Both. I'm my (demented) mom's health care Power of attorney. She's in a nursing home and whenever they want to do something to her, they have to ask me first. She wasn't eating, so the Dr wanted to put her on a feeding tube. I said No. He said, "you're killing your mother" I said, "It's time for hospice care". A few months later and she has to get off of hospice care -- for failure to die. She started to eat again. On her own. And the mean Doctor didn't make a penny off of her. and she's not on a feeding tube -- which would have been very expensive. |
Good for you. |
My dad said the same thing. He wanted to pay for round the clock care to stay at home. But I would still have been responsible if they didn't show up or he needed to go to an appointment (which he had many). I had to take on all of his bills and financial needs. This was very time consuming, getting access to his money even with all of the right documents. He lived in N.VA, while I lived in MD. I was working full-time and had two kids in HS. I made the decision to move him into assisted living closer to me. I had to consider my needs in this scenario. Luckily he had severe dementia and thought he was staying at a hotel. Maybe I am selfish but I did what was best for all of us. |
Good for you, PP. Fk any doctor who would say that to a patient's family members. |
Having been through this with my mother in law, I feel the need to share that what people say they “want,” under these conditions, is like what a young child wants. Their brains are no longer able to make appropriate choices. Children “want” to jump off of the top of the jungle gym to see if they can fly, but we stop them. It’s so hard to overrule a parent’s choice, but we have to when they are not in a state of mind to make a choice. My mother in law was living in real filth, eating spoiled food, and leaving the house to wander. We could not take her opinion into account anymore. |
With dementia? |
There’s so much to it. Read the book “Being Mortal”. Part of the issue in modern times is that we have medical treatments that can keep people alive for longer than they would have lived in the past, and a real modern reluctance to talk openly about dying and accept it as part of the circle of life. |
The responsible thing to do in that situation is that she moves in with you. Hard as that is. |
People get dementia who have had no life threatening health events ever. Are you suggesting no one take care of a parent with dementia and hope they do something dangerous like burn the house down as the natural order of things? So what if the neighbor's house also catches on fire? OP's mom needs supervised care. |
The stress he had of taking care of her himself obviously worn him down. In a facility, she could have been in dementia/assited living and him in independent living. They could see each other daily, but he would have had downtime to not be stressed and worried about what she would do to herself or others. If you can arfford it, I highly recommend it |
THis 1000%. People with dementia are a danger to themselves, but also everyone around them. they can burn down the neighborhood, randomly walking outside they could get hit and the poor driver who has to live with that (because they randomly walked into the road and driver could not stop). Key is to get them into a facility early on, while you can still "reason with them" |
Of course you have to consider what is best for your family as the primary caregiver/person responsible for a parent. It is typically much cheaper to be in a nice nursing care/demantia care facility, and also safer. Care is guaranteed and you don't have to adjust your schedule at last minute when someone calls in sick. You have your own immediate family and your first responsibility is to them and yourself. |