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What a great start to the day. For starters when I woke up this morning, my eyes were just not interest in getting up, and refused to open. Eventually time and necessity got the better of me, so I got up. Just in time for the postie to deliver something I have been waiting for. My LED spotlights for the light unit in my bedroom.

Unwrapped and installed within seconds...... And they are utter shit! Flash bright then go very dim, which is not use to me. Then to add insult to injury, as I tried to remove one of them, it fell apart. Needless to say I have contacted the seller and am awaiting a reply to see what they wanna do about it. Lesson learned, cheap LED bulbs are NOT worth it!

Then it was dog walking time. Getting it in asap, as mum had a nurse coming late morning. Progress was good, about half a mile from home I got word that the nurse would be home very soon.... So started running. Ran the half mile home only to find that the nurse was already there and in. Tuvaaq was in the kitchen. So that was a waste of energy lol, but a nice run all the same.

Sorry to the people startled by seeing Aana running up the road, I was getting some rather strange looks to say the least. Feels good to push yourself from time to time though I have to say.

Next up, once the carer has been, its off to the pharmacy to pick up a prescription for mum. Another day with lots of walking, seems like they are never ending recently. My intake has gone up a little to allow for this, but not sure where that leaves me weight wise. I am definatly losing more size as clothes are getting looser and looser (and not stretching to match my girth! Lol)

I might have a low intake day in the next day or two and a weigh in to see where I am with weight. Just out of curiosity more than anything. I am happy with my health improvement, that's the main thing. As I said before the next step is toning, and I really must get my finger out and get on with that. Talk is cheap! Time to knuckle down and get on with it. Starting with abs and tri's.

In fact, as soon as I'm back from the walk to the pharmacy, I'm going to do a bit of each, and get this show on the road.

Other than that, life is pretty dull. Thankfully mum has stabilised for the time being. Still a little confused about a few things, but trying harder to eat and drink etc. Still loves to moan and huff about things too.

Just a quick mention to Kim who is in hospital. Hope its not a long stay for you hun, and I will be up asap to see you 🙂 x

Regards
Michael

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Well I'm hoping its just a bump along the way, but not too sure. But mum is now back to not wanting to eat or drink much. Becoming tired and weaker by the day, and relying much more on the wheelchair to get about.

The steroids are being reduced, and since dipping from 2mg twice a day she has slowed down. Even on 2mg once a day she was still eating and quite active. But now on 0.5mg a day she is actually using the walker around the house rather than carrying it, prefers to be IN the wheelchair when out and about, and is really off her food and drink. Its a chore to eat. My worry, dehydration.

Yesterday we went to St Thomas's hospital to get mums "surgical appliance" also known as a wig, which she seemed very happy with. However today while getting ready for St Christophers she said she would not be wearing it as it was a bad fit and looked silly, and quite frankly could not be bothered to put it on.
She added on the that she was "very very sick".

A little while later we toddled off to the hospice for a meeting with Karen the nurse. Enquiring into mums health was like asking a 2 year old where the put the car keys. Not really willing to discuss it much. Changing the subject whenever possible. All the symptoms were to be blamed on any medication that she could remember she was taking, and promises were made that she really has no interesting on following through with. Using a nasal spray, trying to drink more, and seeing the GP later. However she WILL be seeing the GP, I will make sure of that.

A number of things could be contributing to this "bump" in the road but without tests and trying meds we will never find out.

We are returning to the same familiar "no I'm not doing that" attitude, which usually results in an ambulance and a week in hospital. Sadly it seems we have again passed the point of reasoning, and she just thinks doing nothing about it, and sleeping more will solve the problem. So fingers crossed the GP can put her on the right track, although at this rate a referral to the hospital.

So, back from the hospice now, lunch made for mum, just waiting on the carer. This afternoon, dog walks then off to the GP @ 3.30 to get mum seen.

Here we go again?
Regards
Michael

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2

Well its been a very physical day for me today, but let me open with the main point of this entry. My mum, good ol' girl.

I took her to Battersea Park today, I'm slowly upping the scale of the challenge for her, each time choosing a location and route that is manageable but can be cut short. While having interesting surroundings which inspire wholesome conversations.

So today's location, Battersea. A little bigger in circumference than Dulwich I would think, and plenty to look at (a mens hockey game certainly caught her eye lol). Its a lovely park, one full of memories for me, and one of my favourite places in London to relax. So much going on, yet so peaceful too.

When we got there I parked up by the meter, and fed it with the £2 minimum which bought us two hours. After getting mum and the chair out of the car I checked the time on the ticket and said out loud "two hours that should do". Mum replied something to the effect of there was no way we would be that long as she could not walk for that long. Needless to say she was right. She only managed an hour and 49 minutes lol. Bloody well done. Not sure on the distance but a good show! She was very surprised but pleased with herself.

Now to find a bigger challenge for tomorrow lol.

The rest of the day has been pretty ok. Let the carer in this morning, then the daily routine of breakfast (shake) for me, fed the dogs, swept the floors, cleared the garden of doggyness, however I am ashamed to say I forgot mums meds, she actually reminded me today, oops!

When I came back from the morning five miles with the dogs, the carer was waiting on the doorstep, early if you would believe it. Terrified of Aana she stood back while I opened the door, all the time commenting on how cuddly Aana looks.

After finding mum and greeting her they went to the kitchen where they sat and chatted. Mum had some toast and tea for lunch, and they spent the next almost 30 mins chatting and laughing their hearts out. Its refreshing to both see mum and the carer bonding now, and also mum socialising and being so happy and jovial.

Later as we drove to the park she got talking about her hair loss, and commented on the suggestions people made, and how she wants to do her own thing, as its one of the only things she can control. The topic swayed about from talking about what stresses and depresses you, to how you cope with the things that bother you. Another bonding and memorable moment there, where mum has opened up for a bit and let me in.
I mentioned to her during the conversation that it was clear to me that there are still things on her mind that she needs to get out, but that I respect her wishes on how and who she chooses to do that with.

Phew so there you go, digging deep mentally, emotionally and physically all on one day.
Regards
Michael

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Just got back from a lovely walk in the park with mum. All part of her keeping moving plan, giving her some exercise, physio etc. Just got to work out how to get her moving her upper body too and build up some strength there.

She has done really well walking, managing a complete lap of the outer circle and then a lap of the lake too. All at a good pace, without rest. Very impressive if I do say so myself.

Shame it started raining, but we had a good "rush" back to the car. I have to say the conversation was wonderful too. Warms the heart having a chat like that with mum.
Regards
Michael

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Oooooooooooook this is how it goes.

Finally got her to the hospital, parked as close to the dept as possible for her, only to find they have moved it lol. Sister helped her there while I got parked properly and not pay extortionate rates for parking.
Lovely new department, in the new wing, so no more dark broom closet anymore.

Running a bit behind, but got seen within an hour of the original appointment time. Me and my sister waited while she saw the doctor, then when she came out, I popped in. I was welcomed by the doctor and specialist nurse who sat me down and filled me in on the whole matter. Mum had apparently said no to me sitting in previously.
Suprisingly on the journey home she was 100% straight about almost everything said, which was pleasent.

So, the prognosis, outcome, road ahead.
The right side has become very large now, and radiotherapy is not considered a viable option. Chemo "may" have a partial effect, but the preferred treatment is now surgery only. HOWEVER, her COPD is in the way of that, with her breathing being considered borderline too bad for general anaesthetic, so she has to have a complete medical inc scans, xrays etc to see if she is fit enough to even be considered for surgery... not that she has accepted having surgery, but they are thinking ahead.

Unfortunatly, due to the size of the lump now, it would be a more intrusive surgery, with the breast being removed, and her requiring a skin graft to cover it up and help it heal. Given that she was against a simple lump being taken out, I cant see her going for this at all. Myself, the doctor and the nurse are all in agreement that she has made a very rational decision to let the cancer take its course, and to see it to the end with no further treatment. So I am grateful to the doctor for continuing to pursue the surgery route even though its an outside chance.

The COPD is what is causing all her main symptoms at the moment, for which she needs to go back to the GP, so I am in the middle of trying to get that sorted out for her too. Once again, unfortunatly she is unlikely to take on board much of what they say or give her, so the condition will get worse. Amazingly with full blown cancer, its the COPD making life awkward for her now. So hopefully we can get some help for her there, and make life a little better for her, a little mobility and freedom. But the harsh reality is, she is going to need to be watched much closer again now, with the risk of her passing out again.

So the road I forsee is as follows.
Refusal of any other treatments, and letting the cancer take its course.
Supervision from the hospital, and pain meds given to make things comfortable.
Reluctance to get anything done about the COPD
Breathing getting worse and worse.

Hopefully she is "friends" with the doctor again now, and will continue to go there and get help from them, inc pain relief.

Next appointment has been set for within a couple of weeks time, to go to Guys to see the specialist there. Updates to follow.