Fancythat I can fully understand uour comments. Where I live the same happened last year. My DH was nearing end of life, I was caring for him at home on my own. Visit from OT with regards equipment to help. Shiwer seat too big for shower, table for bed couldn't fit underneath, bed raiser could only be fitted at 8 am as 2 man job and drivers left depot at 7.30 am (when DH was in middle of pain control meds) couldn't move, never mind get out of bed, so never fitted. Wheelchair, after I had pursued how to get one had to be measured by district nurse. Who? Where do I contact? Never seen one! Eventually found located at GP practice. When booking appointment was asked if I had a measuring tape as this was needed and she didn't have one to bring with her. When wheelchair eventually arrived, far too heavy, I couldn't lift it. Contacted service who advised they could provide lightweight one. Marvellous, no. Replacement arrived, exactly the same as other one. I had to search to find one I could hire and lift. Palliative care medic visited, she asked how things were going. As I couldn't lift my DH without causing pain she suggested going to hospice to help manage pain. Probably take a week. 40 mile round trip. Staff asked if I was ready at home for his return. No mention of any carers. I asked to speak with Dr who when I questioned how quickly someone coukd be at house to adjust pain meds, say 15 mins, answer was, unlikely. Therefore, my DH remained in hospice for 3 weeks until his death. The Hospice closed last year as emphasis is now on care at home. The only investment in the system, in my cynical view, is not in care staff but in more managers.