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My mother in law, 93, has had several ER visits, a hospitalization with surgery and a stint at rehab so far this year. Each time she is asked if she has Advance Directives and she always says she does not want to be resuscitated, but we don’t have a formal document. Once in the ER, when they kept her overnight, a geriatric NP brought in a DNR form which my mother in law signed. It traveled with her up to the hospital room but apparently was only good for that one admission. My MiL is adamant about not wanting to be resuscitated, but I know there are other medical interventions to weigh in on in Advance Directives, like antibiotics, IV fluids, feeding tubes. I mentioned it to her one time but she seemed overwhelmed and merely stuck to her one request for DNR. When she had an outpatient procedure recently, the admission nurse asked about Advance Directives and when my MiL claimed No Resuscitation, the nurse said it doesn’t count if you don’t have a legal document. So- we’ve been “meaning to get around to it”, but dear MiL only mentions such things when she is sick or in some sort of medical crisis, which is a terrible time to bring out forms and documents, then when she is feeling better, that also seems like a bad time to bring up end of life choices. I’m probably in some sort of avoidance mode. But I welcome advice from those who have already dealt with this. She has an appt with her PCP in a couple of weeks and that seems like a good time to address the issue. I just want to be prepared. Thanks in advance.

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MaryBee, Part I, the upcoming PCP appointment would indeed be a very good time to raise the subject. You could, for example, say to the doctor "we've been thinking about this from time to time, but could you explain how we can get the job done and out of the way?"

My mother's GP responded to this kind of request by printing off a good, clear leaflet for mother to read in her own time; he stopped short of recommending she get on with it, which he felt would put pressure on her and make her depressed; and he declined to put the Community DNACPR instruction* in place until some months later.

In terms of getting down to the nitty-gritty of IV feeding no, antibiotics yes etc etc etc - you might do better to go for outcomes rather than procedures. So, for example, MIL might like to state that should she experience a health event that does not give her a realistic chance of substantial recovery, she wishes to receive palliative care only; or something like that. If you attempt to be too prescriptive you're begging for trouble in the shape of something completely unanticipated which then refuses to fit into the boxes you've so carefully put together.

But - Part II - you can just let this be. Relax. If it gets done, good, it will be helpful, everyone will have guidelines to follow. But if it doesn't get done by the time the time comes, your mother and her doctors and her family between them will still make decisions in her best interests, and that will be fine as far as the process can ever be fine. It won't make *enough* difference to be worth a painful struggle, is what I mean.

*In the NHS there is a greater onus on clinicians to judge whether interventions are justifiable in a patient's interests or not. So PCPs/GPs can issue a "Do Not Attempt CardioPulmonary Resuscitation" notice which they keep on file, with a copy kept in the patient's home for reference by any health care professionals attending, such as nurses and paramedics. They wouldn't do this without discussion! - but it does mean that they can avoid forcing people to face up to issues they may understandably prefer not to think about.
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When my MiL came to our house back in Nov. Her daughter had PoA but it was not Durable. The Dr's here (in Florida) , set her up with a yellow DNR form, that we keep in a ziplock bag and on the fridge so any health care provider that comes to the house will be able to see it easy. It's the legal document here. They may have something similar in your state, ask your local Area of Aging. They would know.

Her Dr's also set her up with a Five wishes, It's a legal advanced directive here in Florida and in many, many other states. What I like about the Five Wishes, is that it's easy to understand language, it explains what each thing is and you can cross out what you don't want and write down what you do want. In a couple of states it has be notarized but here in Florida, we just needed two non blood witnesses to sign and it's completely legal. Google Five Wishes and you will find much more information.
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Countrymouse, thanks for sharing your insights, especially the suggestion to focus on outcomes rather than procedures. We will bring it up with the PCP.
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MACinCT is right. You don't need the advance directive. Every hospital visit you will be asked and you just keep signing the DNR form.

My DH passed last night. He didn't sign the DNR but I did when he went downhill on Thursday. We have no living wills and managed just fine. He passed at 96 yrs, peacefully in his sleep.
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At the PCP appointment is a fine time ... if the PCP immediately brings out a form she can fill out and sign right there, great. If the PCP doesn't, though, or if the PCP suggests she 'read it over and think about it,' I suggest you ask her to sign a Health-Care Power of Attorney or Health-Care Proxy (or whatever it's called) that makes you the Official decision-maker if she is unable to speak for herself.

I'm glad she has been able to sign the in-hospital DNR each time, but the day may come when she can't. Then, unless you are physically present to stop them, someone will likely start CPR first and ask you about it later.

The best Advance Directives these days focus on Outcomes rather than Procedures, because events have a way of not fitting the check-boxes.

For example, my mom, 89 and frail, was still living at home with the help of my brother. She was absolutely clear that she didn't want to be hospitalized ever again, etc. But then she fell and cut her scalp (which of course bled like crazy) while knocking over the bedside commode. My brother persuaded her to go to the ER for the wound to be cleaned and stitched, so she wouldn't die of a preventable infection. She was afraid to go -- what if she had another stroke? then they would insist on admitting her and starting aggressive treatment which she didn't want -- but finally she agreed, with her Health-Care Proxy document in hand and my brother (the PoA) by her side. The hospital agreed that if her health-care proxy was there they could abide by her wishes.
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Dear MaryBee,

With my grandmother they had a lawyer come to her nursing home to fill out the paperwork. I think all her kids were with her. Good of you to look out for her and her interests.
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Good morning RayLin, I'm so sorry for your loss. But what a great long life your husband had and a wonderful way to pass. God bless, hugs to you.
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MaryBell, I am moving your post back toward the front pages of the forum. Hopefully a caregiver will be able to answer your question.
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Freqflyer, thanks for moving the question up front and Macinct, I appreciate your response since you’ve been through this.
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Since your MIL has problems with the advanced directive, maybe the healthcare POA would be an easier step. The HC-POA can sign the DNR if your MIL is not able and can make those decisions usually covered by an advanced directive too.
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