Fanny for Grabs.

A few weeks ago, I did a deal with my son. My angry, grieving, difficult son. It wasn’t a deal I wanted to do, and – in many ways – it felt like a pact with the devil. I told him that if he would engage with a course of counselling, then I’d do what he’d been asking for, and start to look for a new partner. 

I knew that it would take several weeks to sort out my son’s head, and, through counselling, he’d probably realise that his problems were not going to be easily solved by my acquiring a substitute for his dad. I wasn’t ready for a relationship, and was otherwise muddling along as a double – not single – parent, but at my wits’ end.

Both boys have been desperate to see me happy again – and that, they believe, means for me to be married off as quickly as possible. Even when my husband was still alive – on the day we sat the boys down at nine years old, and told them their Daddy was dying – one of them disappeared with the laptop to look for a dating website so they could find me a new husband as a matter of some urgency. It took a little while to explain the concept of marriage vows, sickness, health, and death us doing part etc., but we got there in the end.

Since my husband died, though, the boys have made several less-than-subtle suggestions. On holiday last year, barely four months after I’d been widowed, they danced around me singing Love Is In the Air while I was having a perfectly genial conversation about table tennis with a 19-year-old member of the Croatian animation team. They’ve come home from school full of optimism every time one of their friends happens to have a set of parents in the throes of divorce. On the holiday we’ve just returned from, I sat in the bar most nights being elbowed in the ribs by an enthusiastic twelve-year-old who had spotted the multi-millionaire Saudi Arabian fortysomething with a penchant for $160 shots of cognac. Although he seemed like a nice guy, and we found commonality in being widowed parents of teenage boys, I couldn’t quite shake off the thought that anyone who could spend $160 on a single shot of cognac was probably more than a bit of a twat. All I wanted was a cuddle and a conversation with my ageing scruffy intellectual, who was usually floored by half a lager – the cheapest one available.

I’ve apparently had sniffs of interest via friends – which has been flattering, but unreciprocated. I’ve just not been ready to even contemplate a relationship with someone other than my husband. Since we interred his ashes in the churchyard a week after my treatment ended, though, I’ve felt an element of closure and optimism that I haven’t felt for a long time. I miss him, terribly. I always will. But he is dead – and burying a box in the ground with his name on it hasn’t brought him back to life, much as we all wish it could have done. Now, with every new hair that appears on my head, I feel a strand of hope; of a future which is new, exciting, and seems to be within my grasp. It’s been such a long time.

A few weeks ago, having returned from another very lonely holiday in which the children mainly made friends and buggered off, just as I’d expected and wanted them to do, I asked my husband’s dearest friends for advice and reassurance about the next tentative step I thought I might want to take. Without exception, they gave me a monumental thumbs up, and later that night, I got myself royally pissed and set up an internet dating profile.

I met my husband at work over 16 years ago, at a time when entire families were sharing a single dial-up internet connection, so online dating is completely new territory for me. As a widowed parent working from home, though, it seemed like the best place to start.

I knew that my husband had wanted me to move on after – and I quote – a “suitable period of mourning,” but my mourning period has been long and difficult, and isn’t over yet. It never will be, completely. Nonetheless, I was nervous as I filled in all the criteria (including an upper age limit of 48 – the age my husband was when I met him,) and selected that any potential suitor must be educated, and that he must have a proper job. There was no option to request that he have no pre-existing medical conditions, or a family history of cancer.

Out of about 25 possibilities, only one face leapt out at me, but I duly went through each profile one by one. As more and more so-called “compatible” matches appeared, and as I read through each one (deleting them with gay abandon) it became clear to me that I had a few more criteria of my own, which couldn’t have been picked up by the website’s algorithms.

– He must have a nice traditional name, but not the one belonging to our dog.

– He must be able to spell and punctuate.  

– He must not be a Tory.

– He must not be topless on his profile picture, although bonus points for removing his anorak.

– He must not be wearing a football shirt.

– He must not still be proud to display one of those Celtic arm tattoos.

– He must use a picture of his face, not his car.

– He must not use “LOL” at any point, especially not as an appendage to an otherwise rather dull statement.

– He must write something to make me smile.

– He must be someone that my husband would have liked. A lot.

Likewise, I tried to answer all the questions as honestly as I could.

– I explained that I liked all types of music, but that I wasn’t allowed to like anything too modern on account of it being embarrassing for the children. I also warned that I’m rather keen on musicals – particularly reenacting certain death scenes at full volume during long car journeys – and that I tend to forget that I am not in fact a member of Little Mix.

– I listed my hobbies, which include refereeing arguments between twin boys, swearing, and being the world’s most unremarkable cook.

– I said I was widowed with pre-teen twins, and looking for someone who, like me, was not in a rush, but who would enjoy intelligent debate, wine, sarcasm, and companionship. I also asked that he should be a dab hand at DIY, an enthusiastic grammar pedant, and enjoy getting up early to let the dog out.

I decided not to mention the missing boob and ghastly post-chemo crop at this point. I expected the search to take several months. I also knew that anyone who could jump unscathed through all the hoops would be a chap worth getting to know better, and if he still managed not to care about how many mammaries I currently possess, then that would say everything I needed to know about him.

I whittled my own shortlist to a grand total of one. A tall, handsome, marathon-running scientist, with an attractive smile and a self-effacing biography, who also happened to live the closest to me – just up the road in the next valley. The one whose picture had stood out in the first place. He was probably way out of my league in intellect and looks, but I’ve learned that life’s too short to not even try. We exchanged messages, and I was relieved to find that he used the correct version of “you’re” in a sentence. He had found my profile to be quirky and interesting, although I’d made the first move – it turns out, if left to his own devices, he wouldn’t have given me a second look as he normally goes for leggy blondes. As did my husband. My husband had not been a health freak – in fact, he got out of breath running a bath – and that was often a stumbling block in our relationship. A whole new outlook on health from a partner would not be unwelcome, but in the long term, I want a man who can stimulate my mind as much as he can stimulate my somewhat imperfect body. A man as imperfect as me. A man as imperfect as – though different from – my husband.

I will report back. Even if nothing long-term comes of this, I’ve had the joy of communicating with another adult, on the same wavelength, whose epic banter (in exquisitely-punctuated messages) has made my heart leap and a smile reach across the full width of my face. Who knows what will happen? We’ve been on a few dates already, and the connection is strong. We miss each other when we’re not together. He knows the score. All of it. He’s had his nose in my Fanny for the last few days (which is absolutely not a euphemism) and still hasn’t been put off by the grief, the booblessness, or the frequently awful children. If all else fails, he knows he could end up as material for the next blog post, so he’s trying his best to not be too much of a twat. And so am I.

I wasn’t expecting to click with anyone so soon. In fact, I realise now that I wasn’t really expecting any kind of life at all. I’ve simply been existing, day to day, for three and a half years. Three months ago, I was quietly planning my own funeral (I was going to have Brimful of Asha as my coffin came in, by the way. I thought it would be funny,) but now I’m planning a future, and it feels wonderful. The boys haven’t met him yet (nor has he endured Trial by Friends,) but they’re delighted that we’re going out on dates and keep asking me why I’m smiling for no reason. And, they’re both still receiving and engaging with counselling. These are still very early days, but they’re good days, and – far from feeling like cheating – being with this man already feels like the most natural thing on earth.

In actual fact, it feels as if somebody, somewhere, has played a very special part in this. He knows that the time is right for the boys and me to smile again after so many years of pain. Maybe, a loving hand from heaven has given things a nudge in the right direction. Time will tell, and I have plenty of that.

Love Fanny x

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A Future for Fanny.

Following a few nail-biting weeks, I’ve just heard the two wonderful words which my husband never got to hear.

All clear.

Thank you to everyone who helped to drag me along the darkest path I’ve ever had to walk alone – in particular to The Fanny Pack, and to so many others, whose kindnesses will never be forgotten.

Thank you to friends, and strangers, who have joined me here on the blog, and supported the boys and me practically, at home or in hospital.

There is a new life at the end of the tunnel, and my wonderful, brave, much-missed husband is holding the light which guides us there. He always will.

Life, Part Three, starts here. (Well, when I’ve handed back my radiotherapy gown and finished setting fire to my wig.)

Love Fanny x

Chemo accoutrements, no longer required.

Blue Peter Boobies.

Almost as distressing as losing a left boob, my hair, and quite a lot of my dignity over the last few months, is the cost of mastectomy bikinis. Now, I’ve always objected quite heavily to paying handsomely for anything which is basically a couple of pieces of string and two cloth triangles to keep your tits held up on the beach, but holidays are the only time I ever seem to think about having my photo taken (weirdly, I tend not to capture the memories of everyday family life, such as shoving fish fingers in the oven, screaming at the kids, or filing away the gas bill.) So, it’s nice to go on holiday with a few decent clothes, and wear something that makes me feel good on photos and in the sun.

We’re now on our much-anticipated family holiday, which marks a new start for us all – and while I would probably have been happy enough to sit in a tshirt, just for the joy of feeling some warmth on my skin, I didn’t want to miss out on being able to splash around in the pool with my boys. They’ve had little enough of me lately as it is.

Marks and Sparks, and George at Asda, do a couple of good and inexpensive mastectomy swimsuits… but I don’t want a swimsuit. I’m not even 40. Even though I’m still in the process of shedding the Chemo Stone (not easy when there’s always free booze and a buffet) I want to wear a bikini. This summer, I’ve discovered that mastectomy bikinis are generally available on specialist cancer websites at around £120.

Having lost my husband to cancer and gone through a year of treatment on my own, I want our children and I to live our lives to the full – and spending ridiculous sums on a piece of cloth with a pocket in which to stuff my falsie is not part of the deal. £120 could buy us more days out and holiday memories, and making memories is something our family will never regret.

So, here’s what I made earlier. In light of the missing cleavage situation, I’ve bought some ordinary bandeau bikinis from a high street shop for about a tenner each. They have little pockets in the side with a boob-shaped insert, presumably to keep everything looking even, and to minimise the chilly post-swim “light switch nipple” situation.

I’ve stuffed some quick-dry material in the pockets (the same stuff as those exfoliator puff things you use in the shower;) enough to match the other side. It sits quite happily behind the insert, safely and comfortably, doesn’t lose its shape, and dries out quickly after a swim. You would simply never know. (And as a bonus, I don’t need to worry about my false boob falling out and bobbing around in the pool.)

It’s hard enough having to lose such an important part of my body, but it’s even harder when doing normal things like swimming become seemingly unaffordable. Although I won’t be able to wear anything with a cleavage until after my reconstruction next year, there’s no reason why I – and so many other women – shouldn’t be able to join in with the simple pleasures in life. I know I’m not a big lady, but given the way bandeau bikini tops squish everything a little flatter, I don’t see why it couldn’t work for everyone. I’ve also decided to keep the straps on, so it’s less likely to end up around my neck, half way down a water slide.

Nobody here has noticed that I’m any differently endowed than anyone else. I guess they will if I decide to pop up (or out) over here…

Love Fanny x


End of Part Two.

Today marks 1172 days since cancer came into our family. 1168 days since my husband and I walked through the doors of this hospital, hand in hand, for the very first time.

Those doors were the last thing my husband saw of the outside world, before being wheeled into an ambulance and brought home to die. He said, at that point, that a bag for life would probably be an unwise investment.

Today, 463 days since my husband died, and 343 days since my own diagnosis, I walk out of the same doors once again, on my own, to the outside world, for what we all hope will be the very last time. To freedom. To our children. To countless more days.

Here, they’ve given me the most precious gift – my life, wrapped up in a metaphorical box with a bow, when my husband couldn’t even begin to pick off the sellotape. Here, my treatment has finished, and I am cancer free. The words don’t even seem real, after so many days of nothing but cancer. It’s going to take a while to adjust.

To say thank you, I brought a big box of chocolates for my radiographers, and asked them to share it around my husband’s oncology team as well, in the room next door.

Next week, it’s our fifteenth wedding anniversary. My husband’s life in a box – the ashes which are all that remain of his hands, his smile, and his wonderful mind – will be interred in the church yard where we stood and kissed for our wedding photographs, and where his dearest friends carried his coffin as we said our goodbyes. In sickness and in health, I was with him, and he with me. Maybe it’s time now to let him rest.

Until my husband and I meet again, I’m going to do one thing – for him, for our children, and for me.

I’m going to invest in a bag for life.

Love Fanny x

One Fried Tit and a Healing Scab.

For two years, my husband and I went back and forth to the cancer hospital, through roadworks, down motorways, along side roads, and always into the same bloody car park. Back and forth. Back and forth. And then we waited. And waited. Their admin was dire. Their queuing system was dire. Their coffee was dire. But, the staff were lovely, and the relationship we had with my husband’s oncologist was great. Well, we knew each other very well in the end.

When we reached the end of the line – when it became clear that no more treatment could be found to save my husband – his oncologist told him that he needed to be admitted for a day or two; have a scan, and maybe a lung drain, and that we’d reconvene in a couple of days. Although the doctor’s message was clear to me, my abiding memory is of my husband being wheeled down the corridor to the ward, after the seventh failed attempt at cannulation. He turned around to grab my hand and said, “let’s not give up hope yet.” He couldn’t be dying. We’d just come home from holiday. A week before that we’d been riding rollercoasters in Blackpool. He wasn’t ready to die, and I wasn’t ready to let him.

But, there was no hope. I knew it. The oncologist knew it. All the nurses knew it. Over the course of the preceding weeks – when my husband was on a clinical trial which we thought might be the answer to our prayers – the oncologist hadn’t always been very direct, and we still clung on to the hope that a miracle was around the corner. 
A couple of days later, when we left the building for the very last time, we’d both commented that, at the very least, it was a relief that we’d never have to go back to that fucking place ever again.

How wrong we were. I now have daily visits to that same hospital, but without my husband to hold my hand. Parking in the same car park. Passing the café where we used to sit and drink awful coffee and wait for blood results. Walking past the same ward where I took one of the last photos of my husband, working on his laptop, tying up some loose ends. (We pissed ourselves at that, and he posed for the photo gladly. “I’ll rest when I’m dead,” he said.) I pass the BEREAVEMENT SUITE. It’s a hospital – of course there’s a bereavement suite – but just in case you’ve forgotten that this is a cancer hospital, it’s written there, just by the entrance, in massive jolly writing, so you never quite forget that there’s a chance of BEREAVEMENT the moment you step through the fucking door. (We never actually went into the BEREAVEMENT SUITE because my husband died at home. Our sitting room is our BEREAVEMENT SUITE instead. I never go in there now, either.)

I’d managed to avoid the cancer hospital up until now, apart from a brief visit to check that my heart was in good enough shape to start chemotherapy. How ironic, I thought, that they needed to check the condition of my heart in the very place where they broke it. I’d been fortunate, in a way, that my surgery was done in our local hospital where they also have an excellent chemo unit, and they moved heaven and earth to make sure I didn’t have to go back to the place so full of difficult memories. Until radiotherapy.

I was expecting to be able to have that treatment at one of the local satellite centres too, but my oncologist wasn’t happy. She said my tumour had been too large, in too awkward a place, and she wanted to fry not only my left tit, but also my neck and my chest wall, to give me the greatest chance of survival. She wanted me to be in the best place for the treatment I needed. The best place? That best place also happened to be the place where they couldn’t cure my husband.

So, there I go. Every day for three weeks. I walk down the corridors, in a building which was so very much ours. It’s not somewhere I ever wanted to be ours, but bringing a friend with me now would make me miss my husband even more, so I go alone.

On the first day, I walked through the same door, into the same waiting room, with the same writing on the board, stating that my husband’s oncologist’s clinic was running 60 minutes late.

I froze.

There’s a fucking surprise, I thought. There are probably people in here who were behind my husband in the queue 15 months ago and are only just being seen. Three out of four of them will be dead by this time next year, I realised. I looked around and wondered which ones.

The same staff, the same waiting time, the same room, the same chairs, but no husband. No husband at all, because they couldn’t save him, here in the best place.

My husband’s oncologist never actually came to say goodbye. He never shook him by the hand, or said that it had been a pleasure to treat him. One of his colleagues discharged him in the end, because it was late on a Friday night and everyone else had gone home. We never saw the oncologist again, until the other day when I bumped into him as I was walking into Radiotherapy, and he was wandering over to speak to a patient.

He was thrilled to see me. He summoned over the whole team who were all smiles and welcomes and full of words about how sorry they were to have seen on the news that my husband had passed away – he was such a lovely man, they said. So humble. We’d had no idea how incredible a career he’d had, they said. Nor did we, I thought.

Then, of course, at the sudden realisation that I was quite clearly now a patient, the joy turned to concern. They wanted to know if I’d be OK. The oncologist asked after the boys. One of the nurses ran off to find catering quantities of tissues, and shoved sheet after sheet into my hands as the tears came – just as they always did, for my husband and me, every time we mentioned our darling boys as we sat together, holding hands, in the room just steps away from where I stood again, on my own.

They hadn’t forgotten us. It made me feel validated again. I was a human being – not a patient – and, more to the point, so was my husband. Of course they’d wanted to save him. They wanted to save everyone – and for the people like us with young kids, they throw as much as they can at us, even when they know there’s barely a scrap of hope. A scrap is sometimes enough. I think I understand that now.

I looked around, and realised that there would have been a string of patients who’d died under the oncologist’s care since my husband was discharged. The corridor still buzzed with people walking up and down; some in hats, some with lanyards, some in uniforms. A woman pushed her husband, too frail to walk, in a wheelchair. I looked at her sympathetically – I’d been there, even though my husband never opted for a wheelchair if he had the strength to walk. I realised she was looking back at me with sympathy too; I’d forgotten that I was now quite obviously a cancer patient, not a carer. Her husband had probably been normal and healthy, when mine was the patient in that wheelchair, just over a year ago. She smiled a smile of cancer solidarity, which implied that she knew how I felt. You haven’t a fucking clue, I thought. You poor, poor woman. Just you wait.

I realised then, that I’d been carrying so much anger within me for the team who couldn’t make my husband better, even though it wasn’t their fault. They can’t possibly shake every patient by the hand when they send them away to die, or point their relatives towards the BEREAVEMENT SUITE, because they’d be doing it every day. It would be soul-destroying. But, they did remember us. My husband was someone to them; they liked him, and they did their best. Sadly, it wasn’t enough, but it wasn’t because they hadn’t tried. They tried everything. In fact, they probably tried too much – and my husband had wanted them to. Anything for another few precious days with his family.

Maybe, I didn’t just need this wound to scab over. The act of coming back here – of ripping it off, letting the blood flow out, and starting again, is perhaps just what I needed to do to let the healing process start afresh. It’s been a bloody long and complicated way of healing, though.

Just because my husband’s time at the cancer hospital ended, doesn’t mean that time stopped here for everyone else. The place still functions and runs without him, even if the home I return to doesn’t function anywhere near as well.

Wives still push dying husbands up corridors. Bald little children with tubes in their noses still walk into the garden to sit and read for a bit, and try to be children. Women with hats and drawn-on eyebrows still complain about the shit coffee, but buy it anyway.
 

And the lucky ones get to walk past the door of that fucking BEREAVEMENT SUITE on the way out, and keep on walking.

Love Fanny x

A Picture of Denial.

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.

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