Monday, 24 August 2026

PUMP PHASE

 THE DEATH SUITE 9: PUMP PHASE


This was my third experience of chemotherapy, and the first two were more tolerable than I had expected. Was I going to miss out on the chance to write about a more full-on version? It turned out not… The chemo ran from October 2025 - April 2026, over 11 cycles - 12 were planned, but the last was cancelled following my hospitalisation after Cycle 11, when doctors judged that the severity of the side-effects outweighed any further benefits. 


CYCLE 1



Someone offered me a seat on the tube today

First time ever.

Was it the age or the cancer?

I'm pretending it was my two big bags...


That's me, as reflected in the angled outer metal of Maggie's cancer support centre, Southampton.



Looking at it positively

this is the most efficient use

of our cancer table

since 2023…

  


Ten poos today!

Must be another positive:

my system working soft as poss

to flush out a passing enemy.

   


I'm not against death

I see the necessity,

so it seems a bit rich

if I plead a special case.

 


And what's the point

I might have asked, however long, of life itself?

But that gets a little grand:

I've only got four lines.




With a PICC line in place

the nurses say I must serve underarm -

my tennis reflecting

how cancer alters the game of life.


 

Chemo is pleasant

Four hours hooked up in quiet

with regular drinks and no distractions.

Were it not for the effects… 


Four poos per day’s

been my average now for eight months.

Have I missed my big chance

to make a thousand-image archive?


        

Why, today, do I think of death?

Same reason, I guess,

as every other day -

and yet, in a way, I think nothing of it.

 

First line combinwa the last two lines of James Schuyler’s poem ‘Labor Day’, 1974

 


My plan is simple -

live

until I die…

If you can call the unavoidable a ‘plan’.

       


Which tumour’s going to kill me?

may be my most macabre question.

Bowel, lung, mesentery or liver?

And does the difference matter?

 

CYCLE 2



Ha!

My first blood test with a PICC line in place

and the queue is an hour!

I switch to the wait-free needle-in-vein.

 

It’s a differently-staffed procedure to extract blood from a PICC line, and there were three nurses for the needle, one for the PICC line, and a considerable imbalance of demand


       


My new sleep buddy

is a pump.

But Steph can hardly be jealous

It’s only twice a fortnight.


       

‘I’m happy’, I tell the senior nurse when she asks for feedback

‘that you’ve kept me alive to answer that’.

That’s my schtick and I’m sticking to it

until it’s not true.


      

Three days with the pump each fortnightly cycle

Three others with appointments.

Four too coshed to do much.

I’d better make the most of the other four!


                         

How can death be seen as bad?

A non-experience

with no ‘me’ to not-have it anyway.

All the same…


See, for example, Thomas Nagel: ‘Death’ in the philosophy journal Nous IV, no. 1, 1970. That's the PICC protector used when taking a shower.


       

I have this mental picture of myself

as a vigorous young man…

Aged 67,

dying of cancer.




Who wants immortality?

The Greenland shark can live five hundred years or more,

slowly-slowly down in the deep.

Sounds like a reasonable compromise. 



It seems odd to be afraid

of replacing all your problems

with one that solves itself

in an instant.



How do I fancy it?

Should I slip away, pass on, join the choir invisible?

Leave the voting list, switch to counting worms?

Cash in my chips, turn turtle, or just go Father Ted?


     


All my food

is fast these days:

not so much arriving

as departing.


      

No-one ever asks me

if I’m going to die.

It’s as if they’re afraid

of hearing a spoiler.       


CYCLE 3




Ah, my hair

is thinning!

Real chemo’s here –

 at last!



I am starting to suspect

that I won’t be living long enough

to see England lift the World Cup again…

But I guess that’s not as doomy as it sounds.

 

(The next World Cup will mark 60 years since 1966. If it’s a centennial cycle, for example, I could yet be an exceptionally ancient man and fail to witness the next English triumph)

 




Measured by volume

I am a water addict.

Measured by urges

I am not so sure.

 

It is important to drink two litres per day when on chemo, but the chemo makes it harder to do so

 


    


Never mind why

all this had to happen.

Why did all this have to happen

after I'd retired from paid leave?

 

I had five days off sick in forty years at work. I'm approaching four months in hospital, never mind ill, in the last four years.


Chestnut – tawny – crimson - amber - fawn

Looks a tasteful sequence,

but is last month’s weekly spectrum

of the colours I have pooed.

 

 

Chemo is a chemical blast

that hopes to catch some cancer

in its fall-out.

No wonder I feel rough.

 

 


Four days

of wanting only sleep.

If this were permanent

it might as well be.

 


How come

though I prefer the state of sleep right now,

when I awake

I always hope it's time to get up?

 

It usually isn’t, as I wake every two hours or so



If love’s a consolation

then I have it –

although, of course,

that means there’s more to lose.

  


Now for night

That’s one day fewer

I have left…

Just the same as everybody else.

 


 

This won’t make a TV drama

We know the ‘who’.

We know the ‘how’.

How much can we really scrape from ‘when’?

 

The traditional detective tale is a whodunit. I love ‘Colombo’, which is a ‘howdunit’- or, more strictly, a ‘how-will-he-work-out-they-dunnit’. I’m not sure the ‘whendunit’ is a genre.

 

CYCLE 4



I don’t resent my sleep

the way I used

for wasting time:

I thank its for its service. 


 


The irony is

that now I want sleep I can’t get much:

something in me wakes me

every hour or two.


       

Chemo is set

to sort the problem:

not of dying,

but of wishing to live.

 

       


Diarrhoea or constipation?

The chemo and the tumour are battling it out.

Can’t they reach

a sensible truce?


 


The answer to slow movement

is paper.

For the brain, not the bum,

I ought to add.


I write for Art Monthly as well as reading it.



I seem to have

sufficient people pitying me:

there’s nothing to be gained

by adding myself.


 

This is about as beautiful

as diarrhoea gets.

Don't make me

lift the lid!


 

More of this

and it’s ‘Fuck the Chemo!

Bring on the cancer

and see what that can do!’


Photo is of Hamwic House cancer treatment centre, Southampton Hospital


I’ve had so much

diarrhoea

I’ve almost learned

to spell it!


 

To be regularly irregular

and irregularly regular

have become the ruling rubrics

of my life.

 


 
  

How should I illustrate

What I’ll call the poo-ems?

I don’t like

to use those photographs.

 

CYCLE 5

 


This is my ‘pump shirt’

specially sourced by Steph

with the perfect pocket,

plus style and warmth.

 


Steph is a wonderful organiser

She doesn’t trust me

to be the same -

and she’s probably right.

 

  



How can I not be grateful

to be awarded a Blue Badge?

Well, I see that means my doctor has certified

that I’m likely to die within a year…

 

Online information indicates that my doctor must have submitted an SR1 form to the Department for Work and Pensions stating that I have a progressive disease and, as a consequence, she ‘would not be surprised’ were I to live for less than 12 months. Details redacted.


I need to thank chemo

for my horribly late introduction to male grooming:

face cream is needed to offset

the dry and acned skin effect.


Not that I’ve entered the skin care economy: those creams are Steph’s, the hospital’s, and a specialist recommendation that Gretchen Andrew sent me from California!

 

I ought to look forward

to what could be my last Christmas,

but it’s my fourth potential-last-Christmas

and I think I’ve had enough of those. 


The tree in the cancer centre where chemo is administered 




Boo to you

sore tongue!

I stick you out

defiantly!


Einstein's tongue

 

      

Six months chemo

is likely to last at least seven,

due to breaks, rewarding the bad behaviour

of side effects.


My first 5 x 2 week cycles have taken 13 weeks, due to  week postponements – and that is typical according to medical staff. I wasn't actually in the treatment centre on Christmas Day - the clock isn't set correctly. 


 


Thank you

diarrhoea and mucositis

for my Christmas break,

and a Happy New Year.

 

Mucositis is when your mouth gets sore and inflamed. Like diarrhoea, it's a common side effect of chemotherapy. 




How different is the back of my chemo hand

from how it used to be?

I realise now I can’t have known it

quite as well as I'd have thought…


 Jon Fosse's 'Septology' is my book of the moment

     

Should I mourn 

my loss of pubic hair?

I don’t think so:

people pay to have that done!

 

Fortunately, it being Christmas, there’s no need to get too personal to illustrate bald balls 



I guess my life has shrunk

to the pump and the keyboard.

But give me anti-sickness and a new idea

and it’s not so bad a shrink.


CYCLE 6 


         

2026!

Not one I expected to welcome in:

deserving of a double drink

if that agreed with chemotherapy.

 

That is another view Hamwic House, the cancer treatment centre. 


 

 

I answer to the name ‘His Fluffiness’

on account of my new dressing gown.

If you’re moved to throw in ‘Royal’,

go ahead.

 

  

Give it up for the Friday morning mix…

Double dexa, doxy, codeine, double lop with multivit.

However they land, I guess

they go down much the same.


The more formal description 2 x dexamethasone, 1 x doxycycline, I x codeine sulphate, 2 x  loperamide hydrochloride, I x A-Z complete multivitamin


 


I seem to spend

plenty of time

in pyjamas,

unlikely to fly beyond them for a while.

 

One of my sets is patterned with birds. I’m planning no flights during chemo.


     


My hair is going fast…

Which might be good:

I’ve wondered what I’d look like bald,

but never quite enough to shave it off.

 


The world of logs

covers pills and poos

and appointments and weight

and life moving on towards whatever’s next.



 

I’ve found the key

to chemo comfort:

three pairs of socks

without increasing my number of feet.

 


What if life continues

through some mental equivalent of the Law of Conservation of Matter?

Surely my thoughts will be far too dissipated

to carry on constituting me.



 
 

It’s true I haven’t suffered much

but I have had to eat

crumpets, pancakes and bagels

in an effort to maintain my weight.


I rather like them



At least it means that I can travel

further than I’ve ever done  –

Mars, the Milky Way, planet Twix, the Galaxy - 

by way of chocolate bars.

 


Increasing amounts of loperamide

do nothing to stop me pooing.

I say ‘it isn’t working!’

The doctors say ‘you need more!’

 

The day had a neat symmetry: 8 x loperamide, 8 x poos. My diarrhoea has been the same at 0, 4 and 8 pills daily, but Dr Rees says she has patients on 16 loperamide daily, though the packs say 8 is the maximum dose. Who knows what the dose does?

 

CYCLE 7

 


The steroid night’s

disruptive, but productive:

I’m not sure what to think

of thinking preventing sleep.


 


I believe this is the 5th anniversary

of this kite getting stuck up a tree in the park.

Let that be my metaphor of the day

for cussedly hanging around.

 


Bad news, perhaps?

My skin’s improving,

when rashes tend to correlate

with chemotherapeutic effect.

 


I’ve taken to pooing

in the middle of the night.

Sometimes I make

no sense to myself.

 



Suddenly

a run that's not a run

of seven 4’s on the Bristol scale.

Just a blip, or solid progress?


The Bristol Scale is the medically recommended way to classify stools. 4 is fairly firm, 7 is wholly liquid. 

 

  


Back to number 6

Maybe that sequence

was merely

a flush in the pan.


      

Dry skin alert!

Steph has to rub cream all over me…

I don’t ask her to pretend

she doesn’t enjoy it.  

 

 

 

The good news is

I’m responding to the chemo.

The bad news is

I’m telling it to fuck off.

 

My CEA marker has reduced, but chemo remains an unenjoyable experience


 

Let’s face it

No-one likes

to take pills.

But here we are…


A breakfast mix of 2 x Adcal-D3 calcium carbonate, 2 x Dexame Thasone, I x Doxycycline Capsule, 1 x A-Z complete multivitamin


        

A booklet asks

‘Should I scalp cool?’

It seems like quite a faff

simply to repatronise the barber.

 

I didn’t notice this booklet during my first chemo courses. It proposes wearing a specialised, cold cap on the head. By lowering the scalp's temperature, that narrows blood vessels and restricts blood flow, decreasing the amount of chemo drugs reaching hair follicles - which reduces damage and promotes faster regrowth. The cap is worn for some 30–50 minutes before, during, and up to 4 hours after chemotherapy.




How quickly

norms are set!

If I woke without a sore tongue now,

I’d wonder what was wrong…


CYCLE 8




My tumours have shrunk!

I’ll have long enough to reread Proust

to celebrate finding

the time I thought was lost.

 

A scan revealed that the chemo was working. Among novels, Marcel Proust’s ‘In Search of Lost Time’ (1913-27) is the longest masterpiece - 4,300 pages, over 1.3m words… 

 

 

What's a boon it is

to live five miles from the hospital…

If only we hadn't used to live

just half a mile away.

 


Ha ha, ha ha!

It’s a funny old world

if the best way to take life seriously

is to laugh in the face of death. 


‘We take life seriously, laugh in the face of death’ – Bill Callaghan – 'The Man I’m Supposed to Be', 2026



Apparently I always smile

when the question is asked

and I list the sites of my tumours.

Well, I don’t think scowling will scare them off.

   

What was my hurry?

Almost four years in

I attend a Bowel Cancer Support Group,

discover a community of sorts.

 


The meeting concludes

that it’s easier to reach acceptance

if spared the trauma of uncertainty

by a terminal diagnosis.


 

Most of us will fall in love

all of us in death.

So yes, I am a fool

for death - who isn’t?


Several different songs have been titled ‘Fool for Love’ or ‘A Fool for Love’. I’m most familiar with that sung by Bryan Ferry (written by Ferry and Dave Stewart in 2002)

 

Is seventeen poos in forty hours

enough to trigger hospital admission?

So it seems, to my annoyance –

I have things to do, I have people to see!

 

I was in hospital for two nights


 

Everyone has cancer in ward 4C

but no one else seems well enough

to make the most of that  

as a conversation starter.



I cheer myself up with a chunk of madeira

and an online search for jokes about death:

a dying man’s allowed no cake

because it’s being saved for his funeral…



3 a.m.

It’s time to play my hospital song,

‘I Can Remember This Life’.

Hang on, I want that again!

 

I discovered – and repeatedly played - Julian Cope’s ‘I Remember This Life’, 2008, during my first stay in hospital, in 2022. That's the current - surprisingly subtle - state of my 2022-23 scar.


TWO WEEK BREAK BETWEEN CYCLES 8 AND 9



My ‘chemo breaks’

make plenty of sense.

What's the point of extending life

by rendering it unliveable?

 

From time to time my oncologist postpones a gap in treatment to allow fuller recovery from side-effects.

 


 

What is the cancer doing to me

inside? Is it anything like

what Maggie’s reflective cladding

is doing to me outside?

 

Maggie’s is the cancer support centre at Southampton hospital



 

Bristol poop chart cakes

are an on-line presence:

slightly disturbing,

even if they are made with flour, eggs and cocoa powder.

 


Hello, I am your cumulative effect

Here to tell you not to settle

into an over-predictable cycle.

I don’t expect to be liked.

 

         

How significant can an absence be?

Quite significant, it seems to me,

but only because

I’m present to think so.  


 

I got my Blue Badge

for the likelihood of not lasting a year,

but note that it’s valid for three…

there’s a best-use target!

 



Call it a chemo bonus…

I’ve read almost all

of Volume 5 of Knausgaard’s Struggle

while sitting on the loo.

 

Paradoxically, although I have diarrhoea and the initial movement can be more than urgent, it often takes a long time to issue forth in full. Karl Ove Knausgaard’s ‘Some Rain Must Fall: My Struggle Book 5' comes in at 662 pages. The full cycle of six was first published in Norwegian across 2009-11. Whether I’ll get time to read his second series of novels – as of 2026 he is working on the seventh and final volume – is a moot point. No-one has that much diarrhoea!



Here’s a plan

Die before the ones you love,

before you can be otherwise

affected by death. 


       

Worryingly

I read that, although the sun will not die for 5 billion years,

it will grow too hot for photosynthesis to occur

in a mere 500 million.

 


Home comforts and a wonderful wife

remind me how many

miserable and lonely

endings are available.

 

 

The belief

that I’ll run out of worlds

after this one

makes me a little more reluctant to leave it.

 

CYCLE 9

 


If all I got was chemo-doze

and chemo-daze

I’d knock this on the fuddled head,

but half the time? OK.

 

 

Four years on I haven’t died

Not even once.

Perhaps I will have long enough

to get fed up with life.

                               


Why did I wake with the question

‘Does Burkina Faso still exist?’

Nationalise me now:

the average state lasts 300 years.

 

It’s not in the news much, but that’s its flag, using Pan-African colors in which red symbolises the revolution, green represents agricultural abundance, and the yellow star signifies the guiding light of the revolution. The Republic of Upper Volta gained independence from France in the year of my birth - 1958 – and was renamed in 1984.Burkina Faso means something like ‘Land of the Upright’ in a mix of the two main languages: Burkina is Mooré for ‘upright’ and  ‘Faso’ is Dyula for ‘fatherland’. In ‘The history and future of societal collapse’, 2025, Luke Kemp works with a dataset of some 300 states across the past 5,000 years to conclude that the average lifespan of a state is 326 years, not so bad for a human member – indeed, current life expectancy in Burkina Faso is only 65.

 

 


Given I only just found out

that Albert Einstein said

‘When you stop learning you start dying’

I won’t be starting quite yet.




It didn’t worry me

to come across an apparent end:

I can’t see the real thing

being orange.


 

Maybe Zeno can apply

to death’s arrow…

though I concede

 it hasn’t worked for anybody yet.

 

Applying a Zeno-style paradox would be to suggests that to die, you must first experience half of your remaining life, then half of what remains, and so on, theoretically creating an infinite series of ‘near-death’ moments that can never reach the final and decisive moment. But I guess we live in practice, rather than theory.



I wake, my Panny-thickened

eyelashes all gummied up with scuz.

Is the message not to bother

opening them at all?

 

Thickening of the eyelashes, a little surprisingly in the context of hair loss, is a common side-effect of panitumumab, or Panny, as we and the nurses tend to call it for ease. 


 

Death would be

too much for me today.

Not because I couldn’t cope,

but because I’ve too much else to do.

 

‘Should I have offered to go to the funeral of the girl’s father? Death would be too much for me today.’ – Clarice Lispector: ‘For the Time Being’ in ‘The Via Crucis of the Body’, 1974

 


 

You won’t think

my chemo look is beautiful – 

unless you judge aesthetics

by the underlying purpose.

 

         

Advantages of cancer, Part 3

Dieting made easy, Maggie’s cups of tea,

savings on barbers, nurses good as gold,

all that fucking empathy and not getting old.

 

A take on Ian Dury's 'Reasons to Be Cheerful, part 3', 1979



At what age do you tip

into starting to die?

Whatever, I propose to live

as if I’m not there yet.

 

According to Witold Gombrowicz in his novel Ferdydurke, 1937, as soon as you hit 30, you start dying rather than living – in line with his view that ‘dying’ is the loss of authenticity that begins when society forces ‘mature’ form upon the individual.


 

 


‘Irony’ may be going too far

but, whatever the right word is,

the paper cuts on the end of my fingers

made these lines awkward to type.

 

The medical summary states that ‘Panitumumab can cause some unique skin and nail side effects. You may develop a rash. You may also develop very dry skin, which may crack, itch, or become flaky or scaly… You may develop an inflammation of the skin around the nail bed/cuticle areas of toes or fingers, which is called paronychia…Nails may develop ‘ridges’ in them or fall off. You may also develop cuts or cracks that look like small paper cuts in the skin on your toes, fingers, or knuckles.’ As of March 2026, I have a fairly full score across those minor matters.


CYCLE 10



Why Panny should make

my eyebrows bushier

while the rest of my hair falls out

is baffling enough for a raised response… 


     


Cycle 10 should be like death

You know what’s coming, if not quite when.

Yet chemo is full of surprise effects,

maybe death will be the same.


 

And, so far, Cycle 10 is good

a steady flow of little impact.

What’s gone wrong

to make things turn out right?

 

  


What lies in between 

life and death?

Life, I suppose, 

but hardly any of it.


        

It seems that I am full of shit

and I’m not being insincere,

deceptive, daft, or vulgar…

My stream is literal and plain.



Seven all-too-voluminous times

in seven hours? 

Where does it come from,

especially when my bowel has been reduced?    



My mantra for symptoms is

‘They’re nothing much’. If they were something

I’d have to stop doing things I don’t want to stop,

so they’re nothing much.

 


If life is a funny thing

that happens on the way to the grave,

should I be laughing

or is that for others, after I’ve gone?

 

Quentin Crisp: 'Life was a funny thing that happened to me on the way to the grave' - The Naked Civil Servant, 1968.


      

‘What's wrong with me today?’

‘You're dying’.

Oh yes,

I suppose there is that.




By the time I’ll have finished

acting out my death,

the real thing looks like being

some way overdue.

 

‘In the shadowplay, acting out your own death, knowing no more’ – Joy Division, Shadowplay, 1981.    

 


It’s a shame for Steph

that ‘I will love you till I die’

doesn’t promise

long-term dedication.



For now, at least

I’m too busy to die,

though I guess I’ll get around to it

in the end. 

 

CYCLE 11  



It’s one of those days

when you wonder what it’s easier to survive –

the medicine.

or what it’s up against?



A second visit to the Bowel Cancer Support Group

persuades me that my chemo side effects

aren’t so bad as those of others.

All of whom – oddly – are constipated.


 

It’s curious to be in a social group

whose common denominator

is bowels, tiddly pom,

and the naturalness with which we discuss their movements.


From one poo to another: 'tiddly pom' was one of Pooh's favoured hums in A.A. Milne's books  book Winnie-the-Pooh (1926) and The House at Pooh Corner (1928)



Time vanishes

all the time.

I’m relying on death

to solve that.



What’s the point of an adventure

you don’t actually experience,

however big

the prospect might seem?

 

JM Barrie described death as ‘an awfully big adventure’ in ‘Peter and Wendy’, 1911.

 


Can I write a poem

that doesn't mention

what I'm effectively spelling out now

in the name of its avoidance? 



In our nth appointment with Dr Rees

she says my side effects are worse than average:

she takes my rashes and diarrhoea

more seriously than I do.

 

‘My Medical Record’ on the NHS system shows I have had 120 medical appointments as at April 2026 (many, but not all of them, with my oncologist, Dr Rees)

 


So much so she recommends

I stop the treatment – why object? –

a cycle early

in favour of my quality of life.



I may be a half-full type

yet I acknowledge

that the emptiness exists –

and in time it will be absolute.

  

The long term is as dead

as I will be in it

by which I mean I won’t be in it

to make my meaning clear.

 

 

It’s simple

for mayflies:

They have their dying season

and that’s that.

 

Medical Notes 

My fortnightly chemo regime from October 2025 - April 2026: first Sunday – blood test; Monday – see consultant; Wed-Fri – a combination of 4 different drugs (irinotecan, folinic acid, 5FU, and panitumumab) are given intravenously with a further top up of 5 FU being delivered via the PICC line using a balloon pump for 46 hours following set up; second Saturday onwards – try to recover.

Here's my official diagnosis as at December 2025: 

Diagnosis: · Metastatic colorectal carcinoma (T3 N1 M1c, primary removed, liver, peritoneum). · No DPYD mutation detected. · MMR proficient. · BRAF/KRAS/NRAS wild type. Treatment History: · Oct/22 ascending colonic primary T3 N1. · Nov/22- Jan/23 Capecitabine and Oxaliplatin chemotherapy x4 response to treatment. · Jun/23 exenterative surgery and right hemi hepatectomy. R0. · Decision to proceed with pelvic peritonectomy HIPEC and redo right hemicolectomy. No peritoneal malignancy was identified. · Aug/23 - adjuvant Capecitabine and Oxaliplatin chemotherapy x2 discontinued because of rising CEA. · Oct/23 PET peritoneal recurrence midline and left rectus abdominis muscle. MRI liver no metastatic disease. · Apr/25 PET avidity para-aortic and pre caval lymph nodes and in relation to SMA. · Sep/25 - Multi-site progression - Lungs, single liver lesion, disease encasing SMA. · 10/25 FOLFIRI panitumumab

I reviewed Paul with his wife today. His fourth cycle of FOLFIRI and panitumumab was delayed by 2 weeks because of diarrhoea and then mucositis. His bowels are now opening 3 times a day and continue to be loose but formed. He is currently using 3-4 loperamide a day. His mouth has improved although the tip of his tongue remains sore. He has regained the weight that he has lost. He still has a cracked heel but is moisturising his trunk, feet, and hands. There was no visible panitumumab rash affecting his face, but he does have a grade 1 rash affecting his back. He has grade 1 alopecia. I have advised reducing the FOLFIRI to 70% for cycle four with full dose panitumumab and this is planned for Wednesday. I have also given him some codeine phosphate in addition to the loperamide to experiment as to whether this helps to slow his bowels. I have suggested he starts taking the codeine phosphate at night. We have agreed that he will have a telephone consultation in 2 weeks' time with repeat bloods prior to cycle five. He has a mid-treatment CT scan booked for the 5th of January. The CEA has fallen with treatment.


Photographs

My photos taken at home or at the cancer treatment centre in Southampton Hospital are combined with abstract images - either of things that look abstract up close, or the results of accidental photographs over the years which I have saved for their abstract qualities. Those are supplemented by the occasional playful found image.

 



























About Me

My photo
Southampton, Hampshire, United Kingdom
I was in my leisure time Editor at Large of Art World magazine (which ran 2007-09) and now write freelance for such as Art Monthly, Frieze, Photomonitor, Elephant and Border Crossings. I have curated 20 shows during 2013-17 with more on the way. Going back a bit my main writing background is poetry. My day job is public sector financial management.

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