The Long Quiet




Dear Friends,
I am quickly approaching ten years as a caregiver for my dear wife with late Stage 6 dementia. Alzheimer’s and dementia have long been known as The Long Goodbye because of the painfully long duration of the disease. No one knows how long their journey as a caregiver will go on, but I never imagined myself being locked into it for a decade.
Looking back, my long journey as a caregiver has gone through several phases. They roughly represent the stages of the disease itself. I have memories of 2015 and 2016 when my wife was still self-sufficient and self-aware; I have identified these time periods as Stages 2 and 3. Life was still mostly normal, with occasional signs that “something is wrong here” every now and then.
My existence now is best described as The Long Quiet. It is made up of years and years of no visitors, no conversations with my wife, very few phone calls, and very limited outings. The effort it takes to “go out and have fun” has long since ceased to be worthwhile. Most of my friends and family have moved on, except for the occasional phone call to check in.
Between feeding sessions, bathroom visits, showers, and diaper changes, my wife sits practically catatonic on the sofa “watching” television. Sometimes I play some music to brighten the mood, even though her response to music is also fading in this late dementia stage. When the television is off and the music stops, the quiet in this house is deafening.
There are no visitors. No laughter. No conversations. No intimacy. No smiles. No telephone ringing. No invitations. No communications. No response if I ask my wife a question or try to engage her. This Long Quiet phase has been going on for about two to three years, roughly her time in Stage 6.
Do you remember when you were a kid and you would give someone “the silent treatment” if you were angry with them? Caregivers are on the receiving end of the silent treatment for years on end. Marriages end when communication stops, but we must endure it because of “the disease.” Our suffering is not just changing diapers and lack of outside activity; we are persecuted by the disease day and night by this god-awful Quiet.
This is why I do not post here as often as before. Nothing is changing here. There is only silence for years on end. If my wife were well, I may have retired by now. There is no reason to retire now, as work provides some measure of conversations and normalcy.
Stay Strong My Friends,
Bill_2001
Comments
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Hello Bill, I recently joined this forum. I posted my summary a week ago or so but the wife was diagnosed in 2019. She’s very far along as I assist her with everything. I thought your cavalry post was spot on and I am going through that transition now. No one’s coming to help me. Just take what I can get. I do have a question for you though. My wife is now in what I call the jabbering stage. Constant, unending jabbering basically from the time she wakes up till she goes to bed. And now even through the night sometimes. Did you experience this? It’s like a Chinese water torture. Is the quiet stage worse than this?
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Hi Persevere,
Yes, my wife went through the jabbering phase, around Stage 4-5. Try playing music to give her an outlet to jabber/sing; music helped me get through it. As difficult as that was, the quiet, catatonic stage is no better. These behaviors all arrive as a sudden, scary new issue. I do my best to research the disease progression in order to prepare but reading and experiencing are two very different things indeed.
My wife is also losing agency, by which I mean she does not initiate anything she needs to do (eat, drink, etc.). This seems consistent with the Long Quiet I described, as I must prompt her and help her with even the most basic human functions at this point. Although I have acclimated, it is VERY depressing. My wife was once a vibrant, intelligent, active woman; this disease has decimated her mind so much that her very essence has gone missing.
If there is a bright spot, it is that all of these scary, annoying, and difficult phases/behaviors are temporary. As the disease progresses, you will begin to notice past issues have morphed into a new set of symptoms.
All the best, Bill_2001
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Hello Bill, Thank you for your post - I am new to this forum, and reading your post made me think back to when I was working and would come home after being away and wonder what DW was doing while I was gone. That was 6 or 7 years ago that I was beginning to wonder about the "little, subtle changes" that were happening. The vibrant, outgoing and busy DW seemed to be disappearing. I've not been 10 years, don't know if I'll ever get there. These are tough times. Thanks again for your post. BikingOldMan
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yes, my wife too was very active and vibrant. She had her own real estate company and was a connoisseur party and wedding planner. Seems like they all go through very similar stages but at different times. She too does not initiate anything anymore. Occasionally she implies she’s thirsty but that’s about it. I find too that as much as I’m suffering through this I still wish I could figure out how to bring some humor or satisfaction to her day.
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Bill, I think of you often. I think The Long Quiet is so heartbreaking. The realization that your loved one can no longer communicate coupled with friends and family not calling. You always know how to say what we’re all feeling. 💜
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Commonly Used Abbreviations
DH = Dear Husband
DW= Dear Wife, Darling Wife
LO = Loved One
ES = Early Stage
EO = Early Onset
FTD = Frontotemporal Dementia
VD = Vascular Dementia
MC = Memory Care
AL = Assisted Living
POA = Power of Attorney
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