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Where are you Jilly? What is the new legislation?
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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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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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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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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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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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{{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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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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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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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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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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Thank you both!
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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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Ahhh, Pam, when it rains it pours! Best wishes for everybody, they are fortunate to have you!
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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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Hi Glad! Almost time for bed for a working woman?
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Another completely kind of fowl?
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Send that is a completely different kind of foul!
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Tatianna, do come back. You have found a safe place to vent and get encouragement and my do you need both. When I read your posts what I hear is a person who needs a safe place to unload and needs support. You can find that here.
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Gershun, You aren't gonna shoot my fowl, with your kitty, are you?
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Wow, could we lighten up a bit, give her some space?
Stacey, I especially enjoyed your corrections all over the site for limiting fowl language, while swearing! That was truly awesome! No, I am serious! Maybe you are channeling captain? lol. I was doing that once after he offended everyone, then, not my job cause many liked it. (The fowl, I mean) Thinking this is a phenomenon I don't quite understand yet. Forgive me.
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Tatianna, don't worry, I don't think you've affected anyone at all! It was my simple recommendation that you withhold especially the F word, that is all! We all need a place to vent and to ask for guidance and support, and you are just as deserving as the next! Do come back for help! I admire the fact that you found your way around this blog, as it was a great way to introduce yourself! There are a lot of very wise people here on the AC, ready to give you great advice, day and night, and there is a difference in the day and night crew also, to give you more prospective on your questions! We all have a lot to learn from one another! Good luck Sweetie!
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I just swore again in my post. I apologize again. I won't really be posting much from now on anyway.
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Sorry about my excessive profanity. I really and truly did not mean to offend anyone.

This transition has been rough to say the least yogagirl. I feel like I lost a part of myself when I left NY. Whatever the h*ll that means. I'm gonna stay low key from now on. I highjacked enough threads and annoyed enough people. Is there a way to delete posts on here? I tend to rant and complain a lot when I have a lot on my mind. I should just write more in my journal instead.
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Yoga, my mother has been here two years and told me yesterday she still feels like a visitor because it's not "her home"..
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Tatianna, I have been following your posts and all the great responses.
I'm real tired from taking care of both parents and my sister just had an operation. That is why I haven't been posting much. Sis and I had an interesting conversation today.
She told me years ago, homesickness was considered a real sickness. That is how painful and challenging it is to move.
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Good advice staceyb!!!!!!
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Tatianna, it's one foot in front of the other, that's all any of us can do. Start writing lists, and checking off boxes. Lists to help your Mom, Lists for ideas of what you might like to do in the future, and then start making the steps to completing each task. Don't be discouraged from some of the responses you receive here. These people don't know you, and you are anonymous to them. Keep coming back, and soon you will feel more comfortable writing down your concerns and comments. Also, sweetie, try to refrain from swearing, as you don't want to make people angry. Not me, but others! You are younger then many of the posters here, and I get the lingo, but it really isn't nessasary is it? Develop a thick skin, as some posters can be quite cutting! It is their way to help, but still! Have you ever had counseling? That might be a good first step too! I hope you are having a good day!
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