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Another completely kind of fowl?
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Hi Glad! Almost time for bed for a working woman?
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Well FIL is in the hospital ( see other thread) and was doing well, today he is unable to walk and very disoriented ( which he is aware of). Hubs and BIL are not handleing this very well, and really don;t know what to ask, etc. So tomorrow on my day off from MY hospital I will be there playing bulldog. They have no idea if they changed his meds, does he have a UTI.. nadda. And my friends Gma was taken in today with disorientation. Things are going around folks! My mom slept alot today also... The one smart thing home thing I did today was ask hubs to pick up the daughters dog and bring her to our house for the weekend.. Mom loves her and it gets her moving and some company when we have to go see FIL. Wish me luck here folks!!
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Ahhh, Pam, when it rains it pours! Best wishes for everybody, they are fortunate to have you!
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Oh Pam....sheesh. Not like you needed that to happen! Will be keeping you in thoughts and prayers. Keep us posted when you can.
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Thank you both!
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Mom is getting completely slurry with my phone calls to her. I think it's because I wake her up. She gets up at 2 a.m. and she's proud of it! Geesh! Gotta get the girls before they change shifts at 3.

That's just goofy to me but it's her life. Do what you feel you have to do. She makes sure I feel guilty for sleeping until 6 in my life.

But you know what? I don't feel guilty. That guilt went away. I don't know when it happened over the past 5 plus years, but it did.

I never was responsible for my mom's bad choices in life and I finally GOT that.

I will be there for her and am. I see her on Wednesdays and my husband and I take her out to lunch on Sunday. I provide everything for her including evening meals for the naysayers. I also call EVERY day.

I'm 20 minutes away. Just can't see her. it's too toxic.
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First time ever entering a group like this, I am scared tonight because I am positive after tons of research my mom has a major problem ...I think she's losing her memory & tonight I feel helpless. We live states apart & am so concerned I need to fly to see her. I never ever thought she would have dementia or allziemers but it's crystal clear tonight ...I don't know what to do ...
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Hi Mcwattz, the first thing you need to do is a quick research on dementia and the signs. Read stories of people's experiences with their parents, etc... Take lots of notes. If you have a laptop, open up a Microsoft Word and title it with: Symptoms/Signs, another Word file as: experiences from family; another file as Tests, etc... Do what is best for you. No need for any Deep research. Just do it like an outline style. I usually copy/paste the website with the most information onto my Word notes (instead of taking up too much paragraphs).

While you're researching, you will learn what to see when you visit mom, how to respond, etc... BUT, if you don't have time to do research, please Google: Teepa Snow's YouTube videos. They are short videos but very very educational.

Have you seen this topic on the Home page when you first found this site? Signs Your Parent Needs Help:
https://www.agingcare.com/articles/signs-your-parent-needs-help-143228.htm
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Pam, sorry to hear about FIL and all the others who all seem to have a medical crisis all at one time.

Windy, hopefully it's just because she woke up.

Lately, my dad's been slurring his words. Forgetting what he wants to say. I have a feeling we may not be able to get the POA in time. I've stopped panicking about that. If we miss the opening door, then we missed it. I'll just continue to wing it as I usually do.

On my last visit to withdraw funds from dad's account, the teller asked me if we can update the account. If my dad and I can come into together.. I told her that he's bedridden and we cannot even get him to the dentist. She would like dad to put a beneficiary on his bank account. She said that if something were to happen to him, the bank would freeze the account and see who's the heirs. Whereas, if he has a beneficiary.... So, I came home and asked dad if he wanted to put beneficiaries. He said yes. He wants it to go to me and oldest sis since we're the ones taking care of him. {{rolling eyes}} The bank will be calling me on Monday with all the updated information. Then we will set up a time where i can be home and have a phone conference with them so that dad can confirm that he does want to have a beneficiary for his account.
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{{grumbling}}} if we were both taking care of him, why can't she change his pamper or help me with it? Or when he spills a whole glass of water on himself or on the bedding, why doesn't she change the bedding and his clothes? I usually find him soaking wet when I change his pamper at 9pm. He's been hours on that wet bedding /clothes. He would spill on the floor and she doesn't clean it up. Do you know how difficult it is to wipe up spilled almost dried milk on the floor? Sticky, too! Sorry... venting again. I'm really trying not to complain about her. I should be very grateful that she's even here babysitting him so that I don't have to be the one!
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Book, so wonderful to hear from you and that Dad may be realizing there are some business matters he needs to take care of.

MCWatz, if you think dementia is becoming an issue you need to check on the status of Mom. Does she have all of the necessary documents in place? Powers of Attorney, Do Not Resusicate, Living Will etc? These are very important to have should something happen to mom to become incompetent or some sudden medical event.

Yes, you should go see her. Get her to the doc for complete evaluation and an elder law attorney to help get things in order. If dementia, there are some causes that are treatable, and many that are not and the disease is progressive it will only continue to worsen not get better.

Maybe visit continnum of care communities to find something that she likes. She may be ready to move now, though most are not; they think they can continue to care for themselves when in fact that is not reality. They do not understand that they need help and many remain in denial until the disease progresses to the point that they think they are just fine and there is not a problem. Best wishes as you proceed, this is a very difficult time for all involved.
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Well, FIL was back to his normal today, alert, oriented, awake. Not sure about his walking.. but RN said they gave him a painkiller ( he takes at home) for knee pain last night/this am. So maybe when he said he couldn't walk it was from pain, not an other problem. Still trying to get BIL to bring his dang teeth in so he can eat better! Not sure why he is stalling, but FIL needs them. But he will be there until Monday at least... SIL is getting a much needed break , says MIL is a treat these days except for the incontinence
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After 4 APS investigation for false allegations i have decided to start a movement for us. As a caregiver we are treated w the most disgust over all jobs. We do a job no one else wants. Mostly everyone i know says let him die in a NH. Nope. Not happening. Im fed up w societal attitude from ER dr to family dynamics. We have no one to protect us from all that. If you are interested im just getting started and would love to get the networking started. Jill Howard on Facebook. Please friend me and lets do something about the disrespectful attitudes we live with.
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Jill, I'm going to respectfully disagree with you. My mom is in a nursing home, and she's thriving because of the good care, social acivities and many watchful eyes, including ours. When my mom's dementia makes here think od things, there are many ways to distract her. I'm sure you'll find many takers for your point of view, but there are two sides to this story.
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Dont be nieve to the political movement thats "supposedly" concerned for us caregivers. The newest legislation creates a new agency to put us under more scrutiny. I understand the need to protect the volunerable elders and sick, but where is our advactes? My desire is to see advacy at the table next to us while we look at another APS agent. Lets be fair and give our advacy to hold as much power as APS. My goal is to inform everyone whats really going on. Dont be foolish and believe in happily ever after.
We save the medicare and medicaid over 80 billion dollars a year. I am not paid nor is over 30 million other hard working caregivers. Yes the suicide rate is at 50 percent and climbs more each day. Some families have money to place their loved one in a dementia facility or NH. I don't and either does the majority either. Networking and standing up (when u want to fall over) , I'll be there fighting. Just support is all i ask.
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Where are you Jilly? What is the new legislation?
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My husband had a stroke 3 years ago. It took 2/3rds of his right brain. Hes incontenent, paralyzed, has horribly scary moments of dementia. He has grand mal siezures and has two stints in his heart. He only wants me to care for him. Hes afraid of his family. His sister is a cop in spokane, wa. She has been the natl union rep for years. So she knows exactly how to set me up for murder when he dies.His daughter who lives here is a geriatric RN is taking orders from her. Anyways, between the two of them they have had all their professional buddies call and make false allegations of drugs and abuse. They never find anything but it takes it toll on me and itll never end. See, he gave me POA of health and finances. His dsughter the RN waited all her life to tell him what to do when he got to this condition. Shes mean.

Yes, im angry. Enough to not let it happen to those of us giving our entire existence for those we love.

Its healthy to use anger to help better the world. More people shouldnt be afraid to get angry as long as its used to do good. This is bigger then my issue its a natl issue. Everyday that passes remember the caregiver who decided there was no other way out but suicide. I have experienced loss of two caregiver friends who took their own lives by a gun to the head.

So this may be too much for most of you but mark my word. In 2 years caregivers will have so many agencies crawling into thier private life and you'll see the suicide rate skyrocket. Thats not even talking about thier kids and loved ones and their pain.

Say what you want about me. It really doesnt bother me because what im starting here is the right thing for all of us who hurt so much from exaustion and no end in sight. Caregivers of America wont be mistreated as long as we start making noises.
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There's an AARP policy paper on protecting family caregivers from discrimination. There is some sort of legislation pending in NYC, but i don't know much about it.

I wonder who is making reports to APS in Jilly's situation? If it's family being mean, I'd ship the elder off to them in a heartbeat!

If the elder themselves was reporting abuse, that would be a clear indicator that i needed to leave.
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Thank you. Im almost ready to ship him there. Famoly is just jealous. But still ugly. Thank you so much for support. Have a blessed day.
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Jilly I comend you on your feelings about the need to do something about this. Get yourself to the local college and take some classes on health care administration, etc,, and "go get em".. They will show you ways to articulate and write for policies, get financing, and much more.
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I'm sure ALL of you on here will agree with me. I am sick to death of other people in my life telling me about their wonderful trip to Mexico. The fresh seafood, the beach, how wonderfully warm it was!

I don't like being in this place. These are wonderful people in my life. They mean a lot to me. I just, well, fantasize about doing that myself sometime and know it's not reality. Instead I get to take care of their cat.

I have crazy mom and a kid in college. No money for fun at all. Dining out is even a no go. I know some folks are worse off than I am. My dog has Cushings disease, my brother overseas has syringomyealia (only sib). He is in a really bad place. He was my rock but is falling apart due to his problems. It's hard. Sometimes it just is bad. I've done bad before. Just be with me with encouraging words. I love you AC friends.
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windy, I tell myself that every place in the world is as good as any other if we're alive and can enjoy it. Going to the local pond and watching the herons can be as fun as going to the beach. Hiking on the local trails can be as fun as hiking the Smokies. Nature is rich all over.

Now getting you to feed their cat, then coming back with all the fun stories and pictures is just plain insensitive. I think coming home with a great present to thank you would be so much better. I mean, they would have had to board the cat if you hadn't taken care of him/her. That can be big money.

I am so sorry about your brother and your dog. Wish we could fix things for each other and make them better. I hope a big ((((cyberhug))) helps a little bit.
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Well it finally happened..

Mom asked me what her name is? Who's her father and why did she have a different last name from him.. I told her she married my father and showed her wedding picture.. She said "Oh he's a good looking fella"? Lol.. Yes he was!

I'm sure she'll become more alert later in the day...

Just a first for me!
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A&A, it is sad to these sorts of progressions of this dispicable disease! But, good for you finding the humor in it. Everybody should do the same it make the life of being a caregiver much less stressful! With my Mom, most of the time I would do the same. The most important thing I found was to not try to explain to mom, just go with the flow.

My mom was always shocked when she found out she had remarried. It was not until she was 80, that memory is long gone. The most difficult of this was when she would accuse her hubby of lying about the marriage. And that was very, very hard for him and he is actually sort of insulted that my mom does not use his last name.
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It funny how she doesn't remember being married but knows I'm her daughter!!

Like she would have had sex without being married!
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A&A, strange how that brain works, or doesn't work! The majority of the time mom knew who I was, but many times thought I was her sister.

funny! and it was the sleeping together thing with my Mom, since she didn't think they were married, she knew she certainly should not be sleeping with him. Before their move, I was considering furnishing another bedroom, convert a sitting room or office to a bedroom for those nights when mom would become agitated so she would not have to sleep with him.
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Glad it's just so sad.. Dementia stinks..
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