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Nasmir, I am sorry for your loss of your wonderful Mom, I really do understand, as I've lost both of my wonderful parents too!
But you keep going back to it being your "Mother's choice", but just who was going to be there, to care for your Mom, 24 hours a day, you? For our Loved Ones with Dementia and other debilitating diseases and decline, its not always possible for a Son or Daughter to take on this exhausting task! My parents had other horrible illnesses that took their lives, but I have been caring for my FIL, in our home for the past 13 years, and quite frankly, we are completely beyond burned out, caring for him, as he has battled through Lymphoma, and general age related decline. He is a Narcissistic, and is extremely difficult to care for, and my husband, his Son has dealt with a lifetime of FOG, FEAR, OBLIGATION, and GUILT, which is a horrible situation to be in, causing you to be resentful of them robbing you of your life, when they themselves have mentally abused you for your whole life, and he never spent, not even One Day ever, caring for one of his own parents!

I wish you would try to put yourself in others shoes, who have exhausted all other options for caring for their folks, and NEED the family to be on the same page, in further seeing that their parents get appropriate care. And you are right, no Nursing home is like living in a loving family environment, but sometimes, there is no other way!
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Well I am going to ignore the stupid answers on here because a diagnosis of dementia is a solid indication that a person may not have the ability to make cognitive decisions. I only say MAY because dementia is sometimes diagnosed very early on. My mother can make choices for sure but she isn't able to rationalise why or the consequences of her choices so they are NOT decisions.

She also can't make decisions that exist in todays world. When I told her that I had given her grandson a toy she asked how much it was...money being a real issue for her. She went ballistic when I said it cost (in US money) about 17$ said I was wasteful.

This is the same woman who then went to church and gave them all the money as in her purse (at this time I didn't know the problem) some 200$ in your money and then complained someone had stolen it from her!

My son was in denial about Mums condition until he spent some time (a few days) in her company and realised that she wasn't 'quite all there' Mum has perfectly lucid days but not perfect as in normal. Perfectly lucid as in she knows she has to wash and to get dressed.

I think what you need to do Nelsonjosie is to sit your brother down and explain dementia to him and get some print offs from this site to help him understand the path dementia takes and that now you have to act to a) cover the costs of care and b) get the most money you can for the property unless you could rent it out which might be another option

Then once you are talking explain that taking your mum back to the house is not helping and that he needs to take Mum to visit places she used to go to rather than the place she lived in instead. She will forget and unlike other ridiculous comments she cannot make these decisions now as she doesn't understand the associative implications of that decision
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Nasmir Depression IS a mental issue and a very serious one at that

It can be incredibly debilitating
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Nasmir, I'm sorry, but "going to these places " probably did not cause your Mom to further deteriorate and pass away, her frail condition, ilness, and the continuous downhill spiral, was probably the issue, and for that, I am sincerely saddened by. It was through No fault of your own, nor probably the facilities fault, just an unfortunate symptom of getting old and the disease processes thay are declining from. It doesn't matter if the facility was 5 star or less, I'm sure that they did see that she was always fed and clean, and beyond this, it is often the case that they begin into the Failure to Thrive category. It really is Sad, but we All do Eventually Die, and having witnessed 3 of our parents pass away, the end of each was never easy for them, nor us! Our last remaining parent, who lives with us, is declining rapidly, and despite every effort on our part, there is truly nothing we can do but be supportive, and help him in any way, and to make him as comfortable as possible. Whether he is with us or in a facility, I don't think it will matter, he is 86, and his body is deteriorating, it is what happens in life. I hope that someday, there is an outstanding way to make this transition to the end of living better for you and for me, history shows this is not to be true! We decline, and then we die, nobody lives forever. I do hope that you are not beating yourself up over this, I'm sure that you did the best that you could, with what you had to work with, whether it was financial or lack of options to keep her in your home, but please know, she is at peace, and in a better place.
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Nasmir: I believe that you're referring to a DNR order, right?
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Nasmir, Yes, I understand your frustrations regarding the NH bills, but these thing can and sometimes do take time to has them out! Im hope full that you will come to some sort of resolution to them.
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Nasmir: When you wrote "That's why it can be important, while the person is still cognizant, they write down how they want to be cared for if a memory impairment befalls them," you had to have been talking about the OP. So whom didn't have the DNR; I don't know who "she" is?
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