Double ditto here!!! I can't imagine my taking that on longterm like Deb (altho I know if it were to become necessary I would try but probably fail miserably, except for my DH of course, I have already told him many times he will never see a 'home" as long as I have a muscle left) I also PITY any family member who might try to care for me in the future. I have always been fiercely independent (drove my poor DH crazy when I broke my leg/ankle. I would wait until he went outside to sneak myself in/out of my wheelchair, etc.). Tho I actually enjoy doing things for others, that's probably how I wound up doing the hospice care at three different times for friends/neighbors.
I am, at best, very uncomfortable with people doing things for me, most of the time flat out hating it. Me being forced to depend upon someone else's help? That person would need LOTS of prayers!
You can understand where my parents are, can't you? My mom has always been the caregiver, and now Dad is having to do the caring. In some ways, they are fairly well covered - Mom has had someone coming in helping with the cleaning and yard work for a while now, and Dad has done the laundry for years (my brothers and I are willing to do whatever we can, but they live at least an hour and a half away from any of us). But with her dominant arm out of commission, Mom really can't do anything, and I know that bugs the heck out of her. (Incidentally, she has an appointment with an orthopedic surgeon on Wednesday; we're kind of in limbo until then)