Well hello my lovely people.
I’ve been trying to reply on the site, but as we all know it’s not working very well right now.
I’m so touched by all the messages you have been sending to me and I’m so sorry I haven’t replied individually. I re-read everything this morning at least twice and it’s been wonderful.
I think people have asked me for an update, so I’m going to do one.
I’m in Saint Christophers Hospice in London now. I was admitted for pain management and I have to say they have done a magnificent job. I’m not going to be going home from here. This is going to be where I end my life.
I’ve had a couple of interesting conversations with the nurses and the doctors. They can never give you a clear picture of your prognosis, we all know that. But my sense is that I’m becoming sicker each week and that I can expect to have a few weeks left now. I am free from pain. I’m free from any distressing symptoms. I’m in a kind of bubble where my physical needs are being met and also my mental and spiritual needs. You guys are really helping with that.
All the right decisions have been made regarding the future of my daughters. There is nothing outstanding. All I need to do now is let go. I have been fighting for so long that I find it incredibly hard.
The one outstanding thing is my funeral. I am planning that at the moment I will be having a small family cremation. Then later when there is covid lock down his open my family will organise a massive party in a field in Devon. So there won’t be any live streaming, sorry, just not me. But I’ll try to find a way to let you know when it is so that you can think of me. Maybe it’s an anomaly. I’ve been so public about everything I’ve experienced and gone through and now when it comes to a public event, I want to be private. I don’t know. It’s just how I feel and that’s what matters now. Also I don’t think my family would like it, and they really matter.
I’m going to carry on posting. This is not goodbye. Well it kind of is an opportunity to say goodbye just in case. But hopefully not. My love to each and everyone of you,
Daloni XXX
What beautiful sunflowers, Millie. Thank you for sharing them with me
I think from reading other threads that you are struggling with your treatment plan and have some spine pain. I do feel for you. I hope you can find a good way forward but maybe one with less drastic consequences than I faced!
Lots of love
Daloni xxx
Hi ,
I saw that you were up and posting and thought that I would say hi. Hopefully the hospice is not as regimented as the hospitals are and they let you wake up a bit more naturally rather than coming around to wake you to take your blood pressure.
The weather is not so nice here today but it is dry so far so I might get out a bit later.
I also saw your post about your lovely friends travelling to wave at you from the road. What a lovely thing to do. When the weather is warm again can you get your bed put next to the hedge or wall and chat to your friends over the boundary or it it too high?
You have managed to convert me to audio books but as I am a quick reader don't they take so long? I can read the book in about half the time that it takes them to read it out. I either have to have something that I can do without thinking about of else write off the time when I am listening to the book. It is tempting to increase the speed but it is difficult to take a crime thriller seriously when it is being read by a chipmunk!
It does mean though that when I go on holiday and just want to lounge about watching the world go by that I have the choice of about 50 books to listen to whilst I am doing so.
Wishing you all the best,
Love and hugs,
Gragon xxx
Hi Gragon
I laughed out loud at the chipmunk reading the crime thriller. The beauty of audiobooks for me is that they free my hands so I can, for example, crochet. But these days and with the drugs I’m on I am finding it hard to read very much. It’s easier listening. I think there’s room for both and times we want to bury ourselves in a physical book, times w want to watch the world go by.
Xxx
Hello daloni, I just saw your post inquiring after dizze. I think she replied to you via a Cancer mum post.
I can't find either post again but she was talking about hospital being an alcohol free zone meaning she couldn't toast you so I think that's where she is. Her post was 19hrs ago. If I spot her post again I will reply to it. Xx
Hi , dizzies post at the bottom of page 2 in this discussion.
Take care KT
Hi
Aha! There you are. I do know friends whose visitors have brought champagne but it’s not for me I’m afraid. The epidural delivering diamorphine direct to my spinal cord is doing a grand job. I’m completely free from pain and yes, in a dreamy state.
The nurses here are amazing. They do wake me through the night to change my position so I don’t get pressure sores. I try not to be grumpy when I’d really rather sleep.
Right. Back to the land of nod. Sleep well. Gentle hugs for you too xxx
daloni xx
Dear Dear .
I had hoped that you would like the sunflowers.
In fact, all my neighborhood like them. A few of my dear neighbors are going to get a head of seeds to cook and eat or plant. The girls and I will package some non-cooked ones up for seed gifts for Christmas.
My back pain is just a pain in the back. Seems that my treatment is causing thinning of vertebrae which were no prizes to start with- osteoporosis runs in the family. Just got back my CT and there are no new vertebrae fractures and no lesions on the spine (which was my greatest fear). Just messed up vertebrae and disks. "My back is trash"- has a ring to it huh? Anyway, some nice drugs were given to me to help with the pain.
Waiting for a radiologist friend of mine to do a QCT strength measurement from the CT scan which will determine if I stay on treatment. If vertebrae strength is low then no mas. So, like I said -its just a big pain in the back. And I think some (like my primary care and my oncologist whom I both love) might think me a difficult patient. I think my good way forward will be to stop MCL treatment and manage the pain. We will see.
Still cannot lift more than 10 pounds it makes vigorous gardening difficult but not impossible- luckily I have raised beds like tvman2. Waiting to see tvman's poly tunnel, so I can copy him.....
We did put up nice lights on the patio (posted on gardening 2020) that makes the outside sparkle at night when the family comes over for dinner at appropriate distance.
My dear, I'll go for now, just wanted you to know all is OK with treatment and managing the pain is working, I think of you often. Below is a geography quiz. What part of the world are you looking at?? That might keep you busy for a minute!
With Hugs and Love
Millie
Whatever cancer throws your way, we’re right there with you.
We’re here to provide physical, financial and emotional support.
© Macmillan Cancer Support 2025 © Macmillan Cancer Support, registered charity in England and Wales (261017), Scotland (SC039907) and the Isle of Man (604). Also operating in Northern Ireland. A company limited by guarantee, registered in England and Wales company number 2400969. Isle of Man company number 4694F. Registered office: 3rd Floor, Bronze Building, The Forge, 105 Sumner Street, London, SE1 9HZ. VAT no: 668265007