The Cavalry Is Not Coming

Posted by bill2001 @bill2001, May 1, 2023

May 1, 2023 will mark seven years and seven months since my wife’s dementia became obvious, and that I knew for certain that this journey would begin. I had sensed something was “a bit off” before then, but that date stands out as the moment that I knew with certainty. I use the date Oct. 1, 2015 as the beginning of this journey.
I write this today with a light heart, and a feeling of optimism that I have not felt for years. Nothing has changed – my wife is still in the throes of dementia, and I am certainly still an exhausted, burned-out caregiver and fulltime employee. I have not placed my wife in a facility – she is still at home with me, or at the adult day care while I work. As I said, nothing has really changed, save for the continuous downhill progression of this god-awful disease.

Rather than post another hopeless, angry rant filled with strife, I want to share with you how one of my greatest fears has come to pass, and how it is actually a relief. My fear has always been the following:

The Cavalry Is Not Coming.

I have spent many a day frozen in fear of being alone: Afraid of being left emotionally alone, physically alone, and spiritually alone. Alone in feeling my way around in the dark, trying to navigate dementia caregiving as best as I can. Many of us on this board post virtual cries for help. I have gone into this ordeal kicking and screaming, which is a perfectly human and natural reaction to a trauma of this magnitude.

Some measure of peace and calm is found in simply discovering that the Cavalry Is Not Coming.

Family and friends mean well, the medical community cannot do much for a terminal illness, and non-profit organizations do what they can to educate us and mitigate the damage. There is not much anyone can do to help us. We are on our own.

In more than seven years, I can only site one time that I had true, respite level help without a pricey invoice arriving afterword. Once, in over seven years.

In times past, I would have been bitter and angry about this, but I have finally arrived at an important conclusion. I am on my own, and no one is really going to help me. I am no longer bitter about this, as I have finally realized that other people have their own crosses to bear. Odd as it sounds, there is a peace to be had in such a revelation.
In the movie Castaway, Tom Hanks’ character was marooned on an island. At first, he tried to find help: Screaming to see if anyone else was there, spelling HELP on the beach. All to no avail. At some point, he accepted that fact that he would have to fend for himself and got busy with the tasks of survival. He even learned to thrive.

I have taken on the point of view that “The Cavalry Is Not Coming” to epic levels. My wife’s well-being today, as well as my future life, is completely in my hands now. I am now the King of the Castle, Lord of the Manor, Large and In Charge. Yes, I still have meals to cook, dishes to wash, showers to give, medications to manage, diapers to change, and a fulltime job to boot. Life is busy, difficult, and exhausting. But I have some measure of control, and I can call all the shots. That ugly picture on the wall? Gone. Pizza night again? You bet. Two hundred cookbooks on the shelf? We only need twenty. This house needs to accommodate my needs so that I can best take care of my dear wife in these final times. That means removing tripping hazards, redecorating in a light and happy way, and decluttering to the max.

There is a feeling of relief when you just let go and realize that no one is going to help you. The kids (if you have them) are busy building a life of their own, and friends and family have their own problems to manage. I have lowered my expectations to nearly zero, and it has been very liberating. If you have reached this stage (or passed it), you understand. If you are still frozen, kicking and screaming for help, hang in there. Look around you and remember, The Cavalry Is Not Coming.

That said, continue to utilize services that are available. Keep up those doctor appointments, call the Alzheimer’s hotline (800-272-3900) when you are overwhelmed, grab takeout, call friends and family to talk, or even ask a small favor. Use devices and technology to help you – cameras, cabinet locks, grab bars, the “good” diapers, etc. Make everything as safe and foolproof as possible. Be sure your loved one cannot lock themselves in the bathroom, or that you cannot get locked out of the house. Secure anything hazardous. You are the Safety Inspector now. But do not expect anyone to be there to help you change your loved one’s diaper, make dinner, or wash dishes. Get that mindset that you are on your own and take control of it all. Your loved one can no longer help and can no longer make decisions.

After reading this, take a deep breath, and say “I am on my own, and I am doing the best that I can.” I really hope this makes you feel better. This is a horrible situation to be in, and sometimes realizing that you are on your own is just what you need to hear.

This also means that the decision to place your dear loved one in memory care is yours and yours alone. No one can tell you where you are on this journey, and no one can tell you how exhausted you are. You are on your own, no one is going to help you, The Cavalry Is Not Coming.

With Love,
Bill2001

Interested in more discussions like this? Go to the Caregivers: Dementia Support Group.

I just re-read this for the ? Time, and again, this may be the best post I have read on the subject, Bill.
Thank you for this.

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Thanks for putting it so well. It is a slow realization of what it occurring. I think I finally realized that. When we started this journey I thought we can still do things as before but I became aware it’s not just forgetting who we are or where we are but basic things of not being able to dress or use a fork or knife or know the words stove, sink or table. Thanks again.

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Thanks for this wonderful post. My caregiver will face this down the road, I'm sure. You might look at my post on an MCI (Mild Cognitive Impairment) Comment feed--I already have forgotten the exact name. My caregiver and I have just signed up with a virtual company that does zoom care and advice. It is free if you have Medicare A&B (not Medicare Advantage). My heart goes with you.

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Amen! Thank you Bill for your heartfelt message. Unmet expectations lead to resentment so I too have kept them at zero. Honestly, I can understand why people do not want to volunteer to help. Someone once said to me, that our homes have become the ones no one wants to come to anymore. The smells, visual decline, and facing mortality are just a few reasons why.
You mention you are "Afraid of being left emotionally alone, physically alone, and spiritually alone. " As horrible as this disease and the daily tasks can be, there is some routine and normalcy. I worry about being physically, spiritually, and emotionally alone when my husband passes after 47 years of marriage. Everyone says I will be fine but that feels like patronizing. Thank you so much for sharing and letting us know we are not alone on this journey.

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@ksa230

Amen! Thank you Bill for your heartfelt message. Unmet expectations lead to resentment so I too have kept them at zero. Honestly, I can understand why people do not want to volunteer to help. Someone once said to me, that our homes have become the ones no one wants to come to anymore. The smells, visual decline, and facing mortality are just a few reasons why.
You mention you are "Afraid of being left emotionally alone, physically alone, and spiritually alone. " As horrible as this disease and the daily tasks can be, there is some routine and normalcy. I worry about being physically, spiritually, and emotionally alone when my husband passes after 47 years of marriage. Everyone says I will be fine but that feels like patronizing. Thank you so much for sharing and letting us know we are not alone on this journey.

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Welcome to Mayo Clinic Connect @ksa230 ! I think you will really like this discussion; everyone is very open with their situations. And, may I ask, are you the caregiver for someone? Are. They doing well?

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@becsbuddy

Welcome to Mayo Clinic Connect @ksa230 ! I think you will really like this discussion; everyone is very open with their situations. And, may I ask, are you the caregiver for someone? Are. They doing well?

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Hi Becky,
I am the caregiver for my husband with FTD dementia. He has been physically declining rapidly over the last year. The FTD adds another emotional dimension, which is challenging. I am enjoying this service and appreciate everyone sharing their experiences.

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I think that once you get past the freak out panic of what is happening, come to grips with what must be done, it suddenly becomes easier to accept what your life has become and how it will progress. The million tasks exhaustion is still here but it is calmer now that I have learned to make the best of it and not worry quite so much. After a life of going at breakneck speed to accomplish it all, I am accepting that just moving along is OK.

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Is it OK to share this? I've noticed the cavalry is not coming and have resigned to that.

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I will also adopt that phrase "The Cavalry is Not Coming".....it fits many circumstances, I wish I had it 30 years ago.

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Wow!!! Prayers for you and my family who is suffering with this also. Thank you!! Thank you so much for these words. I can’t express what they mean to me. I needed to hear this.

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