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I hate this disease, dementia. Hate it, hate it, hate it. Mom called me this morning and we spoke briefly on Facetime. She asked, once again, when my brother and I would deliver the lounge bed she ordered. I have no idea what she is talking about. I try to console myself with the knowledge that she is safe where she is, in assisted living, and fairly comfortable. But I find myself grieving just about every day.

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Of course you're grieving, and all of us that have been through or are still going through caring for someone with dementia HATE IT!!!
When mom asks where her lounge bed is just tell her that it's on backorder and you will let her know when it comes in. Eventually she'll be on to something else.
You must learn little "fiblets" to keep her and you calm.
I'm glad to hear that at least your mom is in assisted living so that the brunt of her care is not on you. That is a blessing for sure.
You're going to be ok, as this too shall pass.
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Reply to funkygrandma59
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We all hate this disease. Dementia sucks the life and soul out of the person that has it, the family and friends.
She is safe that is the important thing.
funkygrandma59 is right on with the "fiblets"
Back order
Can't be delivered until next week
They ordered the wrong color
And here is an idea...
If she is wanting to replace a couch or chair in her room get a cover for it. When she is at lunch or at an activity cover what she has with the new cover and she may think that she has a new piece of furniture.
Rejoice in the fact that she can still call you and talk to you. My Husband was nonverbal the last 7 or so years of his life so if he said even 1 word I would have been happy.
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Reply to Grandma1954
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When I'm feeling upset or unsettled I make myself do something productive. Since you don't have your profile filled out, I will suggest that you make sure your Mom's legal ducks are in a row: that she has a PoA assigned (before she gets too far gone cognitively), an Advance Healthcare Directive, Will, etc. I'm hoping she already has this in place.

If you are her PoA and, if you haven't already done this, read it to see what is required to activate the authority. Usually it's 1 official medical diagnosis of cognitive/memory impairment. Make sure you get this done so you don't have to do it in a crisis.

A certified elder law attorney will determine, during an appointment with her, whether she has legal capacity or not. The bar is low so don't presume she doesn't meet it.

Everything about dementia is hard. I wish you peace in your heart on this journey.
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Reply to Geaton777
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So sorry wheat, I completely understand, mom doesn't have server dementia, but I took her out yesterday to are local Apple orchard and then are local dairy store. As I was doing it I was thinking and remembering last year and how much easier it was, and how her health is failing, and there may very well not be a next year.

Every thing I do with her now, I'm thinking this may be are last time.

It's hard and it stinks, but it's life.
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Anxietynacy Sep 14, 2024
I will also add, that I'm learning better how to compartmentalize these issues better, in a more mentally healthy way.

By accepting, this is what happens, we are not alone, let myself be sad when I am, but also how to put it out of my mind and enjoy my life.

Because all of are life's are short, every day we have is one less day. And I try not to ruin that day I have , by worrying about something that I have no power over.
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Besides guilt, and besides grief, there’s another G word, and it’s gratitude. Gratitude that she is, after all, in a place that keeps her warm and safe. Gratitude that there are funds to pay for it. Gratitude that there is now a whole team to care for her. It’s the best that anyone could do.
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Reply to PeggySue2020
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Looking at your post I thought "There's just no answer to this grief".
Then I looked at your answers below, and found them so beautiful.
Wheat, take care.
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Reply to AlvaDeer
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Dementia is HORRIBLE. I’ve been dealing w/my mom’s for 8 years. She’s now lingering in moderate/severe ( leaning more severe ) for a long time.

I’ve found the phrase, “ Everything is pre-arranged” to be very very helpful. “ No worries, the payment for lunch is pre-arranged”, “ The schedule for the family roller skating party is pre-arranged”, “ The lounge bed logistics are pre-arranged, it’s just a slow process…” etc…that kind of thing. May have to repeat the phrase but it often works for me.

Best to you…
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Reply to Madisoncuckoo7
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I think we all grieve(d) the loss of our loved one with dementia long before they actually pass, which is why it's called "the long goodbye". To watch a person lose more and more of their mind every day is even worse than watching them lose their strength and coordination. Although watching my father die from a brain tumor was dreadful also, I must say. The death process in old age is what takes a terrible toll on us "children" because we've always seen our parents as strong, invincible creatures there to protect US. Now that the roles are reversed, it's a sad and grief inducing situation.

My mother died at 95 from advanced dementia and CHF after 6 years of a progressive downhill slide with the dementia. I cried every time i saw her for a visit in Memory Care Assisted Living. I didnt try to stop the tears either, I just let them flow. Same with my father who was devastated by the brain tumor which rendered him immobile at the end. It tugged at my heart to watch them fall apart, knowing there was nothing I could do to fix the situation this time. Only God could intervene and end their suffering at that point.

I'm sorry for your pain. It's the price of love, Wheat. May you find peace along the way for yourself.
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Reply to lealonnie1
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I suggest you look at this from a more positive view. I have been dealing with my dementia husband for 9 years. He is at home. I don’t want to do it anymore, put it makes me sadder considering putting him in a home. Be glad you have some help with taking care of your mom, and that you do not have to do it alone.
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Reply to Atlasshrugged
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I understand how you feel. I felt like I lost my Dad a thousand times before he actually died. One thing I can tell you is it makes the actual final loss a little easier, since you’ve already grieved so much. There is some relief (and then guilt over the relief). Here are my suggestions: (1) Tell your mother you love her every time you say goodbye. (2) Find a couple things you love to do, that lift your spirits, and do them after you speak with her (mine was listening to a particular type of music). (3) Embrace this time you have her, even though she is compromised. She isn’t gone yet, just different. (4) Make her a photo album or scrap book of things she likes (be prepared for it to be destroyed or lost). (5) Send or bring her her favorite food. (6) Basically treat her the same way you did before, even if she doesn’t respond the way she used to. I was convinced my Dad understood most, if not all, of what he heard. He just couldn’t reply or remember.
Now that my Dad is gone, as hard as it was, I’d do anything to have him back.
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Reply to AliAliCatCatCat
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Wheat, I'm so sorry you are going through this. This disease is a marathon not a sprint. Continue to do self care for yourself, whatever that looks like. Your Mom has great sons.
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Reply to brandee
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Remember that you are making the right decision for your mom's care. I too have been grieving for my mom who is in a facility. We are not given a set of instructions for what's to come later on in life. These dementia challenges take us through a whole range of emotions, but you must take care of your mental and physical health too. The emotions will cause your blood pressure to go up. We want to remember the good memories. Your pain will eventually subside. Try to do things that you enjoy. Have a purpose. Life is so short, so make the most of it!
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Reply to Onlychild2024
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Anticipatory Grief - it's real thing.

Back in early 2020 it would hit me. I would almost be sick to my stomach with grief over my Mother, and here she is still chugging along at 97.

Anyway, what you're feeling is a normal part of watching your Mother go through that slow decline called dementia.

I wish you peace.
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Reply to southiebella
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Though your mom is still with you physically, this quote I read recently on James Clear’s newsletter came to mind when I read your post.

Writer Heidi Priebe on love and grief: 

"As long as there is love, there will be grief. The grief of time passing, of life moving on half-finished, of empty spaces that were once bursting with the laughter and energy of people we loved. 
As long as there is love there will be grief because grief is love's natural continuation. It shows up in the aisles of stores we once frequented, in the half-finished bottle of wine we pour out, in the whiff of cologne we get two years after they've been gone.
Grief is a giant neon sign, protruding through everything, pointing everywhere, broadcasting loudly, "Love was here." In the finer print, quietly, "Love still is."

https://jamesclear.com/3-2-1/September-19-2024
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Reply to 97yroldmom
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Wheat85: Prayers sent.
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Reply to Llamalover47
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Perspective is a choice. You can grieve what you see has been lost when you think or talk to your mom. OR, you can be thankful for the health and safety she currently enjoys. Usually, you should be able to redirect the conversation to something that causes you/her less distress.
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Reply to Taarna
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“Grief is just love.
It is all the love you want to give and cannot.
All that unspent love gathers up in the corners of your eyes, the lump in you throat and in that hollow part of your chest.
Grief is just love with no place to go”
Unknown.
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Reply to Evamar
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Dementia is a thief for sure. It robs us of mutual memories and meaningful conversations. I hate it too. But - you still have her to visit and talk to in dementia-speak - which is its own language. Be grateful for that and take care of yourself.
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Reply to jemfleming
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There's an advert for the Alzheimer's Society currently showing on UK TV. The actors speak about the "first time that Mum died" when shd forgot how to make her famous Sunday roast, then the next time and the time after that, mentioning when Mum couldn't remember names and other stages when we lose our loved ones as they lose themselves a little bit at a time.

Because we lose our loved ones with dementia, piece by piece, their death seems drawn out over years, even decades. By the time they die, we have been anticipating their final leaving for so long that it's difficult to grieve properly. At least that's how I'm feeling right now, as I prepare for Mum's funeral this coming week.

I've just been picking out photographs to share at the wake. I wish I'd done this before, to keep Mum, when she was herself, in mind.
So, that's my advice. Create a memory book. Not for your mum, but for you. It will be tough, emotionally, but it will help you remember your mum as she was and to tell yourself that this version of your mum is ill. It's her damaged brain that is asking about a sofa, that makes your mum fixate on things, prevents her thinking about others and being respectful of their time and energy.

I stopped creating a memory book for Mum when I realised that memories could be painful for her, especially when she realised that she was forgetting. But I wish I'd carried on creating it for me.
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Reply to MiaMoor
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One way I coped when Mum was alive was by reminding myself that I was doing what I could to make Mum comfortable.

I wouldn't sacrifice my own life for my mum's, and I realised that we cannot make our loved ones happy, but she was safe and had what she needed, if not always what she wanted.

I reminded myself that I was always making decisions in Mum's best interests, but that I was not superhuman. My best had to be good enough.
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TouchMatters Sep 23, 2024
Thank you. So very helpful and supportive. Gena
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I used to drive my father, who lived with me, to see my mother in memory care. He had cared for her for years. On the way home once he said 'you know your mother's gone, don't you'. Had to agree.
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Reply to Sharon44
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It is one of the most cruel conditions - for a family member, and I can't imagine what it must feel like to you, your mom's son.

You are grieving in slow motion. Part of her is here and part of her isn't.
This is heartbreaking. And, my heart goes out to you going through this.

I'd say that the is no such thing as "should" - although I believe you mean to say 'how do I do this? go through this awful pain? heartache?

As is said 'the only way out is through.' Meaning you intentionally feel as deeply as you can; do not try to avoid how you feel, get it out anyway you can. Scream, cry, go for walks, talk to a friend/church support.

Allow yourself to be as you need to be.
There is no 'right' way to grieve and especially when your mom is still here physically.

As you indicate you are burned-out, get help as you can to support you to either do some of the work / needs you take on or do whatever you need to support you.

Figure out what you are doing that you might be able to scale down or change, i.e., if you visit your mom 5 days a week, find volunteers to visit her 2 days a week - giving you time to go for a walk, to a movie, a museum - even take a hot bath or get a massage. Take some time for you.

Expect to grief and expect to not know how that process will unfold.
We never know. The process is different for everyone.
Do not judge yourself or your thoughts or behavior if somewhat erratic.
When my mom died:
- I put a pot of broccoli / vegetables in the cabinet instead of the refrigerator - and found is 2-3 weeks later.
- I missed a turn on to the freeway THREE times.
- God knows what else I did.

Get into therapy / grief counseling. If you do not know how to find a therapist or grief counselor, ask local dementia organization for referrals or the social worker where your mom resides.
- Get professional support.
- Friends are helpful although many people are very uncomfortable talking about death / dying / or even dementia, esp if they haven't personally experienced it (with their own family / friend) and find it hard to relate to you. The 'best' friend is one who gives you all the room you need to talk, be quiet - LISTENING --- and just be there with you - not offering advice or suggestions (unless you ask). Most people want to give advice (well meaning). A trained therapist will give you the space to feel and express however you feel.

Grieving is a slow process.
It can't be rushed. It has a psyche mind / energy of its own. It can feel very bizarre from my experience. I was totally thrown off balance emotionally, mentally, and psychologically. I couldn't 'will' or 'push' myself to feel differently. I had to be with how I felt, without trying to numb it out or be in a better mental place than I was. I wanted it to BE OVER ...

This is a good place to come to talk and let us know how you are doing.
Many of us have been in your shoes and can empathize.
We will listen.
You have friends here who understand.

Gena / Touch Matters
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Reply to TouchMatters
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My dad has dementia too from alcohol and he became an alcoholic because he got sick from sedeth and couldn't stand the pain. My mom joined him on the whiskey train. I brought them both into my home to try to help them after they destroyed everything they worked for because you can't force them to do anything. My dad calls me everyday asking when I am coming to get him and I can't because my mom has become violent towards everyone. I know he is safer there and getting what he needs but I still cry everyday. It never gets easier and putting out emotions aside to try to help them and do what is best for them is not always easy. I just joined this and saw your post and I just want you to know your not alone I think there is a lot of us struggling trying to help our family. Hang in there, your doing great.
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Reply to Christine1980
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So sorry for your grief and struggles. My 95 YO dad has dementia and is living with me until we can get him into the VA home. The process is taking way too long and I can’t wait to get him where I know he will be better cared for, more stimulation and conversation than I can provide working full time and trying to keep him well fed and safe. So be content with the fact the your LO is in a safe environment. I have such a difficult time conversing with him because he brings up topics that are difficult to discuss. He was a home builder for years and still wants to renovate. I need to get better at the fibbing. Sadly he no longer recognizes my home (that he built). All of this is SO hard. I know I will experience the same feelings as you when we drop our dad off, and unfortunately we won’t be able to visit him often (1400 miles away), but it is our only option. I will worry that he won’t get “daughter” care anymore. I commend you on your heart and how much you care, and wish you peace throughout this journey.
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