POLITICS AND END-OF-LIFE ISSUES
Each day that I walk through the doors of the hospice where I volunteer and enter the warm, peaceful atmosphere inside, I am angered by the Republican attempt to derail health care reform, preying on the fears of the elderly by lying to them about end-of-life discussions. For one thing, it was never suggested that such discussions be mandatory, only included if a senior wants them. But more aggravating to me is the pernicious idea that such advance discussions are a bad idea, leading to euthanasia of the elderly.
I’ve had an advanced directive on file with my health provider for well over a decade – Kaiser requires you to state what procedures you want or don’t want in order to keep you alive when you go in for surgery. I see nothing wrong with it being MY choice whether I’m hooked up to machines that do my breathing for me, or being endlessly resuscitated only to continue on as a vegetable in a sterile hospital ward, wasting my family’s money and emotionally draining them too.
What I’ve learned in almost five years as a hospice volunteer – where you’re asked to make those decisions upon entry, or have a relative with power-of-attorney make them for you if you’re unable – is that the overwhelming majority of patients are happy the issue is settled. Some come to us from a hospital where “heroic efforts” were made to prolong a life that was obviously terminal. (I don’t blame doctors here; their training and their mission is to save lives.) But at some point, our lives are over and to my mind it’s better to face that fact and make sure the remaining days or months are calm and peaceful – and pain free.
In hospice, a patient gets palliative care; by and large, that means as much or as little painkilling medicine as the patient needs or wants. Some opt for less, dealing with a little pain so they can stay conscious to talk to relatives, achieve reconciliations, settle outstanding matters. It’s their choice! In addition, they and their families get all kinds of support from the staff, nurses, chaplains, social workers, and volunteers who have the time to listen to stories and even take the more ambulatory patients on outings to the park or the mall.
Wells House in Long Beach, where I volunteer, has two resident cats, visiting greyhounds (mine), musicians who play “Oldies” at lunchtime every Thursday, or a DJ who plays Rock and Country outside on the pleasant patio, a Karaoke afternoon, and birthday parties for the residents. And the promise that when the time comes your end will be a peaceful transition – and you won’t be alone.
What’s wrong with that? If the health-care bill will pay for more people to have that discussion ahead of time, then it’s beneficial to my way of thinking.
I’ve had an advanced directive on file with my health provider for well over a decade – Kaiser requires you to state what procedures you want or don’t want in order to keep you alive when you go in for surgery. I see nothing wrong with it being MY choice whether I’m hooked up to machines that do my breathing for me, or being endlessly resuscitated only to continue on as a vegetable in a sterile hospital ward, wasting my family’s money and emotionally draining them too.
What I’ve learned in almost five years as a hospice volunteer – where you’re asked to make those decisions upon entry, or have a relative with power-of-attorney make them for you if you’re unable – is that the overwhelming majority of patients are happy the issue is settled. Some come to us from a hospital where “heroic efforts” were made to prolong a life that was obviously terminal. (I don’t blame doctors here; their training and their mission is to save lives.) But at some point, our lives are over and to my mind it’s better to face that fact and make sure the remaining days or months are calm and peaceful – and pain free.
In hospice, a patient gets palliative care; by and large, that means as much or as little painkilling medicine as the patient needs or wants. Some opt for less, dealing with a little pain so they can stay conscious to talk to relatives, achieve reconciliations, settle outstanding matters. It’s their choice! In addition, they and their families get all kinds of support from the staff, nurses, chaplains, social workers, and volunteers who have the time to listen to stories and even take the more ambulatory patients on outings to the park or the mall.
Wells House in Long Beach, where I volunteer, has two resident cats, visiting greyhounds (mine), musicians who play “Oldies” at lunchtime every Thursday, or a DJ who plays Rock and Country outside on the pleasant patio, a Karaoke afternoon, and birthday parties for the residents. And the promise that when the time comes your end will be a peaceful transition – and you won’t be alone.
What’s wrong with that? If the health-care bill will pay for more people to have that discussion ahead of time, then it’s beneficial to my way of thinking.
