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(I copied this link for u)
https://www.t-mlaw.com/blog/post/avoid-disagreements-between-your-power-of-attorney-holder-and-health-care-proxy/
"Avoid Disagreements Between Your Power of Attorney Holder and Health Care Proxy".
Mum has been very clear in documenting what she would want to be done if she were in your father's position. My Step Dad was clear in documenting what he wanted too and Mum found this to be very helpful when he died 10 months ago. He had children, but Mum was the Healthcare Representative and her word stood.
So in your family, the medical POA comes first. And her first concern should be your Dad's comfort.
It can be incredibly hard for some families to accept that a family member is going to die. I have an aunt who would try to stop the nurses from administering morphine to her husband, as she thought they were killing him with it. She could not accept that the cancer that had metastasized to his bones was incredibly painful and he needed the morphine. He was dying, nothing could change that.
Have any of the doctors explained the level of "some brainstem activity"? I'm only vaguely familiar with this from my father's long-term illness and recovery, but I did spend some time watching the monitor when he was in an induced coma. And it fluctuated, rising so I'm told by the nurses when I sang to him. They said there was clear evidence of response.
I find that somewhat miraculous and inspiring, that someone in an induced coma could tell when he was being serenaded.
Regardless, I think that getting a good sense of what the prognosis is, on a more detailed level, is the first step to making any decision.
As to LTC facility, there are also LTC hospitals, where vent weaning can take place once cognition has been re-acquired.
You don't address the reason for your father's unresponsiveness. Did he have a stroke? Something else?
If it's any consolation, it's worth getting all the information you can, and quietly discussing it with the family, especially your mother, regardless of whether or not she has legal proxy authority to make decisions. After all, it's HER husband, and she's probably closer to him than any of the siblings. She deserves a right to be heard.
And, if it's also any consolation or inspiration, my father was in an induced coma for weeks, gradually came out of it, then spent the next 6 months in LTC hospitals going through vent weaning and dysphagia treatment, and eventually transferred to rehab for a month, then came home with me. He lived another 14 years, productive years except for the last 2 which were challenging.
And this was despite having been told by a pulmonary doctor and an ICU nurse that he would never walk again or live to get out of the ICU. He showed them!
Did dad also have a living will? If not, are his desires well known to you and your family, including the POA? Is there a disagreement on how to proceed?
Hopefully your family can talk this through and come to a decision but it ultimately the final say will lie with the sister with the POA.
Almost 3 years ago my dad (73) was in a similar situation. He'd had a stroke, only brainstem activity, we knew he would never want to live on a machine, he had a living will, so the next morning we had everything turned off and a few hours later he took his last breath. Mom was in charge but my sister and I advised her and we were all on the same page.
Again, sorry you are dealing with this. I hope your family can come to a quick and amicable decision on this.
I am so sorry that during this very difficult time your family also apparently has some division over your father's care. Please remember your father had a reason for naming your sibling POA, maybe the spare your mother the pressure of making high pressure decisions in her advanced years. The POA document may also contain end of life directives, like not wanting to be kept on a vent for a prolonged period. Or your father may have verbally given direction to his POA. My parents had differing directions: my father wanted life prolonged at all cost and my mother doesn't want vents or feeding tubes if she was already terminally ill or wasn't expected to recover. I'm not sure there is a "right" choice, there is only the choice the person wanted or would want if they could still make their own decision.
I can only share being the POA is a very difficult road, full of self doubts, guilt, and second thoughts. The POA is not responsible for the events that resulted in your father being ill and is most likely doing the best she can when making difficult choices. Please try to not take out your own anger, frustration and pain over your father's health issues on your sister. Consider carefully before any steps that could fragment your family for years to come.
Brainstem activity is usually basic control of breathing etc. If there is no cerebral brain activity via EEG in essence your father may be clinically dead. The ventilator is breathing for him. He may or may not be able to be weaned off the ventilator but it sounds like after 3 weeks his brain tissue is dead from lack of oxygen and even with brain stem (cerebellum) activity it appears from your post he has no cerebral function. We don’t know the background here (age, why in a coma now, etc) but that’s my educated guess.
This is a difficult time for you, I know, but your father chose your sister to make those decisions.
I hope you all can come together to support each other.