder twin) fills me with fear. And I’m trying to plan the date around my chemotherapy, and find a weekend when I’m most likely to be well enough to cope.
So why not postpone their birthday? Well, because this is the fourth birthday of shit, and they barely remember what life was like before cancer. The boys were eight when our world was turned upside down. On their ninth birthday, I handled things, because their dad was on chemo. He was involved in the party, but not feeling too well. They understood that it needed to be low-key, and that their next birthday would be better. On their tenth birthday, I handled things, because their dad’s first round of palliative chemo had just begun. They had a sleepover, but it was low-key, and they were really good about it, because they knew it might be the last one with their dad. On their eleventh birthday, their dad had just died. They had a sleepover and a trampoline party, but it had to be low-key, and we were all feeling pretty flat but didn’t want to not celebrate, because that’s not what Dad would have wanted. Just widowed, I didn’t have the energy to field a whole houseful of Year 6 boys, but I’d promised them, now that the whole cancer thing was over, their twelfth would be one to celebrate. And now, yet again, one of us is bald, sick, and having to crawl through yet another birthday on our knees.

None of this is fair – not on me, but not on them either. Recently, I’ve begun to identify the problems, and there are so many, I don’t even know where to begin. My husband and I had all the answers, you see. We were the greatest team in the world, and our children were brilliant. Not perfect – still little shits at times – but loved, secure, interesting, engaging, and funny. Happy. Really happy. We were so fucking smug about how happy they were, because we were getting the whole parenthood thing pretty much right. We decided, when they were tiny, that the greatest gift we could give to them was The World, and went on wonderful adventures to faraway lands with two little smiling blond boys, all skater shorts and smiles, who could have stepped straight out of a Boden catalogue. People would stop us in the street and talk to us, wherever we went. Our openness and sense of fun must have shone out of us. I didn’t realise at the time how precious this was, or how far down the spiral of shit we’d all fallen, until I walked into the house the other day to find one twin in his new natural habitat, fingers glued to the X Box controller and half an eye on a YouTube video about Fifa or wanking or whatever, and the other screaming into a kebab because the idiot in the shop had put salad on it. The stupid fucking twat.

They’re awful, gobby and angry, and I’m beginning to understand why. Because, three years ago, I was the same. I hated their dad being ill. I sympathised with him, because I’m an adult and (three weeks out of four, anyway) more rational than a little boy, so we talked about it at night and hugged each other better. We were both fucking furious with the disease, but while he just laid there being ill, I had to run around and pick up the pieces of the life we had before, and it made me bloody angry, but he understood, and he kissed me better. Our entire life as we knew it had been ruined, but I thought if he could just get off the sofa and pretend to be well, or turn up to football matches, or attend parents’ evenings, everything would be OK again. All those feelings of rage within me have now been turned on to me, by our children, who see me being defeated by the same damn disease which claimed their dad. They are afraid – quite legitimately – of becoming orphans. At their age, I’m fairly sure that my greatest concern was which member of New Kids on the Block I’d marry first. (Not Donny.)

Well-meaning people constantly tell our boys to look after me, but it’s the worst thing they could possibly say. It implies that we could all have done more as a family to save their dad, if only we’d looked after him better. It isn’t true, and it hurts so bloody much. We could not have saved him, and the boys can’t save me. We just have to hope that I’ll be fortunate enough to be on the right side of the survival statistics, and I believe I will be. Either way, there’s not much I can do about it, but by the time they really start to believe I’m fine, when this is all a dim and distant memory, their childhoods will be over for good.

In only a few weeks, we’ll be back to normal. It won’t kill the boys to have a bit more screen time until then. It won’t hurt to just eat freezer food with oven chips. It’s fine if they go to bed a bit late, or haven’t brushed their teeth for precisely two minutes. Or at all. It doesn’t matter if they didn’t work all that hard at school today. Only a little while to go, and we can pick up again where we left off. Never mind that they don’t want to do drama at the moment, or cricket, or roller skating, or football. It’s fine. We’ll go back to it in a few weeks. It won’t permanently damage them if they don’t eat their vegetables for a while. Just let’s get through this bit of chemo and then we’ll slide back into normality again.

We’ve been saying all that for their last four birthdays. This brief hump of chemo, to overcome in whichever way we can – and another, and another – has become a lifestyle. An entire childhood. Because I don’t have the energy to pick many battles, I’m letting a lot of things slide. In fact, half the time, I’m lying down and crying while the pre-teen cavalry ride roughshod over me with their Xbox controllers and tracksuits, grunting into their phones, and dropping bits of unwanted kebab salad in my ear.

We’d always been honest with our children about cancer, from day one. They knew their Dad’s would be a tough one to fight, respected our honesty, and believed us. We shared our triumphs and our darkest moments, and realised that no amount of stretching the truth would stretch out his life, so saving their feelings with white lies was pointless. As the oncologist said, if a miracle happened, the boys weren’t going to come back and punch him in the face for making their Daddy better. However, the doctors made a mistake. They thought he was getting better, and we told the boys we’d still be a family for a year or more. We hugged each other with delight, and booked another holiday. Six weeks later, he sat on our sofa late on a Friday night, having been brought home in an ambulance, hooked up to an oxygen tank and permanently discharged from hospital. We hugged and cried with our beloved boys again, as he told them they’d missed the biggest tumour of them all. It wasn’t fluid on his lung. He had been brought home to die. And guess what? Our boys now don’t believe anything that the cancer doctors say. So, why would they believe that I’ll be alive for their thirteenth birthday, even though the doctors are sure that I will be? Why would they trust that we’ll ever go on a Christmas adventure holiday again, when the last three have been cancelled?

And nobody really, truly understands. Even I don’t understand. That’s why, maybe, despite my kids being the most difficult, angry, stubborn, malnourished, over-screentimed, worst people in the world at the moment, I still feel the need to fight their corner. I observe the boys and their friends a lot, and canvass opinion with other parents, and the general consensus is that they’re no worse than anyone else’s children at this stage in their lives. In fact, considering what they’ve been through, they’re doing bloody well. They’re working hard(ish) at school, seem popular with teachers (mainly,) are maintaining and developing friendships, and are also going through all the usual shit of being picked on or dropped by others. But that’s what kids do, and – for the most part – I let them get on with it, because two oversensitive kids who are already struggling with friendships probably don’t want some bald-headed titless wonder wading in and cramping their style. Apparently, some of their friends are bored with hearing about cancer now. Well, so the fuck are we.

In a few weeks, when the chemotherapy and radiotherapy are over with, I like to think we will – somehow – find this elusive New Normal. The one we’ve been trying to find for so long. The one with discipline and energy and fun and good manners. And possibly even one or two vegetables. (Sadly, I think I’ve probably lost the Battle of Boden, and the tracksuits are here to stay for the foreseeable future.) Until then, I know I have to just keep a lid on it and understand things from our children’s point of view, when I’ve stopped screaming at them. Our children, who still play football on a team run by dads, who desperately miss their own dad being on the sidelines, cheering them on. Our children, whose mum had no sooner taken the role of Dad, than she’d begun to disappear from the football sidelines as well. They don’t believe it’s temporary. They don’t believe I’ll be back, willing them to victory next season, along with their friends. I intend to prove them wrong.

Until then, I’m going to give them the one thing that their friends have had every year, even though our boys probably don’t deserve it – a birthday party, with cake and candles, friends and fun. And, next year, there will be no cloud of doubt to choke them when the candles are blown out.

I promise.

Love Fanny x

The shittiest birthday cake of them all. (Source: Google Images.)

Blue Lights and Red Lipstick.

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I don’t like to do things by halves. If you’re going to have cancer, you may as well do it properly, so I’ve been in hospital these last few days with neutropenic sepsis. Much to the disappointment of our children, who were out playing a football match, they missed a very dramatic ride in an ambulance as I was rushed off to A&E (but not before I’d left a present and card on the kitchen table for one of them to take to a birthday party that afternoon, because, you know, motherhood.) Like most women, I’ve always been fearful of having my jeans whipped off by a handsome paramedic on a hairy-leg day, but the chemo has sorted out that problem for me. My blood count had dropped so low that the common cold I caught last week could very well have killed me, but hey – at least my legs are smooth and shiny. As is my head.

Infection is a well-known complication of chemo, and easily fixed with antibiotics and blood-boosting injections, and because our children have already lost a parent, I didn’t mess about or wait a few hours when my temperature went up. By the time you read this, I’ll be home. They can save lives at our local hospital, but they can’t provide wifi. That’s a trade-off I’m happy to take, although our adolescent twins would probably think twice.
A few days before my admission, I’d been feeling really fed up. This latest recipe of chemo has floored me with flu-like symptoms, and a general feeling of exhaustion. I’d been fantasising of a nice lie down in a hotel room, with the boys and dog taken care of. Just me, on my own, relaxing with a book or two. I’ve decided not to make any more wishes as they obviously get lost in translation.

To keep life normal for the boys as I go through chemo, I’ve still been playing Mum’s Taxi, I’ve still worked full time from home, still attended school events, still watched them play football and cricket, still walked four miles a day with the dog, still played badminton with them in the garden, and I’ve even driven the three of us on a fourteen hour round trip, and spent two nights in a hotel, to attend a family gathering on the south coast – because if I carry on as normal, paint on some eyebrows, pop on a hat, and don’t behave like I’m ill, then I’m not ill. Right?

Wrong. The last few days have been an eye-opener, and a lesson in self-care, to say the least. Much as I remain impressed with our amazing NHS, I don’t want to come back into hospital again. I was placed in Protective Isolation in the world’s most uncomfortable hospital bed, and until the IV antibiotics started to work, and until my temperature came down after 36 hours or so, I didn’t even have the energy to read or write. Fortunately, Twin 1 very kindly loaded up his iPad with films for me to watch. His choice, not mine – a handpicked selection of movies about aeroplanes, terrorism, and a documentary on brothels.

I wasn’t allowed to drink tap water (and sterile water is, well, fucking disgusting) but they did let me wander up and down the corridors to keep myself moving during the long and miserable nights – partly to ease the lower back pain of lying down for too long, and partly so I could perfect my Lady with the Lamp impression, but with a drip, and a less attractive silhouette featuring one boob and a bald head. Oh, and there was always a people-watching opportunity outside Maternity, as the expectant mothers squeezed in one last cigarette just before the baby’s head started to crown.

Family and friends have been wonderful, as ever, and rallied around to help us, but my Mum and Dad live two and four hours’ drive away, respectively, and it can take some time to mobilise family troops. The reality of the situation here remains the same. No amount of eyebrow pencil, no supply of sparkly headgear, no carrying on regardless, can change things on a day-to-day basis. It’s getting tougher. When my husband was ill, he had me to keep everything going, and I remember so vividly that he said it was harder to be the carer. I think he’s right, but I’m now the patient as well. Having an ambulance sent for you because you’re alone; having to miss your kids’ football match (and then having to start making panicky calls from the back of said ambulance, under the blare of the sirens, to try to get them brought home and looked after,) and leaving some cash for them to go to the chippy for lunch because you’ve been too tired and weak to go to the supermarket (my Parent of the Year award is in the post) is properly, properly shit. The boys have eaten nothing but crap, and barely a vegetable or a vitamin has passed their lips, for weeks and weeks. I’m hoping that’s one of the fonder memories they’ll have of Mum’s Chemo Days.

On admission to hospital, I was asked about my marital status, and my next of kin. I should be used to the questions by now, but I still hesitated. I didn’t really want to say the answer out loud. All I know is that the tears came yet again as I let them tick the boxes about alcohol intake and stool consistency, and told them why I was there alone; that my real next of kin was dead. That the last time we raced to A&E, he was here, in the cubicle opposite the one I was now in. Just like him, I came in with a high temperature, collapsed veins, and a bald head, but this time, without a spouse to hold my hand, or to go in search of magazines and coffee machines. To carry the load of responsibilities still waiting at home.

I’m home now, where life is our own brand of normal. Where I can keep busy with work, and start every day in heels and war paint, once I’ve walked the dog. Where I pretend to the boys that I’m OK, because none of us can bear the alternative. Where I came out of hospital to a huge pile of work, but three hours after discharge returned to A&E with further complications. Everything was sorted without another admission, and I returned home in the early hours to find the boys sleeping side by side in mine and their Dad’s bed, for comfort. I slept in Twin 2’s bed instead – which definitely wouldn’t pass any Infection Control inspection.

My parents have done a brilliant job of keeping things going, even though the boys associate Grandparental Visits with Dying Parents, and respond accordingly, like proper little shitbags. Because they’re frightened. Because when their Daddy started to get taken away in ambulances, and grandparents arrived to help, he died soon after. They’re taking their anger out on everyone, especially me – as I did with my husband and children, when I thought life couldn’t get any worse. I was angry with the cancer, not with them; but I couldn’t always differentiate, and nor can they. How I wish we could go back to those days when being a family of four with terminal cancer was so much better than this.
When my husband and I could still be parents together.

Six weeks more of chemotherapy. Six weeks more of pretending I’m fine for the sake of the boys, but being a little more careful with myself to make sure I really am – because they will suffer the most in the long run if I’m not. I’m almost at the end of the road, and the end of this road will be the start of a new beginning, but perhaps I need to trade the heels for slippers, wear pyjamas more, bare the reality of my pasty and puffy chemo face, and admit that I’m not finding it all so easy.

My husband called me Wonder Woman. (He also called me TwatFace.) He knew I’d be OK, that it was safe to leave us, and that the boys would be alright in the end; that I would throw my heart and soul into the vacant position of Dad. He didn’t realise I’d go so far as to chop off my boob and shave my head to get into character, but – as I said – I don’t do things by halves. In a few weeks, Wonder Woman will be reborn – with a new razor for her legs, some hairspray, a sparkly scarf, and a brand new shade of lipstick.

Love Fanny x

Dedicated to Karen, who loved my husband, loved me, and encouraged us to love each other, despite the challenges which lay ahead. Who went to hospital last week, and wasn’t lucky enough to return home to her beloved family. A true Wonder Woman, and champion of the world. Rest in peace, my friend. X

New Seasons and Sick Bowls.

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I fucking hate spring. I used to love it. The joy of a new season. The green shoots. The blossom. Daffodils. New life. 

The last few springs have brought new life for our family, but not the one we wanted. In spring, they told my husband that he had a very difficult cancer to cure, but they were going to try. The following spring, they told us he was terminal. The spring after that, he died. Every spring, we’ve walked out of hospital grounds, as daffodils poked through the earth, feeling as though our own earth had been shattered. Spring hasn’t shown us its beauty for years.

This spring, the same pattern begins for me, but most probably with a more positive outcome. I’ll see next spring, and several after that. This spring marks almost a whole year without my husband, and I’m trying to make sense of this first, but surrounded by the same ingredients which took him away from us forever. Ingredients I never thought I’d associate with myself, or with any kind of future, come to that. But in an unusual twist of fate; without them, I may not have one at all.

Sickbowls. Hair clippers. Ondansetron. Epirubicin. Daffodils. Cyclophosphamide. Aprepitant. Palmar Plantar. Metoclopramide. Cannula. Mouth like the bottom of a bastard birdcage. Docetaxel. Constifuckingpation. Flowers. So many beautiful fucking flowers.

Side effects I’d forgotten my husband had had, are now mine. Side effects I’d wanted to forget – because, you know, it was too much to watch from the sidelines – are back in our home in full force. In fact, I think it’s easier for me now than it was then, because I understand it all so much better, and at least I don’t need anyone to hold my hair back when I’m throwing up in the night. I haven’t got any. (Although I still seem to need to shave my bloody legs. Where’s the actual justice?)

Yes, spring is a new beginning, alright. Every year, the start of a new life. A different life. I’ve always been one to embrace change with open arms, but – for fuck’s sake.

My husband and I had a fairly significant age gap, which was rarely a problem because we fell in love with each other’s minds, and the occasional discrepancy in physical stamina was our only real issue. But it did mean that, from an early stage in our relationship, we’d accepted the fact that – should life run its natural course for both of us – I would be left on my own for quite some time. There was never any question, at all, that my husband wanted me to move on, should he die first, and I felt the same about him, should I die early. You know, from cancer or something. We loved each other too much to wish lonely widowhood on the other, although we did often recognise the disappointment that neither of us had had the foresight to marry an octogenarian multimillionaire with a heart condition, instead of the skint and scruffy person we’d actually fallen in love with, 25 years out of sync. (But that was the point. We were in it for love. Nothing more.)

Telling the person you love that you want them to move on, should you die, is easy. It’s actually quite heartwarming, when you’re sitting in the garden, or on a hotel balcony, chatting over a glass of wine, and talking of an imaginary scenario years into the future. You know, when you’re not actually dying. When you’re completely full of life.

When that prospect becomes reality, it is heartbreaking. My husband held my hand, in his final days, in the makeshift hospice of our sitting room, and asked me to see his death as a new beginning. His beautiful blue eyes looked into mine, and he told me he loved me; that he always had, and that he’d be up there, sitting on his cloud, strumming his harp, watching us move forward, with love. He didn’t want to be missing from our future family portraits any more than we wanted him to be, but grudgingly accepted his time to go. All he asked was that, whoever it was, any future husband would be kind to his darling boys. That was a given, though I couldn’t picture a future husband at all.

I can’t imagine being with anyone else. Perhaps, under normal, non-cancerous circumstances, I might have been thinking about a different future by now, as the seeds of new life grow outside our window, because the lack of adult companionship, day in, day out, can be lonely and isolating. Especially now. But in my heart, I’m still married to my husband, and still faithful. Our bedroom hasn’t changed at all – except for the thermometer which has moved from his side of the bed to mine, with the Chemotherapy Hotline number still inscribed upon it in my husband’s hand. He and I are inextricably bound to each other by our children, who fear for a future without their last surviving parent. We’re still bound by those memories of a cycle of treatment which goes on and on. And on. And on. In some ways, these memories help my husband to hold my hand through it all, in the only way he can; from his celestial cloud (with the other hand strumming his harp.) Nobody else could take his place, because this is his place. He holds me through the treatment in my veins. The pills I take every day. The hair falling onto the sheets. The blossom falling from the tree.

He is still with us. Our hopes and our new beginnings are not what we ever imagined them to be, but he is still a part of them. Every spring, and always.

Love Fanny x

With every new spring, new sickbowls appear…

Brian May’s Merkin

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This has just happened. 

After only a few days on chemo, I’m taking control of the hair loss situation with a pre-emptive strike, and I’m jumping before I’ve been pushed. Now I’ve done it, I’m not sure which would have been worse – waking up among ever thicker clumps of curls on my pillow, day after day, or the resultant ‘do which has seen me go from Tim to Edwina Currie in half an hour flat. I’m not quite rocking the Matt Lucas just yet, but give it a week or so.

We’ve been here before, with my husband, and we could always tell when the hair loss was a few days away when the pubes started to appear around the loo seat with alarming regularity. They were always the first to go. My somewhat unruly Widows’ Bush still passes the tug test for now, so I reckon it’ll be a few more days before anything happens on my head. Not that I’ve really spent an awful lot of time tugging.

I honestly thought that losing my hair would be the easy part. The mastectomy had been the frightening bit, because – before it happened – I thought it meant losing everything that made me a woman. The hair wasn’t a problem. I was up for it. In fact, I’d go so far as to say that I was almost looking forward to choosing a cute little Audrey Hepburn pixie crop ahead of The Big Shave, and not having to dry the ridiculously thick, unruly mane I’ve learned to cope with over the years. After spending a large fraction of my waking life with my head upside down over a diffuser, a quick polish and go was beginning to sound appealing.

But that isn’t how it is. On a daily basis, since my op, I look in the mirror at the scar where my left breast used to be, and I feel OK. Early on, I realised that the boob had never, actually, made me who I am. And anyway, it’ll be back, nipple and all. In the meantime, I pop in a Knitted Knocker and off I go. I’m more bothered by the half a fucking stone that I’ve put on in the last few weeks. Seriously – losing the weight of my (admittedly fairly small) left boob seems to have made absolutely no difference at all, which is one of the greatest disappointments of my treatment so far, but that can be dealt with later.

Our boys have seen what’s left of me. I was determined, from the start of all this, to carry on as normal. We’ve always been an open family, and as they were growing up (OK, partly because my husband and I were far too tight to pay for interconnecting hotel rooms on holiday,) they’ve seen us in all naked shapes and sizes. They’ve seen us both at our chunkiest, at our fittest, and even felt the severe muscle wastage towards the end of my husband’s life, as we all smothered sun block onto ourselves in Lanzarote three weeks before he died. Fucking Lanzarote. It wasn’t just the sun we were blocking out. When we got home, they knew deep down, because they had seen it for themselves, that their Daddy had to die. I think we probably all did. They had to learn, at too young an age, that a fabulous body was nowhere near as important as a phenomenal mind, heart and soul, and their Daddy had those three things in abundance. To be fair, a great bod had never been quite his forte.

Over the last few weeks, I’ve made sure that the boys have seen my mastectomy scar as part of me. I feel fortunate that they’re still pre-pubescent, because I don’t suppose that their seeing me in various degrees of undress is something any of us would want in a few months’ time. At first, I suppose I eased them in gently, and it was just something they might have spotted if they were hanging around upstairs as I got dressed. No big deal. But yes – there were comments, as only 11 year old boys can provide. Now, they see it all the time, and nobody notices it any more, as I casually hop into the shower, or as I run down the landing half naked to bellow at them to get their fucking shoes on. I didn’t want one missing tit to be a big deal for them. I wanted them to see me, to know me, and to love me, just as I am now. I wanted them to realise that – heaven forbid – if one day they were to support their wife or girlfriend (or boyfriend – I’m very modern) through something similar, that loving their partner anyway, no matter how many missing body parts they had, would be the most natural thing on earth.

Still, when I returned from my oncology appointment the other week, and told the boys that yes, chemo would be of “indisputable benefit,” one vomited and went to bed for 24 hours. The other got into a fight with a friend. They were angry, worried, and upset – not about the pending sickness and tiredness, but about the fact that I was going to let the doctors do something to me which would make my hair fall out. I promised them that it would grow back, that I’d wear a hat in the meantime, and that they could even see the wig I’d chosen. They didn’t want to know, and I didn’t understand why the hair loss – of all things – bothered them so much, when the thought of it hadn’t been bothering me much at all. But, for the boys, cancer means chemo. Chemo means bald. Bald means dying.

Now, as the remains of Brian May’s merkin lie on the floor, and I look in the mirror, I can see it. I understand. I know what panics my children, and the fact is that no wig, no hat, and no prosthetic boob will hide it. Their mum has cancer. Their dad died, a few months ago, looking much like I will in the next few days. They’re not old enough, or strong enough, or confident enough, yet, to allow themselves to believe there will be a different outcome for me. They don’t care if I have a left breast or not, but until my hair grows back, they will know I have cancer. It’ll be written all over my face. They will remember, and that will hurt us all for far longer than it will take for my body to be slowly pieced back together.

Love Fanny x

The Only One-Titted Widow in the Village.

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Today is World Cancer Day, apparently. A day to raise awareness, though some of us are painfully aware already, thank you very much. I agree with it, in principle. Read their literature and educate yourself. Know the signs. Early detection is key, so don’t be afraid to visit the doctor. As a friend or relative, understand how you can help people who are going through treatment, or are recently bereaved. Avoiding the issue won’t make it go away, and not every cancer is treated with chemotherapy – many cancers are easy to get rid of, and the earlier they’re found, the better. 

My recently bereaved eleven-year-old son has been using cancer to his advantage (and not just by wandering over to the pastoral centre at school every time he wants to get out of a lesson he’s not particularly keen on.) Having realised that my NHS-issue prosthetic boob, even with the stuffing removed, was too big for my bra, he’s been profiting from this problem, and was spotted wielding it at school and charging 5p for a feel. His daddy would be proud of his entrepreneurial spirit in the face of adversity, but would undoubtedly have charged a hell of a lot more. It used to take at least two bottles of wine and a night out to get me to whip my tits out, when they both existed, so 5p seems like a bargain. At the blood donation centre, my husband and I used to snigger every time they asked if either of us had ever paid for sex. We wondered if the Audi or the new coat from Karen Millen counted.

I doubt that anyone will be paying anything to see what’s left of mine now, which is fortunate, because the man who loved them the most is dead, and today – as every day – I fall between two very shitty stools, as a widow with cancer.

On the internet forums, the cancer widows seem pretty quiet about World Cancer Day, and I can’t blame them. They probably feel like I did, when my husband died. Why raise awareness about it now? Why fundraise for research or support? It’s a bit fucking late for us. Cancer Research funded the unit where my husband and I went, week after week, dangled on a string of hope, when there wasn’t any hope at all, and they knew it. I know this now too, because he’s dead. So, instead, we fundraised in his memory for people who would have given anything to trade places with us – to die in a warm bed, safe and surrounded by loved ones, rather than spend their lives shivering in the cold on the streets of Manchester, or fleeing bombs and persecution in war-torn Syria. My husband knew which side his bread was buttered on. He had been lucky. Having said that, I don’t want to die of cancer, any more than he did. Cancer is a horrid and lingering way to go. It’s why, every day, I tell my kids how much I love them; it’s why I’ve written a will, and why I’ve given my important passwords to someone I trust. I’m hoping that an aneurysm will get me instead, many years from now, quite suddenly, but not so suddenly that I haven’t yet got around to throwing away the sex toys that are gathering dust in the back of the wardrobe before the children come across them when they’re sorting out our stuff.

Yet now, as a cancer patient myself, things have changed. Suddenly, I’m grateful for the research into cancer treatment because I know that it will give my children the best hope of keeping one parent alive, even if it didn’t work for the other. I’m not suffering in the way I saw my husband suffer. The pain of the bereavement is worse than the pain in the wound where my left boob and lymph nodes used to be (which is still fucking painful, by the way,) but it isn’t so all-consuming that death would come as a relief. Of course, there are no guarantees that I’ll survive, but there are no guarantees that I’ll make it alive to Sainsbury’s tomorrow either, given the way that some people drive. My surgery results are in, though, my margins are clear, and the chemo I’m about to have is – like most post-op chemos – precautionary. My husband’s wasn’t. His margins weren’t clear, and he endured several rounds of palliative chemo. I probably won’t die, as long as we mop up all those stray cells before they’ve the chance to settle anywhere and grow again, and having hope (I mean, real hope) is something I’m incredibly grateful for. Those impending few months of baldness and nausea are a means to an end, and I’m damn well taking them if that’s all I need to do. I can do six months on chemo. My husband did four times that, on and off, and still worked full time until two weeks before he died.

I don’t feel much of an affinity with the internet widows any more, because I can’t remember how it felt when bereavement was the only worry I had. But, the breast cancer forums are far worse. Oh, fuck me. The Breastapo. They’re all warriors, that lot. By definition, these groups are mainly populated by “survivors” and don’t we know it. The Goddamn memes they post about how they’ve managed to get through something they thought would kill them, and how fucking clever they are. Well done. They – like me – turned up to some appointments and let highly qualified people do what they needed to do to cure their (in many cases eminently curable) cancer. It doesn’t make them brave. It makes them normal. Don’t get me wrong, they did the right thing to go to the doctor, and having cancer is as scary as shit, and I am thrilled that they’re OK – not only for them and their families, but because it gives hope to me and my children that I will be, too. But just as much respect for the people of all shapes and sizes who’ve dressed in pink and limped, waddled or run like gazelles around their local park to raise millions to make sure the research has been done to find a cure. So many of the posts I read are Titty Top Trumps. So how big was your tumour? Just four centimetres? Only three lymph nodes? Amateur. The pats on the back for their survival and bravery are, to a cancer widow with stage three breast cancer, pretty hard to read. And today I realised why. For many of these women, breast cancer is the very worst thing that’s ever happened to them. But it’s not the worst thing that’s ever happened to me. One thing I will say for the widows, nobody tries to make out that their husband or wife is deader than anyone else’s.

It is great that so many people survive. It really is. But less than a year ago, I watched my husband die, and he didn’t bloody well want to. The research isn’t as far on for oesophageal and gastric cancers just yet, and he missed the boat. Yes, it’s reassuring to feel solidarity from people who’ve trodden the path before you. But, going through treatment isn’t actually brave, so for fuck’s sake quit with the high fives and the smug memes. Going through treatment is necessary. Accepting that you need to give up treatment when there’s no more hope at all is what’s actually brave. Choosing a suitable spot to place the bed you’re going to die in is brave. Writing letters to your beloved children, when you’ve only got a few days left, and you’re going to miss most of their entire fucking childhood, is brave. Collecting your husband’s end-of life drugs from the chemist is brave. Agreeing to a DNR is brave. Letting the nurses insert a syringe driver is brave because you know it’ll only be taken out once the vein it’s pumping into has stopped working. Kissing your daddy’s dead bald head is brave, and watching his body being carried out of his beloved home under a fucking blanket when you’re only ten years old is really damn brave. Having to choose what coffin and flowers and funeral songs your husband should have is brave. Signing the form to say they could shove a pipe up his arse and embalm him is brave, as is providing the photograph and the clothes which will help the undertakers to rebuild him into some semblance of normality before they take his body to be burned and ground to ash.

Do you know what’s not brave? Turning up at a hospital as a grown adult with responsibilities, and accepting the drugs which will almost certainly make you better, because – you know – responsibilities.

A friend, and my husband, died from cancer in the last few months. My friend was dismissed over and over when she turned up at her GP with symptoms, and she died. My husband’s GP was his best friend, and gave him the best attention and care that he could, but he still died. Neither could be saved. Those two wonderful people, who were physically strong; who adored and protected their kids, and who were fiercely loving of life and their families, both died – with levels of medical care at both ends of the spectrum. Did they not fight hard enough? Yes, they absolutely did, but sadly their cancers weren’t as treatable as mine.

If you’re lucky enough to be able to post one of these stupid memes on the internet about how strong you are, well done, but don’t forget the ones who can’t post anything, on account of their being too dead. I hope, one day, I’ll be lucky enough to be able to post one, too. But I won’t be posting anything, except gratitude for those who did whatever they could to fund or do the research which made my survival possible, whether they’re strangers running across parks in pink tutus, or friends turning up with sets of hair clippers and comedy wigs to keep the tumour humour alive. But I also hope I’ll never let this year of treatment define me as some sort of warrior. Once the hair grows back and the left tit is stuck back on, I want to move on, buy a new bikini, and barely mention it again. I’ll always advocate early detection, and support friends going through cancer in the future, but I’m so over it.

Some battles can be fought, but this one is indiscriminate. Without any weapons in our arsenal, we’re never going to win, no matter how “bravely” we face the oncoming hordes of bad cells. For now, I remain out of place as the only one-titted young widow in the village, with my husband’s ashes in one hand, and my kids holding tightly to the other. Thanks to all who’ve done their bit to make breast cancer a more survivable illness, I don’t have to free my hands to grab onto a white flag instead. I hope I’ll never have to.

Happy World Cancer Day, to those who are no longer here. We miss you like hell.

Love Fanny x

Just a little amendment to a smug fucking meme. You’re welcome.

Three Chicken Fillets and a Pencil Test.

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It’s almost a week since my mastectomy. And do you know what? I’m actually OK. The worst thing that was going to happen to my body, ever, has happened. My left breast has gone.

It was bad enough, almost twelve years ago, when – having sat through NCT meetings, smugly proclaiming that I wouldn’t be having any pain relief and heaven forbid a Caesarean section – I had to be knocked out cold to have two babies ripped from my womb in a dire state of emergency following a placental abruption. As parents of IVF babies, we were the only couple we knew who could honestly say that we hadn’t been either present or awake for the conception or the birth of our own biological children. Although I was traumatised by the boys’ birth for weeks, and cried buckets over the loss of the one experience I’d so desperately craved, I soon learned to love our babies so much that it didn’t matter how they’d arrived in the world, because they’d arrived alive. And my husband couldn’t help but admit that he was rather pleased I’d managed to deliver twins, yet still avoid ending up with a fanny like a clown’s pocket. 

I feel the same about my breast. I didn’t think I would, but I do. It’s OK. I’m OK. Sore and tired, but OK. The greatest pain comes from where they took my lymph nodes, not from the breast area itself. For the first couple of days, I couldn’t bear to look at what was left. I cried when they woke me up from my operation, and when my friends came to the hospital to collect what was left of me. The wound was covered with dressings, and it still will be until they remove them at my results clinic on Friday, but the flatness is something that can’t be hidden. I’d been showering as normal, but making sure I avoided going anywhere near the mirror.  

About three days in, I decided to look. And the good news is that I definitely still pass the pencil test.  

It’s a little like when you meet someone who has an unusual face. At first, you think, oh fuck. And then, after a while, you stop noticing. They just become who they are, and you love them anyway – because of their faults, not in spite of them. We all know enough supposedly pretty people who are ugly inside, and vice versa, that the soul is always what shines through the most strongly, and I refuse to have mine tainted with bitterness and anger. This new land of uniboobity hasn’t changed who I am in the slightest, and nobody’s more surprised about that than I am. I’m determined to keep my soul intact; to learn and grow, to find some positivity in all of this (fuck knows what,) and to choose how I deal with my life experiences. I am not a victim. I’m not a warrior. I’m still just me. Unevenly-cleavaged me. My husband’s soul is holding mine tightly, and through asking myself what he might say, I’m finding the strength to love the imperfect me as I loved – and always will love – the imperfect him. He really was imperfect (I mean, for fuck’s sake, aren’t they all?) but I’d give away my other boob if it meant I could have him back again. I can’t. So what now? I can’t change my past, but I can take control of my own happiness. Within all this pain, something good must come. Otherwise, what’s the point in going through it at all?  

Maybe if I thought they weren’t going to reconstruct my breast after my treatment, I’d be mourning it more. But, the worst thing that could possibly have happened to our family, already has. My husband has died. What’s worse than dying? Not a lot. There’s absolutely nothing left of him, yet we still love and want him more than ever. At the moment, I’m trying to be the best mum I can be with temporarily limited mobility, and I’m even up and about, doing a bit of work, and cooking meals for the three of us. Chicken fillets, obviously. 

What I’ve got – well, it’s only cancer. Not terminal cancer. So, I remain grateful. I’m going to put my best boob forward and carry the fuck on. 

Love Fanny x 

The One Tit Wonder.

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I’m having a mastectomy in the morning. My left breast is going to be removed – completely. In a few hours from now, you may legitimately refer to me as The One Tit Wonder. Although I wish my husband was alive to love me through it, I also know that my ability to perform a soapy tit wank will be temporarily suspended, so he definitely had the best of me, and I should probably welcome the timing. Since I’m going to spend the rest of the year with one boob, a dry vagina (apparently one of the main side effects of my forthcoming hormone treatment) and bald from chemo, I doubt that I am the North of England’s Most Eligible Widow at this point, anyway. I’ll be holding him in my heart through all of this, if not in my cleavage.

I’m finding all this pretty hard to take, but I know it has to be done. I also know that, had I just gone ahead and booked myself in for a mastectomy with immediate reconstruction back in August when I was diagnosed, I might have already woken up a few months ago, cancer-free and with a new breast. But, I panicked. I couldn’t come to terms with having cancer less than four months after losing my husband to the same vile disease, and delayed, and tried to do anything I could to save my boob. But it didn’t work, and the three little Stage One tumours they thought I had are actually one large, late Stage Three tumour – in my skin, my chest wall, and my lymph nodes. What couldn’t really kill me before, now absolutely could.

The day before I went for nipple and breast-saving surgery, a friend of mine died from metastatic breast cancer. And I know that, with or without her boob, her family would give anything to have her right back here. That’s exactly how I feel about my husband, and I’ve written about it many times before. In his case, he lost his oesophagus and part of his stomach, but he was here, and I loved him. And now he’s not there (but I still love him, and miss him desperately – as do our young sons.) He could have had a leg or an arm or even his willy removed, and I really wouldn’t have cared. Well, I might have cared if he hadn’t had a willy, but we’d have coped. He was so much more than one single part of him could ever have been.

I didn’t think it could happen to me. It doesn’t happen that way, does it? Kids sometimes lose one parent to cancer, but not two within months of each other. Well, it bloody well does happen. I’m lucky – I’ll survive this, with a fair wind and a decent cocktail of drugs, and provided they take off the right tit. (By which I mean the left tit. Please, God, make sure they take the left one.) Later, I’ll have a new one, but I’ll have to live with a bra full of sponge for the time being, because they tell me there’s no point in rebuilding something that’s going to be damaged by radiotherapy, and I must wait until everything settles down. I even have my little pink bag of shame packed inside my hospital case, with a regulation-issue mastectomy bra and a wad of sponge for me to add to or take away from as I see fit, when it’s all done. I fucking hate it already. My tits are brilliant. Were brilliant. I don’t want to swap one of them for a fucking sponge.

So, what I want to say to you is this. Feel yourself. Go on. You’ll feel a bit of a twat, especially if you end up at the doctor’s, but don’t worry. If you think you’re lumpy, or spot any changes, just go and get yourself checked. Doctors aren’t magicians; they’re only human, and it took me three visits to be finally diagnosed. Medicine can be quite hit and miss, but you’ll definitely miss if you don’t go in the first place. Don’t be embarrassed. Doctors have their fingers up people’s arses on a daily basis, so what makes you think yours is so special they’ll remember it? Ask Dr Google and make your web search history even more interesting. Know the signs. Whether it’s your boobs, your bowels, the top of your leg, or the end of your penis, it really doesn’t matter. It shouldn’t have happened to me, but it did, and my dithering and flapping and grief could have cost me my life. My husband and I both told the doctor as soon as we’d noticed symptoms, and in my husband’s case it was still curable, but only just. Oesophageal cancer is impossible to spot until it becomes hard to swallow, by which time it’s often too late, but we still had an extra precious year thanks to him acting when he did. Hopefully, we’ve got mine in time. So, seriously – what’s the worst thing that could happen? You’ll die. That’s what.

I live every day with two little boys who cry and scream and fight their way through the heartbreaking consequences of terminal cancer, and I owe it to them not to let them see me through it as well. It might be slightly embarrassing to go to the doctor, but believe me – the process of death is far worse. No matter what happens – whether you have life-saving surgery, or you end up in a hospice – you’re going to have strangers faffing about with catheters, so make sure they’re doing it to keep you alive, and not just to make you comfortable. And if you’re fine, you’ll be relieved, and there won’t be any catheters at all. If I’d been in an accident and the only way to save me was to saw off my leg, they’d have done it there and then and asked questions later. I have to remember that this is the only way. I wish my husband had only lost an extraneous body part, and not his whole life, because by losing him we lost everything that made us a family.

It was never the right time to let go of my husband, and it’s not the right time to say goodbye to my left boob. But, I have to remember that it’s only a tit. My husband thought it was fucking ace, and we did have some fun with it and its counterpart over the years. Most importantly, though, it fed and nurtured our children, and if I let it go now, I can continue to do that for many years to come.

Love Fanny x

 

2017-01-08

A useful infographic from http://www.breastcancercare.org.uk. Go on, have a feel. You know you want to. And when you’ve done that, check everywhere else. Visit http://www.cancerresearchuk.org/about-cancer/cancer-symptoms for more information.