Mom is 85 years old, she was in the hospital for 11 days, I rescued her and brought her with me. She is getting better, but my blood pressure has gone up, my life has been given fullen to this woman. She feels I owe her for years ago, I am constantly getting her back to health, I am tired. I can't do it anymore.
I have been to nursing homes and I know about their abuse, I want my mom to be treated better than that. I know that care giving is tough, but I also know that you cannot make anyone feel guilty unless you allow them to make you feel guilty.
Think about why are caring for the person you love and hold fast to that. Care giving is tough and no easy task. But do not let anyone make you feel guilty about why you do it and being a care giver.
I take a lot of crap from family and have, sorry to say I am just a Bitch to them now and tell them to mind their own business. In fact, I have little contact with them because it is not healthy for me and it is not healthy for my mom. I try to make sure the environment is healthy for both of us.
So remember why you are caring for your loved one and remember there will be days that we feel extremely low. I have my share of bad days, but I have conversations with myself, pray and talk with people here. This is a great group of people that are happy to share their stories.
When my health started deteriorating I realized it does no good to hold on to the "guilt trip". If my health fails I can't take care of her. We've had to have some serious conversations about the way she interacts with me. I had to stop doing too many things, and give some things back to her as her responsibility. She needed that for her own independence as much as I needed to stop doing it. The more I did, believing she needed my help, the more she pushed back on me. Some things were hard to let go of, because she wasn't making right decisions. But the truth is she is still her own person and she still has the freedom to make her own choices, however good or bad they are.
Everyone is in a different place and I don't know the specifics of your situation; however, I do know what it's like to take on too much responsibility. Then when I try to force something there's conflict and I suffer for it.
We talk and I let her know what I will help her with and what I can no longer help her with. Then she seems to accept more responsibility (where she can) and take steps (for example) to help her remember to do things. (Bear in mind, she is still able to understand these conversations; I do not know what your loved mom’s level of cognition is right now.)
If you have time, there is a book called Boundaries by Henry Cloud and John Townsend. It’s an easy read. You may want to skip past the first chapter for the sake of time; however, you may also identify with some of the things in the first chapter. Your choice.
I know that the temptation is to put her health before yours, but remember if your health fails, you cannot help her. When your boat is sinking, you put your life jacket on first and then help the victim. (I can’t think of a better example right now, but you get the point.) And no guilt trips. You are doing this because you love her, not because you owe her.
I have a question for JessieBelle: You mentioned that Texas is a great place for senior services. I recently moved from Austin back to Wisconsin. Dad passed away in November and I would like to move back to Texas, but Wisconsin has a lot of services and aid for seniors and I'm concerned that she/we will not get the help we need in Texas. When I called the Department of Aging the representative told me we would need to move there first to find out what she would be able to receive. Can you tell me what kind of services you receive for your mother/father? Can you give me some examples?
You can start a new conversation if you would like.
realized that even though I know my mother better than anyone else, it still
doesn't make me an expert with Dementia or Alzheimer's. That's the bottom
line. You have valid reasons for keeping your dad where he is right now.
He needs the help of experts. It doesn't mean you love him any less.
It's just this time of life for him. You have every reason to be concerned with the nights and his walking around, his size, his instability, and more. Yes, of course you could keep him at home with you, but he probably won't be any happier. That will only put more stress on you, in addition to wearing you down. When my
dad was about to be released from rehab, due to a stoke and congestive
heart failure, the doctor told me he should NOT return home, as it will be more
difficult to get him back in a facility, where he needed to be. I took their advice
and was glad I did. I had to put both my parents in a facility, at the same time. And though dad passed away 3 months later, I really lost both parents because
of my mom's disease to Alzheimer's. Dad called me everyday, telling me
I had to get them out of there, NOW! I knew that wasn't an option, but regardless, I did feel pretty bad.
Since dads passing, the one thing I do regret is keeping my mom in a private room. I've come to learn that with Alzheimer's, sometimes it's best for the patient to have people around them. At the time, I felt I was in her best interest for her to live alone, when in fact, it was the worst thing for her. She lived in fear, she hallucinated, she didn't recognized her surroundings and she ultimately walked out of the facility, trying to find her way home. Thereafter, she had to be placed in a locked down facility. Now THAT I couldn't do! I found one of those residential homes with 6 other adults at her level of illness, 5 minute from my home. She's still scared, still cries, still hallucinates and is now going into the PPA phase of her illness (Primary Progressive Aphasia). This is where they can no longer form sentences that make any sense. They also lose their ability to write. Over all, she's well cared for and I can bring her home on a Sat or Sun.
So Butterflygrl, I'd go with my gut feelings, but if you're dad is already in a NH, and needs to be there, I think it could be a big mistake taking him back out, and THEN having to do it all again. This of course, is how I had to deal with my situation. My dad was very ill and my mom Alzheimer's had progressed quite far.
Well I hope I was of some help to you. Ultimately, you're the one who knows how bad off your dad really is. It's never an easy decision. Good luck.
I am truly sorry that you are going through a difficult time in your life. I can relate to your frustrating moments. I have been taking care of my mom for almost seven years without hardly any help from my siblings. I have a lot of health issues myself, which makes it more complicated sometimes, but I do not let my 90 year old mom see me cry or look bewildered. Have you looked into getting assistance from a home health agency that is covered by Medicare to help with her grooming, bathing, cleaning her room, etc.? That will take some of the load off of you. I know that it is hard, but ask God to give you strength to carry on; do the best that you can and your Blessings with follow. I sincerely wish you and your mom well. Take care.
I realize that care giving is a challenge, but I miss talking with my mom and while I can now it is not a meaningful conversation. So I miss her and she is alive, my siblings do not get what is going on yet and that sadness me.
My husband lost his mother to vascular dementia and he made the choice to see her twice a week after his dad put her in a nursing home. My husband now has a lot of guilt over not spending more time with his mother.
So one has to ask themselves do you want to handle the situation now or have guilt later on. My husband's mother has been gone for about 5 or 6 years now and his guilt is no less today than it was then. I am going to have some siblings that have some guilt when mom is truly gone, I have tried to talk with them and they do not want to hear.
Some of my days are a real challenge and I feel very overwhelmed, but I know that I am doing the right thing. I also know that the feelings will pass, I have this group to talk with and my friends. I have a couple of friends that have been caregivers and have now lost their parents, so I talk with them frequently.
My husband and I now use the expression that it is a new normal when my mom's behavior changes. It is not easy to watch, but the woman that was really my mother is gone and what she is now is more childlike behavior and more of the child I did not have.
So when one gets overwhelmed and tired, I just try to remember why I do what I do and why I care for my mom. It is not a task for the faint of heart, but I know that I am doing what is right. This is how I move on when the days get tough and I know that when she is gone that I will have done my best. I will let my siblings deal with their guilt because of their choices.
Good luck, and take care of yourself - you are giving so much of yourself. You deserve some R&R!