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Oregon there is an alternative that will give YOU control. Email them and tell them you will send them all an informative email weekly/monthly because you know 'how worried they all must be' and as Bill has so many needs now, it is simpler (Not easier never use easier) for you and better for them to keep them updated and you are doing that to avoid answering individual questions

If they need further info could they email you 1 email between them and you will answer it in the next update. That way everyone has the right information and they all have exactly the same information

Then take a moment and prepare a list of meds he takes and when he takes them and what he takes them for.. Shove that in a draft message and keep it safe. Then once a however often you decide send that along with BIll is much the same except that now:

and then list the changes

Do that every month and you have done your job. Oh and always add this

Bill is depressed now the docs have withdrawn his medication, but I know he would love to see you all. Could you let me know when you will pop by - only for an hour or so - he tires very quickly these days. It would give him such a boost and will give you time to talk with him, before he declines further.

If nothing else Oregon they will never be able to say you didnt keep them informed or offer for them to come see him. And if they do you have incontravertable proof they are lying which may settle you a bit hun.

When that time comes Oregon take a journey to lake Oahe -its a good way away - Dakota I think (Im a Brit what do I know) and watch the suns set and rise over the plains. Look at the huge skies and know he is there for you. Then up into the rockies and see their grandeur and know he is there for you , then perhaps to the grand canyon and see its vastness and know he is there for you, go and see as many natural wonders in the USA as you can and know he is and always be there for you. A love like yours cannot die. It becomes a beautiful memory that we can rely on to be there for us when we are in need
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Just an afterthought if they want to come for lonmger then perhaps dont restrict them to the hour and if you can during that time organise for a carer to be there so you can go out and dont have to see them even
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The scary part about leaving him alone with them is that they might trick him into signing something and then later claim that this is the latest document. It really just depends how desperate and unscrupulous they are. I have a first cousin (dad's side) and an uncle (mom's brother) who have absolutely no compunction in cheating their siblings (both into real estate and uncle also with the restaurant-which failed due to several greedy hands.). My mom's siblings took their mother's (had Alzheimer's) money from the bank, CDs, etc... By the time grandma died, uncle the executor of her will was shocked she had zero funds. Grandma was still sane when my mom was diagnosed with dementia. Grandma would visit mom. Uncle said that grandma left $1000.00 to help for mom's funeral. But all her money in the bank, cd and other financial funds were gone when she died . Mom's baby sister was in charge of the funds. She and older sis have opened their store and it's still open. They both travel yearly, etc...

Just be very careful about leaving him alone. One never knows how far family will go to protect their 'inheritance '.
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Book, dad woupd not sign documents for you. Correct? If he signs for your older bro, then dad has just become his or another's responsibility. Your opportunity to take care of you. And I know how that must be a frightening thought for you, it is me after just four years of caring for folks. And you are at more than 20 years?!
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Parkinsons is a dementia so it is debatable whether he has capacity and without it he can sign what he wants but it wont be valid. You need to have control of the finances and then record all spends - remember it has to be in his interests if you are spedning his money. Might be a good idea ot involve a lawyer just to be on the safe side
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Dad hates older bro. He won't sign anything from him. But my dad has always been a flirt. He would sign anything if you're a female who showers him with attention. Or a male who persuades him that he can buy or sell his land for $30,000.00. That was uncle who persuaded dad to sell mom's land for (I didn't know that dad was going through the beginnings of dementia at the time). Oldest brother is mad at me for not telling him Everything that goes on. He said that the land is worth more than that. This is the bro who lives next door, rarely helped out when dad and I asked repeatedly for her. And admitted to me with laughter when mom died, that he was suppose to be the one to take care of the parents (they gave him the land next door which he built his 3bedroom home and a 2story duplex apartment to rent).

Life has always been scary for me.
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This is the bro who lives next door, rarely helped out when dad and I asked repeatedly for 'help'.
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Oregongirl, big hugs to you, first of all. Did the doctors get back to you with any slightly more helpful ideas than just stopping the antidepressants? What you're going through is hard, and all the harder feeling this pressure from his former family, if I can put it like that.

I want to make a suggestion about that pressure, though; which I hope will help in a practical way. Some of the questions you're being asked are not unreasonable ones, it seems: for example, if your father was in that position, wouldn't you want to know who was nominated to be in control of his affairs? The response "it's none of your business" - which is what even silence amounts to - while it feels very natural on your part, is not likely to make them stop asking, and unfortunately that makes it counterproductive. If the information is confidential, tell them it's confidential. If it isn't, tell them who is nominated - why not? After all, they have no authority to change any decisions which have been made - they will have to like them or lump them, so they might just as well know what they are.

If they then go on to take issue with decisions and harass you with arguments, keep strictly to the single point that the subject is no longer open to discussion. It is settled, it is done, and it is not for you or them to alter.

Communication is the key. If letting them stew deterred them from contacting you, it would be a helpful strategy; but clearly it is having the opposite effect. So instead distinguish between reasonable questions which deserve a reply, and cheeky ones which deserve a raised finger, and then I think you will find the barrage much less overwhelming and oppressive.

By the way, it is possible for these daughters to be concerned about both their expectations, if any, AND their father's welfare. Whether or not they are remotely concerned about you is another issue, and will largely depend on what your relationship with them has been like from the outset. If it has *ever* been amicable, use that as a basis for telling them what positive things you would like them to do. If not, cultivate a professional manner for dealing with them - as though they were a bank or an insurance company or something like that, people you do need to have a certain amount of contact with but wouldn't choose to if you had the option.

Does your partner ever express a wish to see them, by the way?
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Hi, I don't get here nearly as often as I would like, but my Mama passed away 3/5/2015 and I miss her so much. I have been her primary caregiver since her aneurysm and stroke in 12/1988, and I was beginning to believe she would outlive me! She was two years younger than I am now when these unfortunate health issues took her from being fully independent, working full-time, planning her retirement to completely paralyzed on one side, having to learn to walk, talk and live all over again. It was heartbreaking to watch as she strolled on downhill for the past ten years, until she was fully bedridden and entered a nursing home with Stage IV bedsores (thank you, Hospice!). Her worst fear finally came to life--being in a nursing home with really no hopes of coming back home. Our dysfunctional family showed its stripes, too, all of a sudden my siblings being so interested in her, after decades of not so much as answering my e-mail asking them for one day a month for Mother to look forward to seeing them--they couldn't be bothered then. Now my brother wants ALL of my mother's financial records so he can pick me apart and sue me for what the thinks should be rightfully his. OMG, I heard of this happening in families, but never thought it would in mine. Now I have no family, no home within about 6 mos., little income since I retired early to care for Mother, and no support the entire time. Oh well, this too shall pass--when I do!! Take care and love to all of you good people.
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Janetrose, my condolences. I know what's it like to have a parent who was alive, asking (sure felt like begging) repeatedly from family to just watch while I take a vacation? Weekend vacation? Or to just go attend mom's funeral (dad bedridden). Dad and I were mom's main caregivers for about 23 years and yet all my siblings and their kids and grands were going to attend mom's funeral. What about me? Anyway, my social worker's work was able to help me on this. I still have bedridden father who has started through the road of senility. After experiencing mom's funeral and the 'aftermath', I already dread when it comes to dad. This time, it won't be the money. There's dad's house and land... I read your words above and felt for you. Knowing where you're coming from. I'm soooo sorry. One day, karma will visit them. {{{{hugs}}}}
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Janet, I am so sorry for the loss of your mom.

Unfortunately, often siblings often suspect the caregiver child of exploiting parents. It has also happened in my case, and nothing could be further from the truth, and it has been a very long battle. The sibs, I call mine the twisteds want to believe that we are mooching off parents, not paying rent, you name it so feel we should do this job for free.

Who is executor for your mom? Who was mom's POA for financial?
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My brother bought the standing air conditioner for $350. He installed it in his bedroom. I slept in an air conditioned room last night. And I couldn't sleep. Even when it was midnight, I was wide awake. I found out that the air conditioner interferes with the wi-fi.

2 nights ago, we had a small thunder and lightning with rain. This dramatically changed the next day from 100 degrees to 88 degrees. What a difference it makes! Last night, I stood by the sliding door and felt a cool breeze (not the usual hot wind). This morning, I'm sitting in the kitchen drinking my hot coffee with no fan (temporarily in the living room) and I'm not sweating. It's 8:30 am and Everyone is still sleeping... I have 5 full days left before I'm literally on the plane for 20 hours (not including the layover hours).
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Janet Rose my condolences and huge hugs sweetheart - it's not enought that you did all the care, it's not enough that they did nothing, they still want to kick you? Well let em honey but remember that karma comes to us all.

So you did 26 years of care during which time they offered no support and I assume you took some remuneration for this? See a lawyer honey they shouldn't get a bean
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Book are you enjoying yourself? Do you think anything will change once you get back.
Enjoy your well deserved holiday as you earned it.
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Thanks, 57twin. Yes, I'm enjoying myself despite the heat. I love window shopping but bro does not. And when we do go to the malls, we all travel as a pack. I'm just soooo not used to that. It drastically inhibits my spending. It's the same when I visited older sis in Colorado. We go to the malls, and she sticks to me wherever I go.

There was a sign that looked like a railroad sign, an X with "R" on left and right. But I didn't see the tracks. So I asked my brother what does that sign mean (then I did an X with my fingers and said R R). Just as he said railroad, we went over the tracks. I think it's so neat seeing a firetruck sign. We don't have that at home.

Today, we drove to North Carolina to visit The Outer Banks. We parked and walked to the sandy beach. It was so hot. While walking on the sand, my feet sinking into the sand, I suddenly got vertigo. I grabbed the wooden post to stop the dizziness. A few more steps and got dizzy. I finally stopped walking when the dizziness got worse. We were suppose to walk along the sand but couldn't because of my dizziness. On the way back, I told bro that I need to hold him to steady myself. I held onto his tshirt's sleeve. I really don't know why I got those terrible dizzy spells while walking on the sand.

We went to Wal-Mart and I bought the travel pillow/blanket for my flight back. The blanket provided by the airline is super thin. I also bought a very pretty and a bit thicker shawl made of 57% rayon and 43% acrylic. My sweater was not thick enough to protect me from the airplane's air con... Tonight, I will start doing the nasal rinse in preparation for my trip. The decongestant pills will start on Saturday. Then the steroid nasal spray on Monday morning.
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Nothing will change when I get back home. Oldest sis did not get her vacation like me. Dad will do the guilt trip that I abandoned my very sick father. And I'm positive that my nieces will not do this next time. Baby sis and baby bro wants me to join them next year at Florida Disney.
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It's too early for you to give up on a vacation next year.
Picking up Dad for blood labs this morning, then breakfast out and he needs new pants as most he cannot button. Will bring back to my house for a quick garden walk well I will drive us around in the Gator for convenience.
I injured myself last night by smacking my face on a set of grow lights hanging to low in basement and have a massive headache still. Missed the corner of my eye by about 1/2". Light now moved higher.
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I'm.exhausted today I injuries my knee lifting grandpa up out of his wheelchair my back,neck and shoulder ache. Grandpa is not talking to me at the moment we had an argument last night. I take care of him.amd an autistic child. I'm burnt out.
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Angel, it sounds like you need a few days break from your grandpa. Their weight can be so heavy for us. It always worries me when I hear of injured knees, since if they are badly hurt they may always give us trouble. I haven't had to transfer weight very often, so don't know what the best way to do it is. I transferred my father a couple of times, but that was awful, since he would stiffen and push against what I was trying to do. If I had done it often, I would have ended up hurting both him and me.
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ladies ladies you need to be careful....for everyone I have found some free videos for caregivers: mmLearn
Loads of stuff on there
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Well, I'm doing alright right now. I already had a confrontation with great-aunt Y this morning, over the birdcage (she wants to uncover the poor thing early in the morning while it's still asleep; it's cage is on top of the piano, and she's already knocked it off twice in the last two months, traumatizing it I'm sure; so I told her I'd uncover it at the usual time and she started going on and on and I finally slammed my fist down on the arm of my chair to get her to STOP and that of course made her madder; oh well). And then just now she wanted to know where her son had gone. I don't know, except that he has errands to run, but when I told her that she got that mad look on her face like I'm not telling her the truth. I have no clue what she wants, but again, oh well. I'm sure she's already forgotten about it right now; I can hear her puttering about in her room.
She threatened to fire me the other day. This is a new thing for her; a few months back I lost my temper and told her that if she thinks I mistreated her like she says I do (mistreatment meaning, not getting a snack every twenty minutes) then she would jolly well have to find someone else, and she was all like, "No, I don't want you to leave. Why do you dislike me so much? Blah blah." Well, she's always been manipulative like that. But now she's threatening to fire me, although she isn't even the one who hired me. And why did she threaten that? Because I sassed her a bit after *she* got mad at *me* for no reason.
Ah, such is life I guess.
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Ya need a break leah - watch out hun - this is a really tough road and it isnt her its the disease - repeat after me its the diseas I hate. xxxxx Get some respite before you burn out baby xxxx
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Thanks Jude :) Thankfully I only stay with her about 8 hours each weekday, and then I get to go home to my lovely family. Some days are definitely harder than others; today is one of the better days, actually; and usually I wouldn't get that mad about a birdcage, if she had just let it go instead of going on and on about something so trivial.
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Jude....whats the name of the site again that has the videos?
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www dot mmlearn dot org
or www.mmlearn.org if that works!
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3 hr sleep only. Sadness within that in 3 days I will be flying home. I went through this the last time I went to Colorado.

I bought one of those bath sponge with a scrubber on the other end and pre-soaped. I've never used one before. I'm loving it. I don't know the practicality of using it back home with the humidity. Everything gets moldy so fast if you don't have constant air con. I will see if keeping it in the livingroom will help.
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Since bro installed the portable air con, I've been waking up with a pounding headache and backache on the right side. This morning was really bad. When I walked into the bathroom, the headache lowered. I can't handle this as my flight nears. I cannot handle flying with a pounding headache. Bro also has a very very old carpet. The same one that was here when he bought the house. I've told bro that I would like to try sleeping tonight on the livingroom sofa. (Even at home, I get head and neck pain when I sleep on the sofa.)

I saved a yoga exercise for neck/headaches in my laptop. I didn't on the kindle. IPad is recharging. I started taking the decongestant pill and nasal rinse yesterday in preparation for my long flight back home on Tuesday. I will find that video!
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http://www.mmlearn.org/ is the learning site for caregfivers - most of it is free too
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Just wondering....has anyone seen the movie 'Still Alice'? It kind of irritated me that it didnt show more realism (in my opinion) of the caregivier side in terms of suffering (frustration, anger, etc). I think thats as much a reality of alzheimers as anything.
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I watched the movie on the plane and fell asleep at the ending. The movie was on the 'dementia ' person's perspective. I've bought the book weeks ago but never got around to reading it.

There is a book that I had stopped reading (prefer fantasy books to take me away from everyday life) that is based on the caregivers perspective. She agreed to take mom to her home. Found out that the 2 bedroom house was a bit small for 3 people. She wanted to use mom's money to build an extension on the ground floor (bedrooms were upstairs) for mom and her sister refused. So, she gave up her bedroom to mom. I gave up reading it because it was reminding me so much of mom and us... I would give you the book title and author but I'm not home. It's Not an ebook which I would have been able to give you the info.
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