CHEMO RECHALLENGE DAYS 193, 194 & 195

Fight, and know your strategy.

Friday and in a determined effort to be ready for the visit of my youngest daughter and her family, including the two youngest grandsons my partner and I go to the garden centre for breakfast. In an attempt to fuel myself for the day I order the largest English breakfast they have. A rare treat, which I enjoy heartily. Once full of breakfast my partner and I go to the food hall and lay in provisions for the weekend family visit. Returning home we squirrel away the food and with a delivery from Tesco due later in the day I am beginning to think that we could do with a larger fridge/freeze.

I spend some watching the tennis and being impressed by the fact that a British player actually won and progressed to the quarter finals, in fact two British women reached the quarter finals. The day progressed to yet another world cup football match involving one of the hosts Canada. It was a scrappy game with the hosts grabbing a draw late on. In the middle of the game Tesco deliver early and mid match we are faced with getting all the food stashed away. I eventually went to bed having taken my meds and focussed on getting up early to greet the visiting family.

Saturday and the news is that my youngest daughters family are ill, a tummy bug has laid them low so they are not coming today, maybe tomorrow. I am disappointed but pleased they are taking the sensible decision. I take to watching the tennis again and remain impressed as the British number one wins and gets a place in the semi final. My partner and I return to our favourite garden centre to buy “million bells”, a small plant that flowers profusely and does well in our garden. Of course while there we pop into the café and indulge in a bacon roll and a decaf coffee, which I have found my body will tolerate. Once home my partner head to the garden and finds homes for all the new plants. I do potter for a bit in the garden but I am not much help and end up watching the British tennis player play for the second time in the day and winning a place in tomorrows final.

The evening slides into world cup football I confess that I am suspecting that I am already beginning to get tired of it, even at this early stage. The patterns of play are all very similar and the creativity on display is low. Occasionally someone scores a really good individual goal or there is sufficient needle in the game to provide level of entertaining brutality. I watch the late game, take my meds and go to bed in anticipation of tomorrows visitors.

Sunday and I wake up to the news that Scotland have won there over night game at the world cup, which has pleased a friend of mine who stayed up in the small hours of the morning to watch the game. The next message was less happy, my youngest daughters family continue to be ill so will not be coming to visit at all this weekend. I am disappointed but it is for the best, you cannot be traveling around ill with two small children. There is a mountain of food to reorganise so there will be some freezer activity and reorganisation of the “stores” to be done. I get up and have breakfast and fill in my world cup wall chart with the overnight results. then catch up on drafting the blog.

When I come to take my morning meds I realise that I have run out of the twice daily steroid that I take. Because I delayed Cycle 8 by a week it means I am five days short of the daily steroid. I am not bothered really, five days without them is not going to do me any harm and if I am deemed unfit for Cycle 9 or I decide to discontinue to stop the chemo rechallenge I will be stopping them anyway from Wednesday when my next oncology review takes place. It neatly brings me back to the decision I have to make about continuing with the Chemo rechallenge. At the moment I do not know as I have pinned my logic on the out come of tomorrows blood results. If the PSA level is reduced (by how much is another question that I need to think about) then I have to seriously consider continuing as it means the chemo is actively working and it seems illogical to me to stop a treatment that is demonstrably affective. Driving the PSA level to as low as I can get it seems to me be the aim of this treatment. If the PSA level has decreased by a significant amount in tomorrows bloods then Cycle 9 looks like the reasonable choice. What is a significant amount? To be honest I do not know, but I do know that when I see the results I will either get a feeling of “that’s good or not bad” or an instant heart drop moment of disappointment. If it is the latter then its probably time to stop. The drop in the PSA will have to have been worth the post chemo crap that I went through on this cycle, some of which I am still experiencing. It is a fine balance but I am craving a period of rest and a chance for me to recover some of my energy and a chance to build up some strength.

So for today I prepare for tomorrows bloods by drinking lots of water, to boost my platelet reading, and to potter in the garden till my energy runs out and I retreat to tennis and football on TV. Tomorrow is a crucial day, it is also the day the BT engineer turns up to put us on the fibre network. I have no idea how that works, I am hoping it is a straight forward process where he plugs things in and then buggers off and the world continues as before, given that my current broadband works perfectly well. In the meantime I will see if Radacanu can win a tennis tournament and whether Germany can beat Curacao football minnows.

While watching the British tennis player loose the championship final my new poetry collection is delivered. It is Idanre and other Poems by Wolfe Soyinka, which I discovered, or at least the poet, while watching a programme about Mahomed Ali. Wolfe Soyinka read a poem about Ali at the end of the programme. I only found out that he is a Nobel Prize winner for literature in 1986 when the book arrives. I try to read some of the poems and realise that these poems are going to need some time devoted to them.

My latest collection of new poetry from a new poet to me.

I spend the evening watching football and checking my emails. I find that there is a draft edit of my next poem collection from the person who is editing them for me. So over the next few days I will be going over the edit to see how much needs changing. For now its time for bed.

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My life clock still repels the winds of change and time.
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Still want my time with you
Yep, life is full of surprises, like pixies

CHEMO RECHALLENGE DAYS 191 & 192

Fight and never regret it

Wednesday and a day of torrential rain but also the day that my partners mother moved to her new care home, so at last she is somewhere safe and caring and not in a hospital. I of course got up late and spent most of my day finishing reading (what a luxury) Before I knew I Loved You, the sixth book in the Before The Coffee Gets Cold, by Toshikazu Kawaguchi. It is a lovely book and he keeps finding ways for people to travel forwards or backwards in time without changing the present. It is typically Japanese in sensitivity and delicate handling of emotions.

My reading for the day. I recommend it.

By mid afternoon I had finished the book and turned to the Queens Club tennis tournament for entertainment. So I watched two players slugged it out until rain stopped play, by which time my partner has returned home from seeing her mother into her new care home.

In the evening my partner wen tout with a friend for a meal and left me to do a Tesco order and to watch the last friendly football game England were due to play before the World Cup starts properly tomorrow. The kick off was delayed by an hour till 10 o’clock due due to the huge thunder storms in Florida, after which England won 3-0 against Costa Rica. It was midnight before the last kick of the game by which time I was ready to down my meds and get off to bed.

Thursday and I wake up knowing that today the world cup starts and my giant wall chart will need to be got out and activated. My partner goes off to the physio after bringing me a hot a hot water. I check my messages and news feeds before tasking my vitals. They are average, which is okay for me. When I finally get up I head for the shower, noting on the way that the heating had come on, so not only is it throwing it down with rain but the temperature had dropped markedly as well. I do not expect the heating to come on in June! Feeling clean and refreshed I cook myself a cheese omelette and tomatoes, take my meds and start on some life admin. Fiddly little jobs like checking the stray lotto ticket and paying the window cleaner by BACS. They all take time and are all inconsequential, unless of course the lotto ticket is a winner and the window cleaner is not suing you for non payment. Its amazing how “little things” can become monstrous for the lack of attention. Once again it teems with rain meaning that the tennis is delayed, so I start to draft the blog for yesterday and today. There is a final Tesco order to be done and organising for the visit of my youngest daughter and her family at the weekend. It seems that there is quite a lot to do before I get to watch the first world cup football match this evening and begin to use my giant world cup wall chart.

In reflective mood I was thinking about the course of my cancer experience and had the sense that this has been going on for a while with all its changes of medication and fallow times so I returned to looking at all the phases the blog has been through that reflect this process. There have been some prolonged periods of relatively good wellness and other periods where what was to happen next was in the balance. This current period of rechallenge is 192 days long, during which my PSA has been going down, so a reasonable period of success against the disease, but in which I have suffered more physically than since my original chemotherapy. So it seems I have to calculate the balance between how I am physically and what gain there is to be had from further chemo rechallenge. The PSA level as measured by Mondays blood tests will give me some idea.


BLOG PHASES AND DURATION IN DAYS

WELCOME ALL: 01 SEP 201 TO 01 SEP 2019 1 DAY
INDUCTION DAY: 02 SEP 2019 TO 02 SEP 2019 1 DAY
CHEMO DAY: 04 SEPT 2019 TO 05 JAN 2020 120 DAYS
FINGERS CROSSED PHASE: 07 JAN 2020 TO 23 MAR 2020 77 DAYS
AS GOOD AS IT GETS PHASE 1: 24 MAR 2020 TO 08 FEB 2021 322 DAYS
AS GOOD AS IT GETS PHASE 2: 10 FEB 2020 TO 21 DEC 2021 315 DAYS
ANTIANDROGEN: 22 DEC 2021 TO. 22 FEB 2022 63 DAYS
AS GOOD AS IT GET AGAIN: 23 FEB 2022 TO 31 OCT 2022 251 DAYS
ROCKET: 01 NOV 2022 TO 21 DEC 2022 51 DAYS
ROCKET BOOSTER: 22 DEC 2022 TO 06 MAR 2023 42 DAYS
RUN UP TO RADIO THERAPY: 07 MAR 2023 TO 17 MAY 2023 72 DAYS
NO MANS LAND: 18 MAY 2023 TO 29 MAY 2023 12 DAYS
REARMAMENT: 30 MAY 2023 TO 07 JUNE 2023 12 DAYS
REARMED: 08 JUN 2023 TO 09 JUN 2023 2 DAYS
CHEMO II: 10 JUN 2023 TO 18 AUG 2024 435 DAYS
ANGINA ADVENTURE: 19 AUG 2024 TO 25 SEP 2024 38 DAYS
CHEMO II THE RETURN: 26 SEP 2024 TO 13 APRIL 2025 199 DAYS
MOVING ON: 14 APRIL 2025 TO 16 SEPT 2025 155 DAYS
WITH A DASH OF STEROIDS: 17TH SEPT 2025 TO 12 NOV 2025 57 DAYS
STICKY WICKET: 13TH NOV 2025 TO 01 DEC2025 19 DAYS
CHEMO RECHALLENGE: 02 DEC 2025 TO today (11-06-2026) 192 DAYS


TOTAL BLOG DAYS TO DATE:11th June 2026 2476 (6 years 9 months 11 days)

I guess it will depend on how I view the balance and what I consider my priority, quality of life or longevity. Somewhere in there I am hoping for a sweet spot.

.

The evening arrives and I settle down after tea and watch the long drawn out opening ceremonies of the World cup. It takes hours to get to the actual first game, Mexico v South Africa. With football over for the day I take my meds and head for bed. Tomorrow is a chore day in readiness for the visit of my youngest daughter and her family

.

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So this is June is it!

CHEMO RECHALLENGE DAY 190

Fight and grit it out.

Tuesday and I wake up not quite as chipper as I was yesterday. I drink the hot water my partner brings me before she goes to the gym to do aqua aerobics. I read my messages and news feeds before taking my vitals. My blood pressure is still good and my heart rate is maintaining its lower rate. Eventually I get up and have pizza for a late breakfast along with my meds. I do the days crosswords and watch the women’s tennis from Queens. Over the course of the morning and afternoon I get to see two English women get through their first round matches. My partner returns for lunch and is then soon away to see her mother into the new care home. I continue to watch tennis and do odd cleaning chores. I find an interesting array of objects and bric-a-brac down the back of, and under the reclining sofa in the lounge. Amongst the debris was the pen top I had mislaid yesterday, so I am content with the outcome.

The garden guy arrives with a pick axe and sets about cutting back the bamboo that the neighbour had noted was up against their fence. The work goes well and in the end the bamboo is separated from the fence by a solid plastic membrane, which holds a pebble pit. There is no way the bamboo will clump that far again for at least seven or ten years, so it will not be any concern of mine. The garden guy then sets about weeding out the flower beds until he finally waved good bye.

All this time my partner and her brother were waiting for their mother to arrive at the new care home from the hospital recovery unit. At almost 5 o’clock there is still no sign of their mother being delivered to the care home. It appears that early evening is going to be the soonest. I continue to draft the blog and think about food for the evening and suspect that this might be a take away day. My evening will drift into the England women’s football qualifier against Ukraine tonight at 8 o’clock. While I wait to see how the evening is going to work out I get another version of the cover for my next poetry collection. The person doing the designing has done a really good job. There is a small tweak to make but I think the design is very clean and direct. I am happy with what will be the finished version.

It turns out that my partners mother does not get moved and the whole thing is delayed until tomorrow. So the evening slides by with two football matches and the final draft of the blog before I take my meds and go to bed hoping for continued recovery.

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Maximize the inner sloth.

CHEMO RECHALLENGE DAY 189

Fight and brawl rough.

Monday and I am awake quite early so I have time to view my news feeds and messages and then take my vitals. My vitals appears to be good, the blood pressure is continuing to be regular however my heart rate seems to have settled a bit. This seems to coincide with my feeling a bit better and less fatigued. I get up and cook a substantial breakfast that I take my meds with. I settle down to start the draft of the blog until my partner returns from the gym. I poem that seems to echo my up turn comes to mind.

537
There is a sunrise
In my heart
as suddenly my fatigue
takes flight.
Unknown forces are at work
in mind and body
as I glimpse
my old self reappearing.
My heart rate slows,
my breathlessness eases
and for the first time in weeks
I dare to think of training
and of trips out.
It is the tip toeing of
the quality of life
that sees me smile inside
and sensing a happy heart.
This sunrise warms me
as I trust that this is not
a false dawn.
I’m on the up,
and in the distance
the death knell of chemotherapy
tolls out.
There has to be a life
for it to be worthwhile
to fight to live,
and now I know
what the balance is.

537 08-06-2026

My afternoon continues with reading as I try to catch up with my reading pile and to once again feed my brain. I feel like a chrysalis about to transform but have no idea what creature I will emerge as. Hopefully something colourful.

The evening goes by in a combination of tennis and an American police drama. I take my meds and go off to bed hoping my perceived improvement continues tomorrow.

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A sunrise everyday.

CHEMO RECHALLENGE DAYS 187 & 188

Fight without fear

Saturday and I wake feeling not so good, so I rest and take my time getting up. I brief breakfast and morning meds before I settle down to a day of sport. There is football, rugby, grand slam tennis and Australian Rules football. I sit and watch it all feeling fatigued and having little or no energy. My family get on with life around me until they go to the theatre in the evening leaving me to order an Indian take away to eat while watching England field two separate teams against New Zealand. It was an unedifying watch and was really no more than watching two teams jog about in the Florida heat. At the end of the day I watch Blade Runner 2049 and go to bed late.

Sunday and I wake up knowing I had a curry the night before, so I take my time getting up having taken my vitals. My blood pressure remains good but the old heart rate is still elevated. By the time I am up my partner is in the garden putting in the new plants she bought yesterday. I eat breakfast and then head for the garden, by which time the garden guy has arrived and is getting ready to mow the grass. My partner redirects the garden guy and soon we are all planting things. I rescue some large pots and plant up the impulse buy dahlias that have been sitting around for a couple of weeks. I also add additional support to my growing purple sunflowers and finally get round to planting the Rudbeckia seed card that a friend sent me. The garden guy empties some pots for me and transplants their contents into a spare area of the garden. So for the next few hours there is three of us working the garden until there is quite a transformation, everything is so much tidier and we have the next phase of flowering in place.

The garden has some spectacular elements to it. Some of the special stuff is purely by accident where plants have been moved to see if they will survive while others have self sown. I take the camera into the garden to see if I can capture some of the sights.

By early afternoon everyone is tired and we pack up the garden tools and tidy away the pots and plants. A final watering to make sure the new plants are settled in and we are finished for the day. My partner and I eat lunch and start to watch the Paris open men’s tennis final during which I start to draft the last couple of days blog. After a combination of tennis and athletics the family the evening meal and I settle down to watch Shades of Blue before finally taking my night meds and going to bed feeling more hopeful for tomorrow given my gardening activity today.

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Nothing clashes in nature.

CHEMO RECHALENGE DAY 186

Fight and then go again.

Friday and I wake up late. I am surprised that its gone 10am. I did not expect to sleep this deeply. I quickly check my messages and newsfeeds and then measure my vitals. My blood pressure is good but my heart rate is still elevated. Out of interest I weigh myself and find I have lost weight, about a kilo and a half. I put it down to no sweets and Lucozade for a while. I finally get up and make myself breakfast. It seems I have fallen into a habit of cheese omelettes and peeled tomatoes, which seems to sustain me well till the evening meal. With a late breakfast done I sort out the outstanding window cleaner debt and then settle down to watch the men’s semi finals at the Paris open tennis. Its not hugely inspiring so I draft the blog as I wait for the Tesco order to arrive.

Today is yet another rest day. It feels like I am not recovering as I thought I might on a reduced chemo dosage. It is disappointing but I have no other option but to keep going. I cannot see my going for another cycle unless there is a a big decrease in my PSA as a result of the current cycle. It seems to me that my next move is to get some Quality of Life for as long as possible.

Today the England women’s football team play Spain in a world cup qualifier, so my evening is taken care of. In the meantime I continue to wait for Tesco and for the garden guy to turn up and begin to tidy up the garden, probably by mowing the lawns and doing some weeding. So there will be a burst of activity and then I shall retreat back to my resting.

Well Tesco turned up but the garden guy did not. As for the England football team, they got their arses handed to them with a four nil defeat. I close the evening with my meds and a relatively early night.

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Quality of Life?

CHEMO RECHALLENGE DAY 185

Fight, Fight, Fight.

Thursday. I wake tired, my partner and eldest daughter already out of the house. I go through my morning rituals and take my vitals. I try to take stock of how I am, my conclusion is that I am not in the best condition. I scribble a poem that reflects this assessment.



536
There is nothing to say
beyond the desert
of defeat.
Crushed by chemo,
ground by toxicity
I lay alone, desperate,
for in this instant
I can see no glimmer
of me in the future
with energy.
Quality of life
is not in my grasp
but an idea waved
at me by caring medics.
I am suspended,
a strange fruit
neither fallen
nor ripened,
waiting to be
harvested.

536 04-06-2026

I check my vitals, they are okay but my heart rate persists a little high. I take a shower while I feel I have the energy to do so and then make a late breakfast. With food inside me I settle down on the sofa and start to draft an email in response to a poetry stanza discussion. I eventually get a draft done and sent. My partner returns home and is happy that some of the issues related to her mother have been sorted as a preferred care home is going to take her early next week.

The afternoon is full of women’s semi final tennis as I rest and see if the paracetamol helps. The paracetamol sees me through the Paris semi finals and into the evening. The family eat tea together and I then order a Tesco delivery for tomorrow. With that done I spend time down loading a new channel onto the TV so that I can watch the new Brokenwood Mystery series. I check the poetry stanza discussion that is going on and note that it seems a poetry celebration at Christmas looks like a popular option. At the end of the evening I take my meds and head for bed.

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cast in iron I will survive.

CHEMO RECHALLENGE DAY 184

Fight and stay at it.

Wednesday and its been a crap day. I managed to mend and refit a toilet seat, which induced an hour and a half nap. For the rest of the day I did nothing but rest as any activity just brought me to a stand still, or more accurately a sit still. So at the end of the day its meds and bed for me. I’m getting fed up with this Cycle of chemo.

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staying centered

CHEMO RECHALLENGE DAY 183

Fight and stay focussed ahead.

Tuesday and after a reasonable nights sleep I surface and do my early morning checks. I am instantly aware that I am fatigued as I check my messages and news feeds. I check my vitals, which remain stable despite the slightly elevated heart rate. My partner goes to the gym to do aqua aerobics and I make breakfast. As I am late up I go for pizza for breakfast. Having eaten I set about filing my drugs dosettes. It takes more time than usual as the neuropathy in my fingers slows the opening of the pill packets, however I get it done. Because I have delayed the current cycle I am short of one of the steroids I take. I will have about five days short, which I shall either tolerate or get some more if I can face the faff of doig so.

Very little happens after this activity as all I feel able to do is rest and listen to episodes of Just a Minute. The postman delivers my oncology letters, which I file before my partner returns for lunch. It is not long before she is off to see her mother in hospital with her brother. She has a busy schedule as she and her brother are also going to look at another care home. From there she is picking up a friend to go for a meal this evening. On checking my emails I found one from a poetry competition that I had entered. Of course I had not one, in fact I did not even make the “long list”. It is abundantly clear that my poetry is not acceptable and is not in any way aligned with the poetry mainstream or in fact any stream of poetry. Clearly giving poems numbers and regarding tittles as a sign of failure severely hampers my poems ever being competitive. Perhaps the bottom line is that my poetry is just crap, which is not inconceivable. I note that another poetry magazine is open for submissions so I might try and write something for it outside my current series for The Rechallenge collection.

I nibble my way through the afternoon and type odd notes and ideas but nothing coalesces. I am not sure I am functioning well enough to generate anything of interest. I continue to jot stuff and then turn to the blog to daft. A friend rings me as she is out and about doing chores before returning home to do the family tea. I enjoy chatting about our families and what we are currently doing. My evening looms into view. I shall be watching a football match this evening and once again heading for my evening meds and the hope of a good nights sleep.

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A view to reflect upon

CHEMO RECHALLENGE DAY 182

Fight and be tenacious.

Monday the first day of June and I wake up feeling decidedly shaky. I check my messages, emails and news feeds before I take my vitals. My vitals are more or less okay but my heart rate is still elevated. Having listened to Ten to the Top I finally get up and get breakfast hoping to be able to get into the garden but it becomes very obvious that I do not have the energy to do so. I eat breakfast and then spend time ruling up my daily journal. I listen to several radio comedy shows and try to relax. My partner finally returned from the gym. The next door neighbour calls in and tells us that the people we use to do our hedges is coming to do them on the first of July. It is an arrangement that we have our neighbours so that the hedges of the gardens get done together and means the team can work in both gardens at the same time. Its an arrangement that seems to work well over the summer.

I spend quite a lot of time thinking about what sort of cover design I want for the next poetry collection. I research some images and eventually decide that I like the idea of a café with a neon sign that says PSA. The obvious image that comes to mind is Hopwood’s Nighthawks. An amazing painting but captures the kind of surreal feel I like.

This is the look I’m hoping for with some cancer related additions.

At lunchtime I go for the luxury of melon and ham in the hope that I will be able to taste something, however what I experienced was the chill of the melon. I start to draft the blog while listening to more radio shows. Of course the Paris open tennis is available alongside reading and writing, so my afternoon passes interrupted by the occasional unintentional nap. I poem sums up my day so far.




535
Shaky
not a good way to start the day.
My head is at odds
with my body,
so much to do
and so little resource
to be doing it with.
Its rest or collapse,
submit or crash.
So this is me being
over optimistic,
feeling bad that
I cannot contribute
beyond survival
tasks.
So I sit
and wait
feeling
guilt.

535 01-06-2026


By the evening I eat tea and watch almost all the last episodes of Bay of Fires before taking my meds, finishing the blog and finally going to bed. I am hoping that tomorrow I begin to feel some relief from the chemo fatigue and at least a little less shaky.

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Over and over again there is a tomorrow.