Hearted Youtube comments on The Japan Reporter (@TheJapanReporter) channel.

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  12. I am a hospice caregiver to my grandma in rural USA. I have to be with her 24/7 because she is bed ridden from a stroke and stomach cancer. I'm very blessed that she is mentally functional for the most part. I also took care of my mother when she had/survived breast cancer. From my point of view, it is important for caregivers to receive more support than we get currently because we can provide a level of care that you will never get in a government funded nursing home. I'm blessed that our hospice staff are so helpful, but having some sort of monetary support for those of us who are giving up our careers, time, and energy is important as well. Especially since this is often a 2+ person job for many conditions. This video brings up the cases of family members abusing or killing the people they are caring for, but this happens all the time in nursing facilities and hospitals as well. As part of our hospice program, we are supposed to get 5 days of respite a month where we send her up to the hospital to be taken care of so the caregivers can get some rest and take care of business. There are two problems with this: #1 we're only eligible if we're unpaid caregivers, even including the caregiver pay system through the government would make us ineligible. #2 the first thing they do as soon as they get her is taking away all her nutritional supplements, drug her up to the point of psychosis, and vomiting out any kind of intake, including water. This last time we had respite almost killed her and we were having to deal with it anyway so we weren't getting rest. We sent her up to get rest. Not for her to be executed. It's taken over a week and a half now to recover to the point of her thinking being clear again, but her appetite and physical capabilities seem to have taken a permanent hit and is speeding her decline. Something that is hard to keep in mind is that the government has a vested interest in people in these situations to pass away as quickly as possible because they are considered a resource burden. It's one of the reasons why abuse in nursing homes is so rampant in addition to how difficult the work can be. As for the caregiver pay i mentioned before. I have a friend who is on that system. It pays alright at 17/hour, but they apparently limit it to 10 hours a week. That might be dependent on the patient's situation since their patient is mobile and only needing limited support whereas my patient is bedridden. I'll be finding out soon since we won't do respite anymore. Sometimes I do get depressed that I likely will never have a family to take care of me when I get to that age where I'll need help.
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