
Many of us, myself included, come from a dysfunctional family which adds a lot of weight to the challenges of caregiving. I have read stores on various threads on other topics and decided it would be good to have a thread just for this topic for people to share, vent and discuss.
The idea for this thread originated on the thread named "The Caregiver....How are YOU doing today?"
Sharyn, I'd like to give you a "bright" side to your mom calling you all. At least she's calling you at home and not at work. SOMEONE gave my father my work phone number. He hasn't called me in a long time at work. I have Both my cell phone numbers on the board. Nowhere can I see my work phone. Now, he calls me at work for the simplest things that can wait until I come home. I was so pissed off at both of them. Unfortunately, sis fled when my mouth started. Too bad, because I think she gave him my work number. I did tell father that if he continues to call me at work, I will go next door to brother and tell him that I'm leaving and he can take over father (as originally planned - I care for mom, bro care for father). That just pissed off father because he has verbally disowned bro-of-next-door.
Your mom made these changes for a reason. It will be quite the shock to other family members, I'm sure. Best wishes with all of it!
https://www.agingcare.com/articles/estate-administration-probate-after-death-in-family-153107.htm
I am still waiting to get a certified copy of the death certificate because the doctor has not signed off on it yet. How frustrating! I need to start probating the will for it only gives me 60 days to remove what the will says I've inherited from the house, out of the house. Also, there are some joint ownership accounts and investments which need dealing with that were owned by my mother and I with right of survivorship. This will probably anger my step-brother and step-father, but that is how she set things up.
Google: Carrie prank at coffee house.
By the way, Sharon, my aunties had set up an ancestry link for us. I forgot my password. But, it's linked to our email. When someone adds a photo or anything on our ancestry tree, it would send us an email that so-and-so added ....comments or photos. Then I can log in and read what it.
If you're interested in this family tree program, it's called: Genie.
I would take them to a shop, have them scanned and put on a dvd. My aunt did that with many old, old, photos, added music, etc. This would be wonderful Christmas gift for many in your family, shopping done!
My uncle also had Alz...his wife died in their home and he was living in the house for 2 days before a neighbor discovered his wife had died. The state of PA contacted my mother here in CA as she was the only living relative who could make decisions (this was in 1998). Please get your family members to get DPOA written up...it is so important. Anyway my mom worked with the state of PA authorities to place my uncle in a facility and they kept my mom informed of his condition and followed her wishes for his care. My mom was taking care of my dad at this time who also had Alz.
What can I do with these photos??
Sorry your friend is Texas is never available. I have high school friends that live within a mile of here. I run into them when in the grocery store, etc sometimes. They always say they will drop by when out for a walk. This is one of the consequences that I must pay as a caregiver. My situation is uncomfortable for them as well as my mom's condition. One day, this too shall pass.
I am so focused on the health of my hubby, eating better, reducing sodium and carbs that I put my mom on the back burner. She has called me twice today. Not a problem because our conversations were pleasant. She has been at the community now almost 6 months. She still wants to go home which I expect that as long as she has a memory of her house. She called me early this morning, she was upset and close to tears. This is what is hard for me, when she cries, ,because she does not do that often. I am the emotional softy who cries easily, LOL!! She was sad because she said she had $10 and someone took it. She couldn't find it anywhere. If anyone took it, it would have been another resident because the staff has been great about not taking things. I know this because when we first moved mom in, my sister did not go through my mom's dresser drawers. After 3 weeks, I went through everything looking for keys we needed and I found a small jeweler box she had with a diamond wedding set and other jewelry. She had over a $100 in her wallet for a long time until I could get her to agree to let me put it in her accounts. Anyway, I told her this morning I would come over tomorrow with Midget and we would get this taken care of. She accepted that. She called again this afternoon, her concern is the blurriness in her vision. We talked about the surgery the eye suggested, she is against it and so am I. I really think her vision is Alzheimer's related because the eye dr. said she has had these little bumps on her eye for a long time. Getting her to wear an eye patch for week will be impossible, not rubbing her eye due to discomfort...she wont understand to not take off the eye patch. Maybe i will check out that prescription for moisture drops in the eyes and see if it may be a better alternative to using OTC moisture drops. Alzheimer''s messes with the brain so much as it progresses, since we have taken her to the eye dr. in last 3 weeks, I really do think this is part of the disease messing with her vision.
I tried calling my old friend in Texas, but she didn't answer for whatever the reason. I will not call again...the ball is in her court now. No big deal as too many years have gone by since we have talked and our lives have taken different directions. I didn't expect her to call me last night when she asked if she could call. Anyway, if it is meant for us to make contact by phone, it will happen. Have a good day everyone!!!
Many here understand your dilemma as they have been abused since childhood. My mother does not have Alz but has had Borderline personality Disorder and narcissism all her life. Now she has been diagnosed with paranoia, and is barely competent. I believe this is due to aging. I have found that I do best by being honest with mother and by setting boundaries which is what I have learned over the years I have to do for my own protection. I wasn't sure how to deal with the paranoia, but finally ended up gently but firmly telling her the truth. It is what works for me at present. . If my parent was in the last stages of Alz, I don't think it would work.
However one constant is that no one has to take abuse. I wouldn't scream or let your frustration build to that degree. I have told mother that if she is nasty to me, I will not visit her. Mother also finds fault with everything around her. I may listen for a short while, then change the subject or tell her I think they are doing the best they can and over all she is well cared for. If she gets mad at me I leave, or cut off communication for a while. Even if your mother is in early stages of Alz she will recognise boundaries I believe. In any case, you do not have to stay in her presence and listen to things that upset you. Many times I (and others) do not answer phone calls, or emails, and/or remove ourselves from their presence to preserve our own sanity.
Dysfunctional parents use FOG fear obligation and guilt to manipulate others. Practice recognising these and not reacting to them. Detach from her and set boundaries.
some ideas about detaching -
Accept that they are responsible for their own choices
Anger –deal with it in a healthy way
Blame –don’t blame and don’t accept blame
Consequences – face them and see that others experience them
Decide what you are willing to do and what you are not willing to do
Detachment is not a feeling so much as a choice of behaviours, though the feelings should follow the behaviours. Detachment means you can maintain positive behaviours towards to others –kindness, compassion,
Don’t take on blame, guilt, manipulation, anger - don’t enable
Focus on yourself
Forgive, but don’t forget the need to protect yourself
Grieve the relationship as it was, the hopes that you had, the mistreatment you received,
Refuse to be manipulated e.g, emotional blackmail
Respond, don’t react
Separate - physically, emotionally, spiritually, mentally, socially from others behaviours/feelings
Set boundaries
Say “No”
Space –create it between you and them
Try not to take the behaviours personally
Treat others and yourself with love and dignity
You can only control /change yourself – your emotions, your behaviours –do not take responsibility for the others feelings or behaviours
Realise it is a process and that you will make mistakes and get “sucked” in, but that you can learn from your mistakes.
As the disease progresses you may need to change your tactics.
(((((Hugs)))))) let us know how it works out
Even though I've had to handle transferring assets, rehabbing her house, her diagnosis and placement, I've been pleased that I've done a good job. So, what's the problem?
Mom verbally and abused me from the moment I was born. I've had emotional/mental illnesses and in treatment for 35 years. I am handling my life well and dealing with people in a positive way. I've dealt with mom's abusive behavior and learned ways to cope....which has include limited time with her.
It is hard for me to separate her dementia symptoms from the way I was treated all my life. Yes, they are worse and happening to others as well, but mostly my brother and I get the rage lambasted on us. As I read posts about how to deal with repeating stories, for example, I want to scream! I won't continue to listen to how I have done...blah blah blah..and am a liar and deceiver and a member of the selfish generation...etc. I am frustrated with her constant putdown of anything that goes on at the Residential home. Everything is a twist of the truth, negative, and paranoid. So, this is dementia? But, this was my life as a child. Did she have dementia then? Do I treat her the same as I've learned in the last 35 years or do I need to adapt because it's now medical? Granted, she has only been diagnosed and placed for about 2 months. but I have so many questions that are rolling around in my head. Unfortunately, I can't find a support group in my area. I need help so that I don't slip back into an overwhelmed stupor!
Joan-i am glad you are feeling better. The flu already...I hope the flu season is not too bad. I had a bad flu once, with pneumonia...not fun at all.
Our aspens are scattered over the sierras, some are hard to get to due to the terrain.
We didn't miss having mashed potatoes and the small amount of stuffing I put in the breast cavity was perfect for the 3 of us without being too much extra on the carbs. The veggies I made, hubby and my son both thought it was rice,lol! I grated up green and yellow zucchini, carrots bell pepper and onions and added sun dried tomatoes with garlic and baked it at 450. They both ate it up thinking it was rice.
Ballnchain-welcome to the thread! You are wise to back away and just visit your mother at your leisure enjoying the time together. My sister started to get a little forceful with our mom when mom was diagnosed as incapacitated due to Alzheimer's. She found out mom may be mentally incapacitated but she can still put up a good fight if you try to force her to do something. Sis and I work togetheras dopa, she being the primary, me secondary. Sis lives out of town so I take mom to most of her appiontments. Mom is in memory care now as sis and I both have to work. Sis has health issues too and she takes care of all the financial which I am glad. I think I have the easier job of taking care of the medical.