Injecting a note of caution

Those reading this blog who have prostate cancer and are on hormone therapy will know that the spring-loaded needle that drives the hormone implant into the luckless victim’s abdomen can sting a little. My last injection was administered by a doctor with the skill set of a porcupine in a hurry. In our house he’s now known as the South Lambeth Road Slasher (SLRS). For him it’s not so much an injection; more a drive-by shooting.

With my next injection due, I called the GP’s surgery to book an appointment with the nurse rather than a doctor and told them to make sure the Zoladex implant needle was in stock. Turning up two days later I tapped my details into the computer on the reception desk and guess who I was down to see? Yes of course, the Slasher himself.

I gently suggested to the lady on the desk that I didn’t want to waste the doctor’s time and would be very happy to see a nurse; only to be told that there was no nurse on duty. Finally, I had to admit that I didn’t have full confidence in the SLRS and asked if I could have an appointment with someone else on Monday or Tuesday. This didn’t prove possible at which point the lady on the desk volunteered to come in and hold my hand.

After agonising over the potential agony, I agreed to let the Slasher do his dirty work and waited for him to come and call me through. When he appeared, I gave a big wink to the ladies on the desk, all three were now in on it, and they burst into laughter. Hearing this the doctor said ‘I guess everyone’s so happy because it’s Friday’ which made everyone laugh some more.

This is where the story doesn’t build to a jabbing climax as It soon became apparent the pharmacy hadn’t delivered the hormone bazooka and I was able to escape unharmed from the clutches of the evil genius.

Unfortunately, I’ve just checked my voicemail and I’m now booked to see the Slasher on Tuesday. Will I escape unharmed, will I bottle out, will some kindly nurse come to my rescue and will this story ever get to the point? Stay tuned.

Slasher update

Pitching up at my GP’s surgery on Tuesday at 10.30, I tap my details into the reception desk computer and am rewarded with great news. The Slasher has been left on the bench and I’m seeing Nurse Angela for my hormone injection.

A shout of joy (mine) wakes up a couple of the older patients who are asleep in the waiting room’s heat. They look vaguely irritated, wonder what’s going on, but are soon back catching flies. So, it’s big news, the Slasher is side-lined.

Nurse Angela has been at the surgery for years and while she’s never skewered me with a Zoladex shot before, I’m mightily relieved it’s her doing the skewering and not you-know-who.

Because it’s a fairly serious procedure and being the professional she is, Angela wants a doctor in the room. A young medic enters, and I suppose out of professional courtesy she asks the doctor if he wants to give the injection. As you can imagine I’m having none of it and make it very clear if anyone’s going to ram a needle into Jim’s abdomen on the 15th January 2019 then that rammer is Angela.

The doctor steps back and Angela asks me how long I think she’s been giving injections. I hazard a guess and say two weeks. She laughs and says actually it’s 45 years.

The needle is unleashed, explodes into my belly with almost no pain whatsoever. My next shot is 9th April. I’ll be booking Angela early to avoid disappointment.

Practise Nurse

Having read the original article, Marnie, a practise nurse, got in touch. She has some interesting insights:

‘Although this injection (Zoladex) is fairly standard, originally nurses were not allowed to do it, only a doctor and back then they used to use a local anaesthetic. Over time nurses became deemed competent to do it, so that job is generally handed down. Research also shows that the local anaesthetic causes more problems than it solves so we stopped using it quite some time ago.

As with any task we do, we get better the more we do it, even in a very large surgery there may only be 2-3 patients on it at any one time so our skills can get a little ‘rusty’.

Because of this it is often left to one person only for these appointments, so they can keep their skills polished up. The drawback is, this treatment should not be delayed and if a (member of) staff is off sick, or (has) left, someone else should take over to make sure it is given on time. A new nurse or locum may not yet be trained to do it, so it is down to ‘slasher’ as a temporary solution.

I give my patients the choice of standing/sitting/laying down when they have it, sometimes a different position may help reduce the pain. I have even over the years had the odd patient who learned to do it themselves, rare but if you are brave enough!!’

This reminded me that the very first hormone injection I had was at Guy’s Cancer Centre where the nurse gave me a pain free shot standing up. I’ve suggested this to other nurses and doctors who’ve looked at me like I was mad.

Unfortunately, Marnie is also a cancer patient and is waiting on scans to see if her treatment has worked. Thanks for getting in touch Marnie and I sure hope it has.


 

I’m making a list, I’m checking it twice

Technically I was tidying but really I was rummaging through a cluttered cupboard in my home office. I like to think of this as my man-cave but in a small house in central London it’s more like a man-cupboard. The rummage produced a list. Now to he clear, I like lists – a lot because:

  1. They help me keep on top of work.
  2. Stop me forgetting things.
  3. And allow me the joy of putting a little tick next to a completed job.
  4. Some people cross things out once they’ve completed a job but that carries a huge risk of not being able to see what you’ve done. No serious list maker would stand for that.

Christmas is the time of year when lists come into their own, with Santa’s Naughty & Nice list setting the Gold Standard, though to be fair to the fat, bearded chap I check my lists a great deal more than twice.

Inevitably, given the nature of this blog, the list I’m talking about is a little less full of festive fun. Prior to my prostate cancer diagnosis, I’d spotted blood in my urine which prompted me to go to the doc and set me off on my cancer capers.

What I’ve not mentioned before is that two years earlier I had also been peeing a small amount of blood and had sought medical help. On that occasion, following various tests, I was given the all clear though not surprisingly the question: ‘did they miss something?’ has popped into my mind on more than one occasion.

Which brings me to my uncovered list which were the notes I took at the time during a consult with a urologist at Guy’s Hospital.

  1. Benign cyst on left kidney.
  2. Enlarged Prostate. May cause problems in later life.
  3. No sign of tumour or cancer.
  4. Blood (in urine) probably caused by prostate.
  5. CT scan of kidney in case ultrasound had missed anything, ruled out cancer.
  6. Blood should go away, can take drugs for prostate, but these can have side effects.
  7. CT scan 3rd September at St Thomas’ Hospital.

So, what to make of that? Well I’m certainly no doctor, but it looks like they did all the analysis necessary though of course the enlarged prostate is the giveaway. I love the idea that it ‘might cause problems in later life’. I’m pretty sure I had in mind when I was 80 or 90 not just two years down the track. Unfortunately, it looks like the Unwelcome Guest had already made a booking.

I suppose if I have a criticism it is that I should have been put on what is called Active Surveillance and monitored more closely.

I’d forgotten I’d had the CT scan on 3rd September which is my birthday, but remember feeling deliriously happy when I saw the urologist for the last time and was given the good news.

Two years later after I’d started again on the unlovely round of tests, I remember telling Mrs Preen I had a strong conviction there would be no free pass this time. Unfortunately, I was right.

But let’s keep the doom and gloom at bay at this time of year. I’m feeling fine and the radiotherapy side effect, needing to pee all the time, is gradually going away which means I’m sleeping more and feel less tired.

Given the nature of this post, I guess I’ve got to finish with a list, so I’d like to shower seasonal goodwill on all of the following:

  • Those who have their own Unwelcome Guest.
  • Loved ones of those who do.
  • Friends and family who worry about me.
  • And anyone else who’s along for the ride.

Happy Christmas, Happy Holidays and Happy New Year. I’ll be back at the start of our next solar orbit.


The year of living cancerously

It’s now almost exactly a year since I discovered the Unwelcome Guest had set up shop in my prostate. The presumptuous little bastard.

To celebrate, and I’m going for gold in the most inappropriate use of an English word, I thought I’d look back on my year of living cancerously; not so much at the treatment and side-effects but rather at what it does to your life. SPOILER ALERT: It’s not all depressing.

One in two people in the UK will develop cancer at some point so to some degree it’s a shadow that hangs over us all but make no mistake there is a significant difference between a potential threat and the real deal. If you become a member of the cancer club, the club that nobody wants to join, it packs a punch. When the doctor looked at my scan and I got my first glimpse of the Guest, I broke into a sweat, felt faint and thought I’d collapse but lay down and gathered myself. I cried when Mrs Preen and I parted at the tube station.

Take the following thoughts and questions, mix them in a blender, and you’ll get a sense of how it feels in the first few days: What is a PSA test? How much is the biopsy going to hurt? Will I be here next year? What do I tell my 15-year-old daughter? What’s a Gleason score? Why me you bastard? For best effect have these going around your head at three in the morning while working up a muck sweat of worry.

Catch cancer early and you have a decent chance of survival. Fortunately my cancer was mostly contained within my prostate with the Guest just nudging one lymph node. When AA Gill was diagnosed with terminal lung cancer, he described himself as having the Full English. Mine is more of a continental breakfast, but no one should ever get complacent; what was once a croissant can soon become a fry-up.

In 2008 PJ O’Rourke was diagnosed with a treatable form of cancer. He quipped: “I looked death in the face. All right, I didn’t. I glimpsed him in a crowd.” I guess the same goes for me. I once got drunk with PJ in Mogadishu when we were both there working for ABC News. We quoted Auden and Yeats at each other, pretentious little pricks, but I’m happy to say he’s still very much alive.

Pretty much at the outset I was given a 50/50 chance of my cancer being cured and if not cured, was told it had the potential to be managed successfully for a number of years. Dan, a fellow blogger, and prostate cancer patient has a warning: ‘Once you introduce the word cancer into your vocabulary, it never goes away, even if the disease does. There will always be that little cloud called “fear of recurrence” that will follow you around for the rest of your days’.

Perhaps its superstition or perhaps it’s just good sense but Dan’s wary of ever saying one is cured or cancer free. Maybe it’s like being an alcoholic, you are only ever a recovering alcoholic even if you haven’t had a drink in 30 years. He likes the acronym NED, ‘no evidence of disease.’ Saying you’re cured is dangerous; you may think you’re done with cancer, but cancer may not be done with you.

I follow a Facebook page ‘Prostate Cancer UK Support Group’ where others with their own Unwelcome Guests post their stories, conditions and questions. Many are poignant, funny and some unbelievably sad. I’ve seen posts detailing men who are diagnosed while still in their forties and early fifties, which seems so unbelievably unfair. Many also find the treatments that I’m on such as hormone therapy and radiotherapy almost unendurable. While everyone’s treatment will differ so will their reaction to the treatments and side-effects.

But of course it’s not just the patient who has to live with cancer, his family are also on the same unwelcome journey. Right from the outset I took the decision to be upbeat and to make the journey as bearable for them as I could.

Yesterday Mrs Preen and I took the dog for a longish walk in the countryside and I asked what it was like to be married to a husband who was foolish enough to develop prostate cancer. Her answer came in two equally surprising parts. First, she said she was worried she didn’t worry enough about me! Not, she was quick to reassure me, because she didn’t care but because she was convinced all would be well. She said that if on balance I’d like her to worry more she would get right down to it.

I’ve mentioned this before elsewhere, but she said she continues to be astonished at how remarkably upbeat I am most days and actually less grumpy than prior to my diagnosis. I guess all wives can use a less grumpy husband, but why this should happen after contracting cancer seems to defy logic. But you know what? I’m not going to dig too deeply into the whys and wherefores and just be happy that’s the case. There’s plenty of time to be miserable should the Unwelcome Guest decide to go medieval on me.

And what of my teenage daughter, what are her thoughts? She knows I have cancer, but I rarely mention my condition or treatments. I’ve done this to protect her, but it occurred to me that my cancer might be seen as off limits; something that shouldn’t be mentioned. What could be worse than fretting about something you can’t talk about? So, we had a chat about it and apparently her mother had told her that dad wasn’t going to die anytime soon and that had offered enough reassurance. At 15 there’s lots of other stuff going on and heaven knows I don’t want to be a worry when the spectre of GCSEs is causing enough terror all by itself.

When you tell people you have cancer, they don’t say it, but their first thought is, he’s going to die soon. That’s a reasonable assumption because that’s exactly what I thought when I was first diagnosed. I’ve got a pretty good shot at traveling on a few more years but I don’t know for sure where I’m headed and at some point, it might not be in a very desirable direction. Then I reserve the right to be less cheerful. But right now what cancer gives me is all the encouragement I need to live in the moment. When I was young the future was like a huge jigsaw puzzle that I’d construct when I finally got around to it. At almost 65 and living with cancer, the future is now.


Radio Days (13): Last Blast

On Wednesday of this week at 9.15am my prostate was blasted for the last time. My 39 rides on the doughnut of doom are complete and hopefully the Unwelcome Guest has been given all the encouragement he needs to fuck off.

But the doughnut wasn’t going to give up without a struggle. On Tuesday I was attending a work conference and sat on a panel dispensing words and wisdom and a couple of laughs on the stuff I do for a living. Talking in public meant my phone was switched off so I missed a call from St Thom’s radiotherapy department telling me the doughnut was busted and my final treatment might be delayed. So close to the finishing line and now this. I called RT, but nobody picked up, so I left it until first thing Wednesday, but then the number was constantly engaged. As regular blog followers will know my RT treatment has by no means been bad, but I really wanted it over.

Also I’ve made friends in the waiting room of doom and wanted to say a fond farewell to certain members of the early morning cancer crew.

Mulling over what to do I decided to head out as usual to St Thom’s even if I had to wait all day for the doughnut to be fixed. A friend of mine recently asked if my experience had put me off eating doughnuts. To which my answer is, if any reader wants to send over a box of Krispy Kremes, they won’t go to waste.

Arriving at St Thom’s it was just Aaron, ace radiographer, and me. He was on the phone but gave me the thumbs up to say the doughnut was in peak condition and ready to give Preen one last ride. Slowly, other RT technocrats started assembling and I started drinking my 350ml of water.

Alan and Peter, two of the cancer crew, arrived as they’d not heard the doughnut was broken, so I was delighted to be able to say goodbye to them and wish them well. It was Peter’s last blast too but unfortunately Alan still has around 12 fractions to go.

So there we are drinking our water and gabbing away as we do every morning. Unfortunately, it takes a while for me to be called through so when I’m lying in the doughnut I’m absolutely bursting for a pee, but it’s going to take an earthquake to stop me seeing this through and anyway it seemed disrespectful to piss all over the doughnut which has been doing so much to see off the Guest. Treatment complete I slide out of the doughnut, get my picture taken and leg it to the toilet. Doughnut done and dusted.

Friends have been so kind sending me jovial upbeat messages, Sarah & Tim sent a bottle of bubbly and I bought myself a litre of Jack, so I may not be quite so sober as I have been for the last two months.

All that remains is for me to thank the radio stars who have administered my treatment with caring professionalism and not a little humour. The NHS is blessed to have: Naeema, Rafiq, Helen, Damon, Orla, Georgia, Aaron, Eileen, Catherine, Hodma and Sharan.

Nothing now happens until January when I take a blood test to check my PSA level and talk with the oncologist about the next moves to keep the Unwelcome Guest off my back, not to mention my prostate. I plan to enjoy Christmas and put Jim’s cancer capers to the back of my mind.


Radio Days (12): Light at the end of the doughnut

With thirty-six rides on the doughnut of doom complete, there are only three more to go. By 10am next Wednesday my radiotherapy treatment will be complete; there’s light at the end of the doughnut.

Today Mrs Preen and I attended my final treatment review session with Maggie who seemed pleased with my progress. Not much has changed as far as side-effects go, though at night I’m wearing out the carpet on the way to the loo slightly more frequently. About three weeks ago this was getting to be quite a drag and lack of sleep was making me feel as tired as a teddy bear. It’s amazing how the body can adjust, because now, even though bog attendance has increased, once back in bed I generally go straight back to sleep. Feeling more rested, I managed to stay up until 10.30 last night; so rock & roll.

Maggie warned that for a week to ten days after treatment the side-effects may get a little worse but by strength of will and force of character, I’ve decided that’s not going to happen to me. Let’s see who wins, me or the doughnut.

For anyone reading this who’s about to start RT all I can say is that it wasn’t so bad though of course everyone’s experience differs. Alan, one of the early morning cancer crew, has found sleeping very difficult as he’s trudging to the loo on the hour every hour. The poor guy looks tuckered out.

I’ll be glad not to have to slog to hospital every morning, but the bicycling has kept me fit and I’ve continued to work throughout, though perhaps not quite at full speed. (Don’t tell the boss)

On our way out the door Maggie handed me a sheet detailing support group meetings for prostate cancer patients. At the end of every month there’s an event called Prostate Life! (their exclamation mark, not mine) where guest speakers are invited to talk on subjects ranging from ‘Prostate Cancer – what is it?’ to ‘Psychological issues and managing stress’. Interesting stuff and no doubt you’ll want me to put your name on the door, but the one I’ve got my eye on is The Festive Meeting on 28th December. Obviously, I’ll be wearing my Christmas jumper, but what does one take to a festive prostate cancer meeting? Frankly the mind boggles.


 

Radio Days (11): My side-effects have side-effects

Most days the dog and I trot round to Kennington Park. It’s particularly beautiful at the moment with the leaves on the London Planes turning to shades of gold and brown. Rusty, being gold-leaf coloured, disappears as if she’s wearing camouflage.

I remember taking this walk just over a year ago, not long after the mutt came from Battersea to share our life. It was a scary time, I’d just been diagnosed with prostate cancer and I had no idea what the future held. I wasn’t even sure I had a future.

Things have changed for the better and I have every reason to believe Bucket and I will be taking the same stroll next year. But I know from interaction with others that the early days, just after diagnosis are tricky. My life felt out of control; slipping from my grip.

I’m currently having two day’s grace from Radiotherapy while the doo-dat is jacked up and serviced. I want it over but can’t deny it’s quite pleasant to get some time off.

I’ve had 26 rides in the doughnut of doom and have a further 13 to complete the course. I asked Aaron, one of the radiographers, how many patients he treats in a day and he told me it’s between thirty and forty. That’s a lot of prostates getting clobbered by just one machine.

Sorry to bang on about the side-effects of radiotherapy yet again, but something needs to be made clear. I was warned that about a month in many people feel overcome with tiredness and fatigue. I’m feeling a little tired myself for the simple reason that I’m now getting up to pee four times a night. I’m wearing out the Axminster on the way to the bathroom. I’d assumed fatigue would be a direct product of the treatment rather than a side-effect of the side-effects. Breaking News: Man feels sleepy because he’s not sleeping very well.

I’m now scanning the internet to find side-effect free medication that’ll stop me talking about sodding side-effects.

Moving right along, I want to introduce you to a new member of the early morning cancer crew, another of us lads (Lads! Who are we kidding?) who sit waiting for our doughnut appointment. I’m calling him Stringbean and I thought to shake things up, I’d tell his story in the style of Damon Runyon.

Such a guy as wears shorts

So it’s round 9 bells and we’re all sitting in the paddock, waiting for one of the radio jockeys to come in saying, quite formal: ‘Please start drinking Mr Preen’ on account of we need to get outside of a jug of water to fill our bladders, so the ray guns are hitting their target. And there are the usual jokes like ‘I’m having a little whiskey with my water today’, which aren’t funny but hey some of us like a little whiskey now we have cancer an’ all.

We are a gabby bunch talking of this and that with someone crying the blues about Radiotherapy, Hormone-therapy Tomotherapy and Brachytherapy until most of us are wondering if there’s some kind of therapy that’ll put a sock in his mouth.

Just then a new guy busts in. So of course we give him the big hello, nice to see you, haven’t seen you before and so on. He’s a tall string bean of a guy, maybe seventy with white hair and not so remarkable except he’s wearing shorts, a t-shirt and trainers. We’re all thinking, who is this wingnut wearing beach clothes in the middle of autumn? Of course, being English we stay shtum and Stringbean sits down and we lapse into silence and wait our turn on the doughnut.

Next day we’re there shooting the breeze when in comes Stringbean once again sporting the shorts, t-shirt and trainers rig. This is too much for me so I’m saying: What’s with this garb? Are you jogging here? No Stringbean says, I’m coming from Bromley and taking a train and a bus. And I say you must be some kind of chump, it’s freezing out there.

What you say is true, he says, but a story goes with it. Well of course we all love a story and are all ears, even those of us who don’t hear so good no more.

Stringbean starts and it sounds like he’s crying the blues along with Mr Therapy. I’m working hard all my life, he says, and sometimes I’m on Easy Street and have plenty of scratch and other times no scratch at all, maybe not even two bobs to rub together. One time a dame gives me the run-out powder and I’m sad as all get out.

And all us greybeards are going: tell me about it, been there done that, because we’re thinking we are great sages about life and very likely had the same ups and downs ourselves. Though of course young people are claiming we know nothing at all and maybe not even that much, which is very fair because that’s how we think about them.

Stringbean continues: A couple of years ago I retire from my job in the government department and by now I have a few bobs to my name, a little pension income every month and life is very sweet. And one day I’m waking up and not running for the 6.15 train when suddenly it hits me: I’m on holiday for the rest of my life! And now I’m such a guy as wears holiday clothes 24/7.

Well this sounds fine to one and all except we live in England where the temperature is lower than a limbo dancer and he’ll be lucky not to get chilblains to go along with his prostate cancer, but of course we keep that to ourselves.


Hormone Therapy: Is there a good side-effect?

I’ve been undergoing hormone therapy for nearly a year and have just had another injection or implant. These last three months and stop hormone testosterone from reaching the prostate cancer cells. Unfortunately cancer relishes and grows on a diet of testosterone.

In previous blogs I’ve talked about the various downsides to this form of therapy, particularly the unpleasant side-effects. In a moment I want to talk about the possibility of an unexpected upside. But first let’s look at the sharp end of this treatment; specifically a bloody great needle.

A little prick

Those of a squeamish nature may want to look away now. The injection is delivered by a spring-loaded needle that shoots a slow release capsule into one’s abdomen. I’m not queasy about jabs but I tend not to look too closely as this medieval instrument of torture.

If the medical practitioner delivering the shot is skilful, it’s a moment of mild pain. If the skill level is one notch down, it does hurt a bit. If the doctor, and I use the term advisedly, has the chops of a butcher then the pain level is not inconsiderable.

My first injection was at Guy’s Cancer Clinic where a supremely skilled nurse popped it in, no problem. The nurse at my GP’s surgery is a little hit and miss and last time there was a fair bit of bruising. This time I was told a nurse was not available and a doctor was going to do the honours. Everyone knows doctors are useless at delivering jabs as they do it so infrequently and it’s a job best left to nurses who do it all the time. So I want to tell you that on this occasion I couldn’t have been more wrong, and the doctor delivered the injection in a professional pain free manner. I want to tell you that, but I can’t. For the first time I actually shouted out in agony. I can’t imagine what the other patients thought was going on.

Prostate cancer is tracked in various ways but the most common and widely used method is a PSA test that measures the total amount of prostate specific antigen (PSA) in your blood. It’s normal for a man to have a small amount of PSA, but a raised PSA level might indicate that further investigation is needed. When I was first diagnosed my PSA level was 5.03, which is relatively low and might not even indicate cancer. However, a physical examination and biopsy showed the Unwelcome Guest had set up shop.

Just a month after having my fist hormone injection my PSA was down to 2.61 and then six months later it was down further still to 0.8. So clearly the therapy is working and there is every expectation that when I have another PSA test in January of next year it will be even lower.

Last Friday Mrs Preen and I attended a radiotherapy treatment review session with Jenna the Urology Advanced Practitioner who we’ve met before. As ever she is excellent and a credit to the NHS. The bad news is she’s leaving to go work with one of the radiotherapy manufacturers, where I’m sure she’ll do a great job, get paid far more, but will be a great loss to our care service.

I have an appointment with my oncologist – still one of my least favourite sentences in the English language – in January. I asked whether, along with the PSA test, I’d have another MRI scan to take a closer look at the Unwelcome Guest, but Jenna said I won’t because there will be nothing to see, the cancer will have gone. I’m fully aware the Guest can make an unwelcome return, but I hadn’t appreciated that once the radiotherapy is complete, the current incumbent will have been booted out.

The docs then monitor my condition using a PSA test every three months until June and then every six months after that. If subsequent tests produce a similar result to that taken in January, then all is well. If the PSA level starts to rise, then that is a cause for concern.

I have another two years of hormone therapy in front of me and sure wouldn’t mind having my sentence reduced. Gabbing with one of the cancer crew in the waiting room, one of my fellow sufferers said some recent research indicated that 18 months hormone therapy might be sufficient. I put this to Jenna, who merely said I should ask the oncologist in January, but this got me thinking.

An unexpected upside?

Regular readers of the blog will know that despite having cancer I feel remarkably spry and chipper; I’m not depressed or downhearted. Some comment on how ‘brave’ I am and wonder how I continue to be so upbeat. Trust me I’m not brave and neither am I putting on a brave face. Most of the time I really do feel happy. If I didn’t I’d say so.

Here’s another thing: Whenever food is served in our house, Mrs Preen and the daughter laugh at me as I’m always the first to say how delicious it tastes. For the absence of doubt, we are both good cooks.

At the back end of last year when this whole cancer farrago kicked off and it was decided that instead of having my prostate removed I should go down the hormone and radiotherapy route the oncologist outlined its pros and cons and talked about the possible side-effects. She then made a throwaway remark, claiming one of her patients had once told her he’d never felt better than while on hormone therapy. At which I remember thinking at the time: yeah right pull the other one. Typical doc just trying to gee me up and make me feel better.

So here’s the inevitable question: Is the reason I’m feeling happy and content and food tastes so good a completely unexpected side-effect of hormone therapy? Am I enjoying some form of chemically induced euphoria which will come crashing down once the therapy finishes?


 

Radio Days (10): Half-time

Tomorrow the seasaw tips and I start on the second half of my radiotherapy treatment. Just 19 fractions to go and then the doughnut and I part company.

Many of my prostate pals have already done their time: Bassie and Chas have gone, and John has one session left. Unfortunately their places are quickly taken as prostate cancer seems all the rage these days.

The many new faces include Sir Alan, a transatlantic sailor and board-level businessman. He’s now in his 80s but sailed to the Caribbean and back when he was 65 and was messing about on his boat in the Solent last weekend.

As you can see from the picture I finally got one of the doughnut jockeys to take a snap of my insides. These are the screens they look at while I’m being nuked.

They take pictures of a series of slices through the abdomen. The white sections on either side are my hip bones and the central section is my prostate and bladder. I think the red circle indicates the prostate and the flattened orange circle is a lymph node. This has to be zapped as the cancer has set up camp there.

Lymph nodes and lymph vessels form a superhighway that allow fluids to be transported around the body. Unfortunately cancer likes to hitch a ride on this highway and uses it to spread, hence the need to take out this particular node.

Personally I don’t think I’ve ever looked lovelier than in the picture below, but the prostate shows clearly in blue. Just above that keen sailors will have spotted three tabs marked Pitch, Roll and Yaw, all rated at zero. So clearly the radio-waves I was surfacing barely ruffled the surface.

Prostate Cancer

If anyone has anything to add and can decode these pictures better than I, then please do so.

Cancer communication

Sometimes people talk about cancer in unhelpful ways. In newspapers a celebrity is said to be ‘battling cancer’ and if they die they’ll have ‘lost the fight’.

At times it’s suggested cancer can be beaten if only people try hard enough. I know why newspapers do this because it plays to the emotions, but it in no way reflects what it’s like to be a cancer sufferer. When people succumb to the disease, suggesting they’ve lost a fight or didn’t try hard enough to overcome it is odious.

My approach is to treat cancer with the contempt it deserves. I cycle to my hospital appointments and go to the gym twice a week ostensibly to keep healthy, but actually it’s my way of saying you’re not going to stop me living my life buster. Or else I just laugh at it and hope it feels ashamed of itself.

Of course I’m aware it may be the Unwelcome Guest who has the last laugh, but when a person dies, the cancer goes too. Deeply unsatisfactory for the host and presumably the Guest.

Radio Days (9): The early shift

Leaving the hospital on Friday I cycled through The Cut at Waterloo and spotted an art deco antique shop called Radio Days. Well, I had to stop and take a picture for the blog. Thirteen RT treatments done, twenty six to go.

Radiotherapy
Early Morning Shift

I want to introduce you to members of the St Thom’s Cancer Club (early morning shift). These are the guys I meet every day at around 8 o’clock as we sip water waiting for our treatment slot.

From left to right we are: Muggins, Bassie, John and Charles. We come in early as we all work full-time jobs. They are a cheery bunch, we have a good natter, and I always look forward to seeing them.

Bassie is a business consultant who helps start-ups write their business plans and secure finance. John, with his pleasant Irish brogue, is a security guard at a bank in Canary Wharf and Charles, or Chas, is a mechanic who has his own garage and a passion for MGBs. Both John and Chas are coming towards the end of their treatment. I’ll be sorry not to see them but interested to find who takes their place. Cancer, that most democratic of diseases, means I meet folks from all walks of life who I’d never normally come across. So who says cancer is all bad? Well me and everyone else who’s got it obviously, but more of that in a moment.

Way out

St Thomas' Hospital

We are such creatures of habit. The early crew all sit in the same seats every day.  I face Chas, while Bassie sits to his right and John is positioned a few chairs away to my left. Controversially (such a rebel) I sat in a completely different seat on Friday and so for the first time noticed the ‘Alice in Wonderland’ sign that hangs at the back of the waiting room. What the hell is a Superficial Way Out? I don’t want some back of a fag packet way out, I want one that’s profound and sincere. Typical NHS can’t even fund proper exits.

Doughnut pain

In Radio Days (8) I mentioned the bladder discomfort I’d endured while inside the doughnut and was worried it might happen again. I managed to grab a few moments with Maria who looks after my treatment review and reassuringly, she thought my bladder might have been overly full or had some kind of spasm but was very unlikely to be a product of the treatment on the day. Her only concern was whether I felt fine after I’d had a pee. I did and so far, it hasn’t happened again.

Tough love

Reading posts on the Prostate Cancer UK Support Group I see many people suffer side-effects induced by hormone therapy. They talk about mood swings and heightened emotions with people fine one minute and crying the next.

I too am on hormone therapy, which has some unfortunate side-effects: hot flushes and disturbed sleep, but in general I feel happy and optimistic.

A month ago Mrs Preen called me out for being a bit moody. Being a man and therefore having no self-awareness, I resolved to monitor my temperament.

Long before I got cancer, but when I was having a right old moan (hey I’m 60), she’d call me an old goat. Tough love in the Preen household.

Today after reading posts about mood swings and irritable behaviour I asked her how I was doing and whether I was exhibiting more goat-like tendencies than usual.

First, she asked if I wept quietly when alone. I don’t. Then came this: I’m astonished how cheerful you seem and are greatly improved! All of which left me smiling, but bewildered. Cancer, whatever next?


 

Radio Days (7): Breakdown

Don’t worry it’s the machine not me. Mrs Preen and I walk into St Thom’s at 8.30 sharp for my Treatment Review and it’s clear something is up. Apparently, when the first radiographer arrived at 7.30 to crank up the Tomotherapy do-dat, the machine was having no part of it and refused to be cranked. More of this in a moment.

My Treatment Review is with Maggie whose beat is normally at Guy’s Cancer Centre, but she is filling in for Jenna who assiduous readers will recall from Radio Days (1).

As mentioned last time, this is not to see if the treatment is working but to check how I’m doing and whether I’m experiencing debilitating side effects. I tell her, I’m fine but do have to get up to go to the loo a couple of times a night and no longer pee with the intensity of Niagara Falls. But hey if this is what it takes to eject the Unwelcome Guest, then call me satisfied. Maggie is content with my progress, so Mrs Preen and I amble back to the waiting room to discover there’s going to be a lot of it, waiting that is.

With the Tomotherapy machine on the blink, we sit expectantly for the engineer to arrive from Guy’s to jack it up and give the thing a new set of points and plugs. News starts to filter through: The engineer is on his way (hurray!), but he’s stuck in traffic (Nooo!) and then I see a bloke who might be the engineer, though to be fair he looks more like an electrician. Are you the engineer? I ask, no I’m an electrician he says and shows me his mulitmeter.

I turn to Orla, a chatty Irish colleen and ace radiographer, who explains the RT machine detests being powered down completely, but a mains outage has done just that. The machine is furious and will not tolerate being treated in this cavalier manner. Questions circulate: Has the electrician got his little pack of fuse wire with him? Has anyone used fuse wire since the 1970s? So many questions but still no engineer.

We hear a faint rumbling noise: Power is restored! But the machine is still in a strop. Bits of equipment are trundled by and then suddenly a man with a laptop computer appears. It’s the engineer, he is amongst us. Tenderly, he brings the machine’s system back up, it is placated and consents to start lasering the waiting patients, who have been waiting patiently. Finally it’s my turn, I’m irradiated fit to bust and I’m on my way out at just after one o’clock. This is the first road block in an otherwise seamless treatment schedule. And now I get the weekend off and maybe a couple of glasses of wine to boot. Life is sweet.