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Book, let me make a slightly more practical suggestion; bladder sizes vary WIDELY. ( I know this because my husband had his measured recently and the urologist was quite impressed. It holds 20 ounces! Which is why he only has to go once for every 5 times I pee when we're on road trips.

Instead of trying to drink all that water each day, drink a small (like 3 or 4 ounce) glass of water each time you pee. See if that helps.
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Bookluvr,
With g.e.r.d. , drinking large amounts of water can be tricky. I was chug-a-lugging a full 8 oz. at a time, trying to meet the daily quota when g.e.r.d. then became worse.
So Barb is correct, to drink smaller amounts at a time if that works for you.
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Yep. I noticed an increase of burping and.. water coming right back up several times now. Being determined to drink a lot of water, I was ignoring the burps and back flows. Got it...no more big gulps to 'get it over with' but sip daintily..
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Book I drink ALOT of water, always have since my teens when I read it's good for your skin. ( I have great skin in my late 50s so it must work!) What works for me, even with a busy job,, is just to always have a bottle near me. I use a bottle that helps to keep it cool, and just sip away when I think of it, whether I feel thirsty or not. I always take some with my in the car too. It works better then trying to chug a whole glass at a time!
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Now another thing my mother can't understand. That has a simple fix. But she has to make it hard.

In the bathroom next to my bedroom. The toilet's flush arm just broke. I fixed it the last time, AFTER, I told her not to call a plumber. I just have to go to Home Depot to get the replacement part. But she isn't satisfied.

She wouldn't be like this with my younger, able-bodied, Ph.D., married brother.

I just had to get that out.

P.S. On the water topic, I calculated(by the formula provided here), that I would have to drink 17 cups/day.
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When my boss' wife's father died, I struggled to offer my condolences, with trembling voice and trying not to cry. He had Alzheimer. She's from a large family, like me. Yet the sole caregiving fell on the live-at-home brother taking care of their elderly parents. I didn't go to her father's funeral. Just like I didn't go to my oldest sister's 10 year old granddaughter who died from bone cancer. Nor did I go to both of my father's sisters funeral...

When my mom died, my boss said he will see me tomorrow at the funeral. They never came.

When my dad passed away, I knew they wouldn't come. They didn't. How do I feel about this? Disappointed. A bit hurt. Grateful they didn't come because working for them in over 20 years, we have made an effort to never sit on the same table when attending business functions. We have always kept our business and personal lives separately.

Anyway, on Wednesday, boss' wife calls and says she's going to be in late because she's.....{pause}.... going to a funeral...... The boss comes in, sits at his desk and tells me that wife is coming in late because she's.... {pauses} ... has something to do.

Awkward!! Not for me but for them. All of my family went back to work and received condolences cards with money. I got nothing. How do I feel about that? Sigh... it didn't help my case when my longtime client came in with a special thank you gift for coming to her mother's funeral. I reap what I sow. I couldn't go to the boss's wife's father's funeral but I can go to a client's? Karma.

I just mentioned this because I wonder how long they will be awkward about Saying they are going to other people's funerals yet they didn't come to their longtime employee's funeral. ... Guess what, she doesn't know it - but I think we're distantly related. Her uncle is also my uncle. He even gave me a funny look when he came to our office. I look familiar to him and he can't recall why. I recognized him immediately from when I was young and used to attend funerals, rosaries, weddings with my mom. I hoped really hard that he wouldn't recall my face. Ugh! Awkward if she finds out that we're related! Like I said... this is a small island!
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Chris I am afraid your mother is assuming that because you have physical disabilities you are also not very smart either which is obviously not the case. Once a parent labels a child they tend not to change their minds. She may also feel guilty for producing a damaged child. It's strange what things get stuck in peoples' minds and at her age there is no changing her mind. But you can keep in mind that it is only your outside that is defective but despite that you are a whole person and should be treated as such. Mom is very lucky to have you.
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Ohhh. A thought popped up while brushing my teeth... I didn't give boss wife a condolence card. I'm going to have to read up on some tips in every day life because I'm lacking in that department. My parents nor my siblings never told me what's expected of us in certain situations... advice from Heloise! .. time to google...
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Sendhelp, I was always wondering why I would get acid reflux after drinking something as simple as water. Had me totally baffled. Whew, what a relief to know why that is happening :)

Bookluvr, I would need to drink 21 glasses of water. No way that would happen. I can barely finish off one 16oz bottle of Deer Park.
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Book, when there are parents that you care for, attending other funerals, memorials are very difficult. I have never been a funeral attender anyway. And I rarely send cards. My friends here are fortunate to receive my condolences, grimace, maybe because of losing my dad at such a young age? I went to a funeral for the parents of a middle school friend of my son's what probably 15-20 years ago now. They were hit head on in a snow storm by a semi truck. I cried like I have never cried in my life. Memories of losing my dad at about the same age, I imagine.

We all do what we can do, some of us do funerals better than others, I am definitely not one of those people. That is ok. I am ok, because of my own losses, they are just very difficult for me. Remember, I even thought and talked about not attending mom's.

I really do not think when it comes to funerals people develop an attitude that she did not attend mine, so I will not attend yours. At least I hope not.
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Veronica91-Thank you. My mother n' younger brother agree on EOL(End-Of-Life) issues like assisted-suicide, and not sustaining life by medical means. I don't agree with either of those things. My mother's middle cousin on her mother's side agrees' with her. But lives in VA, far outside the DC-Metro region, yet not in the Roanoke region. My brother, SIL n' their kids live in SF-CA. So, If something does go wrong with my mother's physical health, my cousin will have to drive down here. Because she has POA, if my mother is incapacitated. My mother has bullied me several times for not agreeing with her on EOL issues.
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Chris I totally understand your end of life beliefs but maybe you would change your mind if you saw someone you love suffer horribly before dying. Both you and your mother and family are entitled to your own beliefs and opinions. if your mother starts the bullying again just tell her she need not worry you are not her POA so won't have any say in her EOL care. Not that it will stop her she still thinks of you as a child who can be ordered around.
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Veronica91-I saw my maternal grandfather steadily decline, the last year of his life, back in 1975/76. When I was 8/9yrs.-old. He had a 'regular' death from Alzheimers. No assisted-suicide, no cremation. So, I have seen someone 'suffer'.

Two of my mother's (former)Masters students' both died from AIDS. While I didn't see them daily like my maternal grandfather. I did see their respective steady decline. Being cremated was their choice.

That is the key, 'choice'. My previous point about my mother not calling the plumber. Was affecting 'her choice'. But the 'choice' was not life-altering. EOL issues are affected by 'choice' and life-altering. That is why people have(or should have) a Will.

I can't do anything right. In her eyes'.
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I don't know if you guys have read the recent Oregon case for the woman with Alzheimer's. She had advance directives with no extraordinary measures and no forced feeding. She has been in late stage for the last two years in a nursing facility. Her husband is pushing for her right to die, but the decision was against this because his wife was still opening her mouth when someone fed her. From what I gathered her mind has been totally gone for two years except for the food reflex. She has an IV for fluids. Her husband is healthcare proxy, but he doesn't have the power to get them to stop until his wife stops opening her mouth for food or dies naturally. I felt so bad for both the woman and her husband who are trapped in this endless good-bye.
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Jessie, Oregon is one of the very few states the legalized the right to die. From your comments, the woman with Alzheimer has all her documents in order with advanced directives and healthcare proxy. I'm guessing because they signed her up in the nursing facility, they somehow gave it a higher authority over her welfare that trumps all her other documents. They will fight it because she's a steady income client. Moral of the story: before signing anything, have the lawyer review it - that you're not giving up control over your loved ones life to the facility.
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Jessie, As Bookluvr pointed out. That Oregon is one of the few RTD states. Is the woman's mouth continuously moving 24/7? If that is the case. It is sort of like someone who is brain-dead. But their heart keeps beating. Which becomes the kind of loophole in the law.
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I was surprised, too, for Oregon. The problem with Alzheimer's is that by the time you get to the late stage you don't have the ability or competence to request assisted suicide. Only people who know what they are doing and are medically eligible can request it. The advance directives did specify DNR and no feeding tube, but in this case she is still opening her mouth to receive food. They can't legally starve her. She can refuse food and they can't force it on her. It is one of the cases where the law is on the side of continuing life, though the family knows it is not living. I believe the nursing facility is required by law to feed her as long as she is taking food. That is as much as I know about the case. I don't know why she isn't taken home and put on hospice. There must be some reason.
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That was I was thinking - to take her out of the facility and bring her home. Lots of people do that here on island. I know of several people (including my dad's sister) who spent months in the hospital. Finally, they requested that they want to go home. Within a week of coming home, they passed away. I've heard from the their family that they just wanted to die in their own home and not at the hospital. And they got their wish.
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I know that I'm going through depression. It was kind of getting bad the past few days. It's back to having those terrible thoughts. BUT, I have always been self-aware/self-evaluating. I'm Not in any way in a critical condition. Just fantasizing, wishing, longing....

Older sis has always had the 6th sense. Hers usually have to do with dead people's spirits visiting her and alerting her that they've died by odd events - like a loud bang against her wall, or the TV turning on/off, etc... Lastnight, she actually called me. She Rarely calls me in her morning time - especially if it's a work day. She called and the first thing she asked me was - how are you doing? Are you okay? I'm concerned.... I told her that everything's fine but I don't think she believed it. She kept coming back to how we're doing and that she's really concerned.

I've decided to take a course on happiness since I don't know what that is. I grew up from a very dysfunctional childhood where I grew up thinking that it was 'normal' to live constantly in fear, anger, etc... All negative emotions. So, I wanted to learn about happiness.

Today, I took the test on my happiness level.... My results - depression. IF I had scored under 'Unhappy', I would have gotten the recommendation that this course can help me.... Instead for my score level, their recommendation is: "you should consider some professional help (e.g., seeing a therapist.)"

Sigh... No, I will not seek therapy. Been there twice and I've learned that I need to be motivated to do things. I'm a procrastinator and I tend to start projects and never seem to finish it.  Same as therapy.  I'm actually bordering as a hoarder (with lots of unfinished projects that I refuse to throw because one day I will have the desire to complete the project.) Hmmmm. Maybe I need to first find a course on how to stop being a procrastinator. Okay, I'll research it later. =)
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Oh Book, you've had so much going on both physically and emotionally that it's only natural to feel down. Take the course anyway if you want to, it can't hurt and you may benefit from it.
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Thanks, Cwillie. I wasn't surprised with the result. I actually laughed because it was true. Therapy?? I sat here thinking about it. I reread the survey questions. I answered it truthfully. But the questions don't really apply to me because I spent 25 years caregiving. So of course, my life is not close to my ideal, etc..

So, with that aside, and not growing up with hugs, encouragements - this course is perfect for me to learn about happiness and how to achieve it. I totally agree with you about still taking the course.
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Always Hugs for you Book!
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Oh,just another 14 hour work day. Then home , do what dad needs. Maybe sleep 4 hours,do it again tomorrow. If I don't work like this, we have no home.
I'm tired.
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Hi Jenaynay. I remember doing that for years, helping dad with mom. I'm fortunate in the sense that I got 5 hours of sleep.... Most of my life was just home and work. I didn't have weekends free, either. Vacation away from home was very rare - money wise and finding someone to help with the caregiving. When dad had the stroke and became bedridden, I couldn't quit my job. We're not independently wealthy.... I was overwhelmed by it all... I even googled "caring for bedridden parents" and found this website... I vented and vented all my anger, bitterness, vengeful feelings. And most of all, I found support here.

Please feel free to vent. We all know what you're going through in one way or another. I really soooo feel for you. {{{{HUGS}}}}
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Thanks , bookluvr. I have been supporting dad for 7 years now ,he has SS but its enough to pay his bills, not much to help me. The past year has been the worst , had to change jobs to make ends meet, but now I commute 30 miles each way. I'm a chef by trade, so long days are normal. BUT, I'm about to turn 55, don't know how much longer I can keep going at this pace. I do exercise, and eat right.
Dad is in denial about turning 87 soon, I can't seem to get it through his head that he's not getting stronger. Just an hour ago, he dropped the mail and almost fell trying to pick it up. Yelled at me when I tried to help. I am going insane , I feel isolated. No friends want to be around me anymore,i must be a real drag,lol.
So I found this site, and now I know I'm not alone in this struggle. Its been helpful....so has Moscato,lol!
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Jenaynay, I know that you have very limited time to be online. I would strongly recommend that you hop around this site and just read different discussion threads. I really think it's very important as caregivers to protect ourselves. Knowledge is very important. Ignorance is scary. Even if it means just taking 5-10 minutes before bedtime or upon waking up to read different topics here.

When I first found this site, I read everything that I could - even on subjects that had nothing to do with bedridden parents. I read threads about "how can I get my parent to drink more water" or... about their personality changing.... or how vindictive/abusive the parent is towards the main caregiver but very very nice to everyone else... or having problems with bowel movements... Trust me! You will be soooo glad that you've read about it months/years ago.

When my mom was violent and was sundowning (walking all over the place, getting lost), my SIL (sis-in-law) told me and fave sis that we should lock mom up in her bedroom. Sis blew up and they had an argument. Who was SIL to tell us to lock up mom! .. Years later, I found out from this site, that it is illegal to do that. What if there's a fire? Mom would not have been able to get out/escape.... Anyway, Dad's solution was to just put several extra sliding locks on all the exit doors. Mom didn't know how to unlock those.
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SIL texted me, saying that my (oldest) brother would like to have mom and dad's hospital beds. Mom's bed is completely manual. Very, very easy to raise/lower. Dad's own is electrical powered. Mom died on her bed - which everyone knows I absolutely refuse to lie on it. I was torn about this. You see, my acid reflux is getting worse. Using the wedge pillow and more pillows on top - is not working - because my GERD is getting worse. My fault. I have such a difficult time not snacking after 8pm. Drinking water after 8pm also worsens it while sleeping.

After some serious thinking... the lawyer did tell oldest bro that as named administrator of the Will, the heirs should be paying him. But it's up to him to waive the fees. Sooooo... I've decided that I cannot pay bro any fees as administrator... {grumbling...that HE was suppose to be taking care of mom/dad when they were alive - he admitted this to me when mom died...} I told SIL that I would like to keep one bed. They can choose whichever bed they want. They get first dibs. She chose the manual. I asked if she's sure. She's sure. {Thank Goodness! Because if I had asked bro, he would have chosen the electrical one!}
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Book, the way it works is that the executor/administrator is paid by the estate, NOT the beneficiaries. And that is taxable income, so because of that (as well as a sense of familial duty) many people do not accept a fee. You DO NOT owe them anything, and even if you did it would be taken from your portion of the inheritance.
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Cwillie, we, the family went to the laywer. He looked at my brother and told him that he should be paid as administrator. And that it's the heirs who should pay him. So after we left the lawyer, I told bro that I cannot afford any legal fees for the lawyer. That my 2 brothers in the states make more than double my paycheck. I wouldn't even qualify for a $5000.00 loan. So, if brothers won't help pay the lawyer and court fees (the court will only charge a max of $5,000), then bro, as administrator will just have to sell the house/land to settle all monetary debts. Bro was not very happy about that. Remember, he wants this house/land for himself and his grown up children. Selling this place is HIS last resort. As for me, my dad always told me that this house/land will go to my other 2 brothers in the states. If I wanted land, then I should marry a man with land. So, at this moment, I have never really viewed this place as mine. So, selling it is not a hardship for me. It is for oldest bro because he has always wanted this place. He has all his caged roosters on dad's upper land, his dog, and all his broken down cars - all on dad's border. He and his family all park on our front yard. He's been slowing moving his stuff on dad's land for the past couple of years.

The lawyer said straight out that the heirs will pay all costs. Thanks, Cwillie. I will need to keep reminding myself not to put any money for the probate costs. I keep forgetting. I think I need to put a post-it note on my bedroom mirror reminding me of this. Estate pays, not me. Thank you!
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bookluvr, your message made me very sad at how badly you were treated. It is very sad if the women are treated like that. Shame on the men, and even like expecting you to pay something so they can inherit. :'(
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