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

Had a great weekend at home.Had a very painful and difficult night sleeping last night before I had to come back in toda...
28/07/2025

Had a great weekend at home.

Had a very painful and difficult night sleeping last night before I had to come back in today.

The results of my latest MRI scan have confirmed the cancer has spread to my bones and especially my fractured spine.

I've been offered a single round of radiotherapy to try and help with the pain which I am extremely grateful for, just need to look out for the letter in the post as I am currently on my way home! 🥳

I am in terrible pain but I'm home! So happy, yet so emotionally exhausted.

We'll see what tomorrow brings...

Very much love to you all 🥰

xx ❤️🕊️ xx

Day 4...Had my MRI scan this morning. Was in there for a while and think I fell asleep a few times lolGot back to the wa...
25/07/2025

Day 4...

Had my MRI scan this morning. Was in there for a while and think I fell asleep a few times lol

Got back to the ward and got told I could have a weekend pass! I'm over the moon and back home for now.

If the results come back with anything urgent, I've to go back in over the weekend but I'll definitely be back in on Monday.

Crying happy AND sad tears lol. Emotions are all over the place.

Here was this morning's NEW AND IMPROVED breakfast. 😕

Thank you all for your comments, each and every one means so much to me. 🥰

Glad to have my own chairs back! It's amazing all the little things you miss without realising. Even within the space of a few days.

So happy to be home!

xx ❤️🕊️ xx

Day 3...So after waiting for a good while, we finally got my results back from the CT scan.I have a fractured spine caus...
24/07/2025

Day 3...

So after waiting for a good while, we finally got my results back from the CT scan.

I have a fractured spine caused by either the amount of steroids I'm on (which they increased btw lol) or the cancer has spread to my bone.

I've to stay in again to get an MRI scan tomorrow for a more detailed look into things so that everyone has a clearer idea of what's going on, what they can do and how to deal with the next step.

They were nice to let me out to go home for a little bit of time at home which was amazing. Felt like I'd been away for months lol

That's me back in my room again, waiting to see what tomorrow brings.

Big love to you all for following my wee journey. I read your comments every day and they just melt my heart over and over again. I've got the best people on here and couldn't wish for another bunch like all of you. Thank you!

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.

❤️🕊️

Hi! :)Well on Saturday, I had my first cataracts surgery on my right eye. I had been extremely nervous about this proced...
21/07/2025

Hi! :)

Well on Saturday, I had my first cataracts surgery on my right eye. I had been extremely nervous about this procedure as I hate anything near my eyes and the added fear of moving/blinking/coughing etc just that little bit that would tear my eye open lol.

Got to say, every story I heard of everyone who has had it done put me at some kind of ease beforehand and not once did I hear of any bad experiences but you know yourself, it doesn't stop you worrying. So my review?

It was more or less exactly how I thought it would be but only better, if that makes sense? They put a blindfold over my eyes, opened the wee bit so that my right eye could be operated on, put loads of drops in and shone a bright light directly in my eye so I really couldn't see anything.
I could very faintly feel what was going on but I was too busy trying my best to be a statue so I didn't move lol It was bareable and if you are worried about getting it done yourself, I can only add to the loads of people I spoke to about it. Over in 15/20 mins (you wait longer in the waiting room lol)

I've to go back and get my left eye done at some point but I know now what to expect and I will go happily to my next appointment with so much less nervousness and worries. Thank you NHS! Another job well done!

Thank you all for your kind words of support and for the many donations towards my 'Celebration of Life' night, I am overwhelmed by so much love from you all! THANK YOU!!! xx ❤️🕊️ xx

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