GrannyGravy13
I nursed my grandma who had multiple cancers in 1976, she stayed at home with pain relief until 24 hours before she died.
Palliative care was provided and did an excellent caring service.
I nursed my mother in my home until 11 days before she died. She then when into a hospice.
Both fabulous kind women who clung onto life until their very last breath, the thought of them maybe being manipulated by unscrupulous professionals (please don’t tell me that these people do not exist, as I know they do, as does history) fills me with dread.
How many times have we heard elderly people say I don’t want to be a burden to my family ? I have seen posts on GN as such.
No amount of shouty letters will change my mind, I am totally against this bill.
And all the credit to you, and I am glad that it was peaceful and painless. But Hospice places are often not available and some cancers do not respond well to morphine in terminal phase.
So many have witnessed unbearable pain for loved ones, unable to help them at all. My heart goes to all of them. Many doctors and nurses will tell you about so many cases too.
Every step will be taken to ensure no coercion, from family or staff.
However, what is wrong in not wanting to be 'a burden'- in not wanting your ACs taking much time off to hold your hand and watch you suffer, unable to help. I do not with to want to suffer in latter stages of cancer, part of this for myself, part of this to not leave my family with terrible memories of those last stages in my loss of everything over an extended period. And I would not wish for the cost of looking after me in those last stages, to be taken off the budget for those who need it and have a lfe n front of them. What's wrong with that?
(I have checked, and this is totally irrelevant- caps are only considered 'shoutint' if continuous, but totally fine for emphasis of a word or two.)