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Oh my goodness, you reminded me of what I am missing in life. My kids keep telling me that I am spending time that cannot be gotten back. I KNOW that! This is a choice I made. Not that I love it. I too dream....I am dreaming of taking a cruise the minute I can wake up and not have to start the day with a tight schedule caregiving plan. I want to rent a little cottage on Cape Cod where I can read some books and just walk on the beach...I want SO MUCH to go back to Israel and take my grandson for a couple of months. I want my grandson to walk where Jesus walked... These are my dreams and they keep me going. I don't have that many years left but I can dream and maybe just maybe I will get to do some of these things. But, for now, I am a care giver to a man I love. Taking care of him has brought me even closer to him. Oh sure I hate the times when he become confused and angry and blames me for things. But, I just keep going. Thanks to all of you.
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Sherrybeth...KEEP a JOURNAL....TWO, one on Personal care and activities and the other on meds that you dispense..
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Sherrybeth All the more reason to have an Advance Directive and Medical POA. I cannot thank this site enough. Due to being on here, I have met with my attorney and have taken precautions that I never thought I would have to do. I am so fortunate to have a Partner who admits memory loss and is so willing to take the help that is offered. Because of his willingness to cooperate, he will receive even better care. It is a shame when someone does not cooperate and ends up being in a place where they could be hurt. My backup on the Trust is people who are not even related to us. A couple with four children. The last child they had - they did intentionally just to name the boy child after my Partner. They have more respect for him than his own children. Because my Partner is not fighting change and his personal changes, he is getting much better attention and care. We must all remember to be like this when it is our turn to need a caregiver... My requests are already in writing.
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Thanks Jude....i will definitely read it!
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Daughter, you are not the only person to feel this way. If somebody doesn't feel like that, they are not honest with themselves.
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I dream of winning the lottery so I cna afford the right accommodation and the right care that will give me some me time so I can be a better carer. And if I ever do that:

I dream of a months respite so I can come and give you all a break for at least one day

I long to feel the sun on my back while i read a book
I want my old mum back (and if there really was any justice in this cruel cruel world my dad too....especially my dad)
I hope I can find some good timesto reflect on when she does pass
I'd like someone just once to say have a day out I will come and look after your mum without being asked
I want friends again.
I want to go out and eat a meal I like instead of cooking ones she likes
I want to have a massage done by a blokey who will be nice to me and not treat me like £$%^.
And I know I will miss having mum in my life but it will not be the dreadful loss that most of you will experience I am sad to say

Today she said I had done something well and thanked me. I cant ever remember her saying that to me so I will cherish that one moment - there may never be another.

We all walk this way but once.....I dream, I hope, I yearn but when all is said and done I know reality is just a wall away.

Keep the faith peeps xxx
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Thank you Countrymouse for acknowledging my feelings and not making me feel guilty
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You won't miss having her in your life, but you will miss her. The person she was all through her life, not the all-powerful energy magnet.

And don't apologise for how you feel! Sending you a shoulder rub for the frustration.
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I want...
I want to be able to go to the store to buy underwear or shoes or something on a whim---like I used to.
I want to be able to take off for a whole day or even a weekend---like I used to
I want to browse a bookstore or library
I want to be able to walk without rushing back home (in case)
I want to be able to spend a day with my kids or grandkids (without having to care for her too.
I want to be able to go to the movies
I want to spend an evening with friends again.
I want to be able to date----DATE???? What's that?
I want to be able to take a nap on a quiet, peaceful afternoon without the time constraints---just enjoying the nothing to do again.
And don't say one day it will happen and I will miss having her in my life---I won't miss it a bit.
Sorry for those who may be offended but this is how I feel
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Sheryl beth you have to read this:

Google come into my world.pdf

It will take you to a site which OK is Australian but it does explain a lot - it is a learning resource and is over 70 pages long BUT it says this:

The general definition of dementia relates to any organic condition where there is an irreversible loss of cognitive capacity and memory, such that there is a decline in a person’s ability to function socially, physically and emotionally over time (Kitwood, 1997, Chen, Foo, & Ury, 2002; World Health Organisation, 2007).

The kinds of cognitive disturbance that occur include:
‘memory, thinking, orientation, comprehension, calculation, learning capacity, language, and judgement.
...The impairments of cognitive function are commonly accompanied, and occasionally preceded, by deterioration in emotional control, social behaviour, or motivation’ (World Health Organisation, 2007).

Dementia as a syndrome relates to at least 60 different disease processes that result in neurological failure (Jacques & Jackson, 2000; Ritchie & Lovestone, 2002). Progressive deterioration in more than two cognitive domains along with behavioural changes, as well as depression and other affective disorders observed at the same time, are primary indicators of the disease (Bozoki, Giordani, Heidebrink, Berent, & Foser, 2001; Koltai, Welsh-Bohmer, & Schmechel, 2001; World Health Organisation, 2007).

This progressive deterioration may occur over a long period of time during which physical ability is maintained but independent functioning is compromised.

At present, there is no medical cure for dementia and treatment focuses on medications that reduce the severity of symptoms and may allay the progression of the disease. In the absence of any cure, therapies and care are directed towards enhancing the lives and wellbeing of people with dementia and their carers.

It is great because it tells you about demetia and the best methods of care for your loved one - IT IS NOT A HOW TO CARE WITHOUT EFFORT read for sure but it does have some brilliant ideas
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Yes im in awe of you all who have gone through this for years and years. At some point i will have to go to court and request guardianship since mom will not agree to leave her home. For now, even though the confusion is getting worse, she would not be deemed incompetent because her house is clean due to a lady that cleans once every 2 weeks, and i do all her shopping, appts, checkbook, etc., and she is still feesing herself. But she calls me and soesnt know why she calls...cant remember anything from 2 mins ago, and is in a fog as she calls it. She is so unhappy and yet refuses to go anywhere with me to get out of the house, and does not believe that she has alzheimers. I go over every other day just to 'check' on things...but the worry is constant. The law makes it impossible for me to force a change so now its a matter of waiting till her mind is clear gone or an accident occurs. It doesnt seem right since it should be common sense that at a certain point, a relative shud be able to do whats necessary to keep them safe instead of waiting for something bad to happen first. I have no help either as my oldest sister passed 10 yrs ago and my other sister is mentally as bad as mom due to strokes and brain cancer. I just want mom to be safe and happy...
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Bless all of your hearts. Im so glad we started with hospice 3 weeks ago. They have really been great. I had no idea. They are very supportive also. I wish we had done this a month ago but the MIL hadn't give up at that point. she fussed so much about having to go to the doctors, one time 7 in one week! So I finally told her if she wanted to go on hospice she could and wouldnt have to go to the drs anymore. she was happy to go on hospice. Even told me to call her GP and set it up. So he told her it was the best idea. I feel so sorry for anyone having to do this for as long as you all seem to have. How do you do it? I am physically sore, my feet, my legs, my shoulders, my neck.... I can't imagine the physical and emotional pain you all have went through. I have come to realize that it is like post tramatic syndrome, you wake up at night and it comes all back to you and then you dont rest well then. we all need a big bottle of muscle relaxers to help at that point. Please take care of yourselves. My husband fuss's if I get a sitter much, says we can't really afford it...but we could. He just don't want to spend the money.
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Mom may not qualify for hospice yet but it is worth having them come in and doing an evaluation. if she has had a sustained weight loss that would qualify her. You may find the support very helpful and having 24/7 help available can be very comforting. Talk to Mom's Dr about mild meds to calm her restlessness and anxiety.you don't have to give them if you don't like the effects. Start with the smallest dose and see how she goes. You don't want to totally knock her out just calm her down.
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Every time I'm ready to give up and ask the doctor to call Hospice she (Momma 94} gets better. Now she is back to pulling her Depends up and staying up a lot more? She is very restless though, if she could walk she would be a big problem. She thinks somebody is coming to see us. She is very anxious always asking questions again and talking more. I am still worn out, now I have to watch her every minute, not knowing when she will be wanting to get up and try to walk again. She fell again May 8th trying to walk. She never breaks any thing yet. She is blessed. The EMT's love her. They wait for our call. She always tries to give them a tip. She makes my husband {73 dementia} worry about her and me. My middle daughter{ we have three} comes everyday to have lunch with her We are working on getting help so that after 4 years we can do something together for the weekend before my husband gets worse. We will stay away longer if possible. One day at a time. GOD bless you all!
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GA, for me to do this for nearly four years now took a very dysfunctional family. I kid you not, my sibs did everything they could to make this as difficult for me as they possibly could. I had to prove them wrong, as it increased my motivation. It started getting really crazy almost three years ago when my sibs reported me to APS for allegedly financially exploiting the folks. Nothing could have been further from the truth. The investigator told me he loves cases like this when two people are well taken care of and there is nothing funny going on with the money. I think sibs may have reported me, hoping I had done something and would run. But, if that is the case it certainly backfired! At that point I had to stay otherwise I would have looked guilty.

But, now I am nearly done here, move to facility is Saturday. It has bee a long four years, but I was able to give them that time together in their home that otherwise they would not have had. I am tired and worn out and ready to find out what the rest of my life has in store for me.
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SherylBeth, I am like you. I have been doing this 6 months, about to roll into my 7th month and I agree that all of these caregivers here is an inspiration to me as well. How you have all done this -some of you for such a long time is beyond me. I sometimes feel like I am dying along with my MIL and hopefully I will get through it as the hospice nurses have told me last thursday they think it will be 2 weeks -a month at the longest. I have such strength sometimes, and sometimes I feel so weak in what we all do. Especially some of the bathroom situations and the agitation that my MIL has especially towards me at times. Ive notice when my husband (her son) is home she is less likely to want me to do every little thing for her-no she never asked him for a thing! Why I dont know. I think she has designed me to do it all for her and dont want to ask him for anything. Anyway, as I read most of your post I can so identify with what your going through as well, and I admire the strength and humor and the loving way you try to handle your relative. I sometimes think I need a little more of that. I appreciate you all posting and giving us all a look at your lives within this hell -at least it makes us all realize we are not the only ones going through this. Thank you all so very much.
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Just want to say...you are all an inspiration to me, reading what everyone goes through daily shows me that we are all doing the very best we can. It is impossible for anyone who is not in our shoes to truly understand the pain and stress we go through 24/7. My mom is still in beginning stages of the disease and doesnt require fulltime care yet but the worry and stress of what is to come and when, and dealing with the neediness, repeating, confusion, and new symptoms appearing is already affecting my mood each day. I see what all of you are dealing with and i have such respect for all.
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I had a really nice day with my Mom today! Her health and spirits are fine this week (contrasted to last week), and she was excited to see my new apartment and to help me hang my artwork. We went out to lunch and then dinner too, I drove her to the food store, than a fun goodwill store, and finally we ended up hanging the artwork. She loves my new abode and is very happy for me. We had about 5 minutes of bad communication and I realized I had reacted to harshly to her. We let the bad feelings of the moment pass and continued on to have a great day! Whew! It feels good to be sharing something positive with her again. Teaches me to remember the good stuff and to be grateful for her health and mind at 94! Quite remarkable.
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Jam I totally understand one day this and one day that....Yesterday started out to be a beautiful day with my partner and continued through the whole day. He was sweet, attentive and thanked me for all I do. My first thought was..."He has been healed"...Don't I wish...So far today, it is quiet...We must be going through a MOMENT here and I am loving it. Soon the other person will return...
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thank you again for your comments Veronica
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57 my mom has taken to doing that just recently the fridge is her fave place and I have had to clean it and disinfect it 3 times this week. Howver today I found her putting soiled botty wipes into her handbag. She is very angry with me but her bag is now in the bin yuk yuk yuk
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dad rearranges items in his room. That is what I look for when i see him. Though he was hiding toilet papet under the bed for 2-3 years now.
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glad - a question or just add a button "ops, didn't mean to do that!" btw, seennnothing wong wit yur poting.
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We never locked mom in her room. We triple locked all exit doors of the house. We have an outside kitchen that used to be a garage and that door was locked too. Our locks are not by keys. You just slide the lock left or right to lock or unlock. Dad installed one above the door knob and one below. Mom had free rein inside the house except access to the kitchen.... even when she was normal, she used to go after dad with the butcher knife... one of my few childhood memories that I still remember. We were "locked" inside the house as with mom. If she really wanted out, she can open the louvers and take one louver out at a time, push the screen (only held by 4clips) and get out. Our house doesn't have one solid window panes. It's all louvers.
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I think we have all done it, reported by just a mistap. And I have reported my own posts as well. A simple question, "are you sure" would be nice and simplify for admin I would think. Then there is my all time favotite, we need an edit function. How hard coyld it be?!
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awwwwww bless Shilo
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I wish they would update their technology and add a question "Are you sure you want to Report this Post?". I hit 'Report this Post' once by accident when I was scrolling or I just touched the screen, can't remember. I have no idea who I reported either. That message just popped up thanking me for reporting...whatever it says.
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You nutter Veronica xxxxxx
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was going to apologize for whoevers post I reported but I see it was mine so does not matter
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Gawoman Mom may be closer than two weeks with that much fluid build up. The "blood' spots you are seeing are indeed pooled blood because her heart is no longer able to support her circulation. The underside of any area of her body will begin to display this dark color. it is called mottling and has a kind of "net" appearance. This is all part of the dying process for want of a better term. Ask about stopping her medications at this point and don't try and feed her if she is reluctant and can't swallow properly. talk to your hospice nurse and ask her to answer your questions honestly about timing. No one can give a certain answer but looking at Mom they will have a good idea and what they think will change from day to day. Ask what you should be looking for and what if anything you should be doing differently. With this amount of fluid build up she may start to retain fluid in her lungs ans white bubbly froth may come out of her nose and mouth. Just put a towel under her head and keep it whiped dry. There is a medication called Levisin you can ask your nurse about. It does not treat anything but may help dry up some of the secretions and make it less distressing for you to see. It is a tiny white tablet that you can just slip under her tongue to melt. Swab her mouth before you give it so there is moisture to melt it. Ask your nurse too about breathing changes. There are many things that may or may not happen but it is helpful if you know what to expect. Hospice should have given you literature about death and dying when she was admitted so read it now to refresh your memory. the moment of death is not usually scary just the decent of a feeling of utter peace. You have done your best and that is all that matters. blessings.
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