Hospice Care
Posted: Thu Dec 04, 2014 11:51 pm
Rose mentioned hospice care on another thread. Rather than clutter and confuse that thread, I opted for a separate thread. My name is Patricia Morgan. I'm a licensed practical nurse in the state of Colorado. I've worked in the medical field since 1992. I've seen a lot of changes. Medical care has gradually become more person centered, and less outcome centered.
When I trained as a nursing assistant in 1992, we were taught how to syringe feed people who didn't want to eat. Today, that's a violation of patient rights, and can lead to assault charges. We also used to forcibly take people to the shower room for bathing. People who were reluctant to take their medication had it masked in pudding or applesauce. Families weren't consulted. The worst practice though, was the overuse of restraints. The restraints were more for staff convenience than for patient safety.
Death with dignity and end of life care were unpopular topics at best. We were supposed to be focused on keeping people alive. Supporting people to have a calm and comfortable death just wasn't what medicine was about. "First do no harm," was trumpeted. But how much harm were we causing people and their families by staving off the end product of life. Then cam advance directives and "Do Not Resuscitate" orders. If I remember correctly, these ideas had to be forcibly pushed through legislative bodies.
Now we have states moving toward allowing physician assisted suicide in cases of terminal illness. I agree with that idea. When my daughter's Aunt Carol died in 2001, she was medically indigent. Physician assisted suicide wasn't even on the horizon, and hospice care wasn't even available to her and her family. Ovarian cancer is one of the more painful ways to die. And since she was allergic to morphine and medically indigent, Carol didn't even have the option of adequate pain control.
Hospice care puts the end of life decisions back in control of the patient and family. Which is where it belongs.
Cat
When I trained as a nursing assistant in 1992, we were taught how to syringe feed people who didn't want to eat. Today, that's a violation of patient rights, and can lead to assault charges. We also used to forcibly take people to the shower room for bathing. People who were reluctant to take their medication had it masked in pudding or applesauce. Families weren't consulted. The worst practice though, was the overuse of restraints. The restraints were more for staff convenience than for patient safety.
Death with dignity and end of life care were unpopular topics at best. We were supposed to be focused on keeping people alive. Supporting people to have a calm and comfortable death just wasn't what medicine was about. "First do no harm," was trumpeted. But how much harm were we causing people and their families by staving off the end product of life. Then cam advance directives and "Do Not Resuscitate" orders. If I remember correctly, these ideas had to be forcibly pushed through legislative bodies.
Now we have states moving toward allowing physician assisted suicide in cases of terminal illness. I agree with that idea. When my daughter's Aunt Carol died in 2001, she was medically indigent. Physician assisted suicide wasn't even on the horizon, and hospice care wasn't even available to her and her family. Ovarian cancer is one of the more painful ways to die. And since she was allergic to morphine and medically indigent, Carol didn't even have the option of adequate pain control.
Hospice care puts the end of life decisions back in control of the patient and family. Which is where it belongs.
Cat