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It would be very difficult to take over care for your mother. You would destroy your relationship with your father and even with 24/7 caregivers, you would still need to be incredibly involved in her care. It isn't easy, trust me, I was in the same position in my late 20's. I think you are right that it is your Dad's responsibility and if you haven't been living his life and caring for your mother, you don't know how he is feeling. You don't know what he has been through, the stress of caring for someone and watching the person you love decline for years.

I think the only thing you can do is note all of the mistakes the caregiver is making. Ask your mother's sister to help keep track of everything that is not up to standard. Once you have the detail, present it to him with another solution. It sounds like you have tried that but I would try again with even more specific examples and solutions. However, he doesn't have to make any changes and you need to either accept that or fight it, which will be difficult for everyone, including your mother.
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lovingchild95 Jul 2022
Thanks, yes we have been doing that. Again, he just puts his head in the sand, doesn't want to here, doesn't even want to speak with me on the phone anymore, email only. It's very sad. My mom cries and asks him to come home but he ignores and pretends he didn't hear. Thanks for not being a jerk a lot of people have been replying to me in a vicious manner it's very hurtful.
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nm

Others have already address all I said here.
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If you want to comment, please read my replies to the other answers first.
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That your mom is having 'fainting spells' means that she needs a higher level of care than what can be provided for at home, ie: Skilled Nursing or Memory Care Assisted Living, at the least.

Highly doubtful with regard to 'nefarious plots and elder neglect' considering your mother is given 24/7 care IN HOME which is super expensive by anyone's standards, whether you agree with the quality of that care or not! You are on 'study abroad' and not even on site in person to witness what's actually going on. How would you 'legally take over the responsibility of mom's care' being so far away??? igloo has given you wise advice in that arena.

In any event, in my opinion, your mother belongs in a higher level of care at this point in her illness. Or to have an LPN in charge of her care at home.

Good luck.
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lovingchild95 Jul 2022
Yes, agreed, we need more skilled care in home. That's what I was trying to say. So what do I do if my dad refuses to go with the better caregivers and insist that "adequate" is good enough. I don't want good enough when we have the insurance and there are better caregivers available at the same price, covered by the insurance.
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So dad has and is arranging for & paying for your mom to have some sort of 24/7 care and oversight now for years to accommodate mom’s needs due to Parkinson’s. Is this accurate??
if so, Imho, no way he could ever be considered neglecting his wife; he is imo going above and beyond in doing what needed to have his spouse continue to be in their home. That he has a gf or has a social life outside the confines of your parents home is his decision to make. He does not have to become a caregiving martyr to appease anyone.

Your parents situation in that they have the ability to afford and sustain a stream of in-home $$$$ caregivers is beyond fortunate. That dad has done this for years and years is beyond fortunate. Personally I think you’ll be hard pressed to find a lot of sympathy for your concerns. Yeah I know this sounds harsh but for most couples when 1 needs that level of 24/7 oversight care they end up having to impoverish the at-need spouse and have income go as a copay to a NH and apply for LTC Medicaid for the NH spouse. This is what JoAnn aptly posted about. Most Families do not have the $$$$ to have years of in home caregivers to the point of complaining that 1 of the caregivers sits mom in front of the TV too much.

As your parents are married, your dad as the well spouse is in charge of moms care. He has inhome health happening, he is being responsible. If he does respite, that’s his decision. Realize that regular respite is a given under Medicare hospice so doing respite is encouraged. 4 months is longer than what most do, but if her has 24/7 oversight and is readable as ended, well good for him.

For you to change moms living situation would mean that someone else - her Sister or a grown adult child - would hire and attorney to seek a Guardianship or Conservatorship over mom. (You probably would not be named as you have recent history of going and living aboard for months on end). Atty would file for a Guardianship hearing and your dad as her husband then contests it. Doing this will have costs, and costs that you, your siblings or your Aunt would have to front. I’d say at least 10K as upfront retainer. Your dad can use the $ he & your mom have to pay for his (their) attorney. Please realize Judge does NOT, again DOES NOT, have to name your family or your Aunt as the new guardian. Judge may decide as there’s competing family interests so will name an outside court appointed guardian and that person is now in charge of all moms care and her share of their joint assets and will move mom out of the home and into a facility. That new appointed guardian will move her to a facility as its a neutral space. As your parents are married, the court appointed guardian will be working with dad in some way in all this. You & your Aunts outside of the guardians advisory circle, guardian may meet with you but decisions not yours to make.

Parkinson’s is a cruel dehumanizing disease. That your mom is declining and it’s scary obvious is what Parkinson’s does. It is not ever going to get better & could get worse if she starts to exhibit Lewy Dementia as that often happens with end stage Parkinson’s. (My mom had Lewy). When you return after living abroad for 6 months, you’ll likely be gobsmacked as to how she looks. I’d suggest that you join a Parkinson’s support group now to help you with the reality of what the situation is. Being pissed at dad, causing friction with him, the caregivers and his gf, will only estrange you from your mom in her final years and your dad & his world in the future.
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lovingchild95 Jul 2022
Long-term care insurance covers all of the in-home care. Also I think you missed the point with my concerns, maybe my standard of care for my mom is higher that a lot of people who dump their aging parents in a care home... After 5 years since diagnosis she's been more and less active, after 3 weeks under the care of the caregivers I see as subpar she had the beginnings of a bedsore. That was the first time that's ever happened. The caregiver hadn't noticed or had failed to mention, my aunt caught it and bought appropriate cream to head it off. She's lost weight under their care as well. From her normal 125 to 112 also in a matter of 3 weeks. Still think I'm complaining over something I should be grateful for? Or however you framed it...
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In facilities aides and nurses cannot cut toenails or fingernails because of infection. Just takes a little snip where blood in present, and infection can set in. Medicare will pay for a Podiatrist to cut toenails, but not fingernails. I think the aid can file them but not cut.

You could have APS do a well call for you. Maybe at this point Mom should be placed in LTC. Dad can have assets split and Moms half would be used for her care. When the money starts to run out, Dad applies for Medicaid. He can remain in the house and have a car. He may lose a little in the beginning but he won't have to worry about paying for the constant aides longterm. He will probably be able to keep his SS and any pension he has with Moms SS going towards her care. That will depend on how much Dad needs to live on. He should talk to an elder lawyer well versed in Medicaid.

You need to approach Dad as this will be a win win in the longrun for him. Mom will be safe and cared for in LTC. He can go on with his life.
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lovingchild95 Jul 2022
She's not that far gone! She still can carry on a conversation, if slow, and she's lived in the house for 30 years. Familiarity is the only thing that keeps her grounded to reality. I'm a bit shocked you would so casually suggest we put her in a home and move on with our lives. She may be "safe" but she wouldn't have anything that brings her joy, like her neighbors who stop by and say hi, the garden she loves and used to tend, the afternoon sun in her bedroom. I'm talking about quality of life, not survival.
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