Dove & Sarah's Final Quest

Dove & Sarah's Final Quest My final quest for raising money for myself and my family, to enjoy life before cancer wins the fight

24/08/2025

Just to keep you all updated with everything that's going on at this end. The stuff you don't see or hear about that we have to deal with behind the veil of what you see when we're out and about.

Every night I try to go to sleep in bed, or a chair, or a special reiki chair that I can lay upwards facing down.

I am VERY limited to which way I can lay and it often becomes a major problem just adjusting for the night to begin with.

I am in a much more constant pain from along the bottom of my stomach/rib cage all the way across from one end to the other, leaving me literally gasping for air to try and breathe, even just a little.

I feel that my breathing has dramatically been less than quartered and it takes me quite a while to resolve getting back into normal breathing again.

It's really very scary having to fight for a single breath and calm down to have some kind of oxygen intake.

The pain in the whole of my torso doesn't help at all and I feel like I'm just going to collapse in a heap of painful noises, struggling to call for help.

I can't sit up myself which means I have to wake Sarah each time I need to move or I'm in a great deal of pain, stuck, until I can move.

Throughout the night is the same, even with all of my medication and more! Night time is the worst. I can either have a good sleep that involves everything I've just written, or a bad sleep where I've been laying the wrong way, even just for 5 minutes and it will mess me up for the whole next day and I'm in pain for the next few hours after I get up.

I usually have to get up between 6am - 8am because I just can't get back to sleep because of the pain.

Once I'm up, I cry at what life has given me. I can't believe this is what my life has become.

I sit and contemplate what I can do to make things easier for everyone but I just can't. My mind and my body just don't work the same now. My most common phrase now is 'OWWW' and believe me, it's said constantly every time I move in sharp intakes of breath.

Sarah needs to help me get up from a seated position, I can't reach anything behind me or even to the sides, just a few inches away from me.
I can't move anything around me, I can't pick anything up or go down to get it, so once it's on the floor, it's on the floor.

My back is in terrible agony at all points throughout the day. Even walking to the toilet/getting up from the toilet is a mission.

The most trivial things are out of my reach now like filling up a bottle of water that's too heavy for me, carrying a plate, getting my slippers on, opening a bottle of juice, passing something over that's laying right next to me, etc.
I feel like I'm just a blob waiting to be served by my queen. I can't do a fu***ng thing and it's frustrating the hell out of me.

People say 'Oh You're the strongest/bravest/most positive person I know', well, it's getting really hard to try and be that person when your world is literally falling apart right infront of you.

Every day I look in the mirror, all I see is this old, dying vision of me that just won't give up but I can see my body trying it's best to shut down bit by bit. It's like I'm decomposing in front of my eyes, just waiting for death to come and take me. I can feel it surrounding me and there's nothing I can do to stop it.

I would really like to make videos to show you all just how bad this is but I'm no good on camera and wouldn't know what to say. I'm not a Tik Tok kind of guy.

In other news, the palate my mouth has basically completely gone, leaving it so damn difficult to eat and drink without choking on air and my speech is all over the place. I'm surprised some of you can understand me now.

Little jobs around the house are completely out of my reach now, dishes, cooking, taking rubbish out, cleaning rooms, moving anything, I can't even pat the cats ffs, so this has all fallen for Sarah to do and that frustrates me even more just watching Sarah struggle to do stuff that we used to do together.

I can't even put a sentence together without getting out of breath and breaking it up into 4/5 parts of breath.

We don't have a couch we can sit on together! In our living room, we have 5 different chairs so that I have different seating options.

I'm constantly asking Sarah if she could do this and do that for me like a bloody servant girl. She is amazing and is ALWAYS there for me at every request no matter how small.

Anyways, my feet have swollen up for a good few months, that's why you might see me in massive slippers I had to get from Amazon because none of my footwear fits anymore. I'm on water tablets for that so YAY! More tablets! On top of more steroids and more painkillers!

We destroy ourselves nearly every day knowing what life has in store for us and seeing it go downhill very quickly.
We know what is going to happen but it's the darkness of not knowing when. Trying to make the most of each day is becoming harder and taking more and more out of us.

Still waiting to see (excuse the pun lol) if I'm going to get my other eye done with the cataracts. No word yet.

I'm very old, feeble and fragile now. Nothing like how I was even just 2 months ago. It's funny how life can change in the twinkling of an eye.

Life really is precious. Hold on to it for as long as you can because one day, you'll not be able to do the same stuff as you can right now and it will change you forever. Stay young!

Very much love to you all for still staying with us on our journey.

Dove & Sarah
xx ❤️🕊️ xx

02/08/2025

On Thursday, me and Sarah went to the radiotherapy bit at the Beatson.

It turned out, it was just to get a CT scan to discuss Friday's single round of radiotherapy and mark me up so that they know where to fire it at me.

We were told that the cancer in the lining of my lung on the left side has got bigger and is pushing it's way even more into my lung and nerves.

The point of the radiotherapy is to try and slow it down and to ease the pain, even just a little.
I'm at the stage where I'll try anything for the pain.

After my radiotherapy session, I am still in loads and loads of pain despite taking everything I possibly could. I know it doesn't magically work in seconds but I do feel a small difference with potential.

We'll see what happens over the weekend and keep our fingers crossed that this helps, even just a little.
I would be very much grateful for some kind of release, just for a few minutes would be nice.

Every morning now, my breathing is severely hard to deal with and it doesn't feel like I can get it back under control for a good while. It is really scary and puts me into a panic.

Somehow I get through it, only to feel like I'm in my 80s/90s throughout the rest of the day.

I need help up from wherever I'm sitting, I can't do a damn thing and it's really getting to me in so many different ways.

I feel like giving up, but with you all here, with your support, love and kindness, I know I will battle on...

Much love ~ Dove & Sarah.

xx ❤️🕊️ xx

So yesterday, we attended my usual check up appointment at The Beatson Clinical Research Unit with the Professor.After a...
23/07/2025

So yesterday, we attended my usual check up appointment at The Beatson Clinical Research Unit with the Professor.
After a wee listen to my lungs, he suggested that I go for a CT scan as it didn't sound right and the pain has just been getting out of control.

I managed to get an x-ray and was maybe thinking I could go home afterwards. I was in overnight. The x-ray came back and they found a grey area around the bottom of my left lung.

At this point, they don't know what it is, could be a collapsed lung at the bottom of my left lung, muscle pain, the cancer spreading, fluid, etc, I even got tested for covid.

So here I sit, awaiting a CT scan for us all to find out more.

❤️🕊️

24/06/2025

The Rabbit Hole

Today I have a new pain, one I've never had before,
It seems to happen every day, leaving me feeling sore,
I know it's probably nothing, that it's all just in my mind,
I don't want to overthink it but it really hurts inside,

My mind, it starts to wander, down the rabbit hole we go,
Is it this?, is it that?, I'm never going to know,
My paranoia sets in, I start to think the worst,
Maybe one of my cancer sites has finally just burst,

Do I sit here in a panic, and see if it goes away?,
Could this really be my final time, on my last day?,
The further down the rabbit hole, the more I overthink,
I sit in tears just crying, as my mind begins to sink,

I start stupidly imagining, if it's time to say goodbye,
That I never had enough time to hug once more, just once before I die,
All the things I planned to do are gone, just left incomplete,
If only I had tried a little harder, this disease I might have beat,

The pain starts dulling down, maybe I was daft for thinking that,
But then it starts back up again, was it the way I sat?,
Is this new pain going to stay with me, an addition to the rest,
Will it go away again, or match the others in my chest,

Every little pain, sends my head into a spin,
Knowing that I'm fighting a battle, I'll never win,
Leaving family behind to deal with this seems very unfair indeed,
They've already been through so much and this they didn't need,

Each morning I go through this, with tears upon my face,
With each new pain emerging, each in a different place,
I know one day it'll happen, I just worry when and where,
Could it be today? could it be next week?, it's just not fu***ng fair,

Watching my family go through this, has been the worst thing from day one,
I've tried to create memories, to give them something to look back on,
I wish I was there for them, on the day my light goes out,
To tell them that I loved them, I was happy, smiling without doubt,

I didn't have the greatest life but with them I had the best,
I'd love for them to know that, because I've deleted all the rest,
This rabbit hole is sinking and I'm looking for a sign,
To bring me out of my misery, each and every time,

I go through these thoughts of what ifs, before the day awakes,
And all the little stupid things, that this rabbit hole just makes,
I know I'm not the only one, Sarah gets stuck here too,
We both sit in this rabbit hole and there's nothing we can do,

Please don't forget that she has been through this just as long as me,
So please don't dismiss her even though she's cancer free,
I always feel that people focus on the cancer man, pushing her aside,
But she has done an incredible job you'll never see, and with so much pride,

So please don't ignore her work, she's done her very best,
At providing me with everything I need, even helping me get dressed,
Please look after Sarah and my family, when I'm no longer here,
Because the fact that I can't do it now, is my only fear,

As I think back, to the pain that put me here, down this trail of thoughts,
In this bloody rabbit hole that we seem to visit lots,
I think maybe not this time, maybe not today,
The pain might dull down or maybe it will stay,

But either way I know, that my family is there,
To help me through the newest pains that give me a little scare,
I wonder why I'm still crying, just a silly old man,
Limited to what I can do, but still doing what I can,

I'm ok I think, I'm sure I'll make it through the rain,
Until tomorrow morning comes and go through it all again,
With Sarah by my side, we can see a beaming light,
We hold on to each other through the darkness of night,

Being down here is nasty and has really taken it's toll,
But I think I finally found a way out of this rabbit hole.

https://gofund.me/dac5dd4c

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