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Still waffling on MC placement
After touring MC facilities for my plan B, I started thinking that maybe DH would be happier and better cared for if he was there. There are a few reasons for this which I won’t go into but I haven’t made a decision yet. I am not good at being decisive - ironically that was one of the things that attracted me to my DH at…
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Just need to talk to my friends (210)
I started this months new thread, 210, but entitled it 110. I tried to delete or change it but didn't work. Maybe this will. The other one is saved somewhere. So sorry for the confusion.
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Social Scientists, We Are Here
As I read through the threads on here and, like all of you, find great value and comfort from this forum, I am struck by the discrepancies between our real life and what is described by most (I am sure there are exceptions) articles or studies. As I began our journey, the medical community could offer little, if any,…
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Home health care
I'm 70 and in reasonably good health, some issues that are well managed. DW is 67, about 3 years or so in. I would say moderate stages. A fair amount of urinary incontinence, needs assistance with bathing and dressing. We have an adult daughter who's doing all she can to help us. I cook breakfast every day, and either our…
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Feeling alone and lost
I have not got a diagnosis for my husband yet but its so difficult as he used to do so much and now he jist sits and I can't get him to do anything . I have been finding all kinds of stuff in trash cans almost daily I feel like a dumpster diver. if I asked him why he say I dont know and just like he didn't do it. I been…
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New to this. DH with MCI due to AD
Hello. I'm so glad I found this support. My DH, 66 yo, was diagnosed with MCI due to AD in July 2025. I noticed ST memory loss for about 5 months prior, had his PCP do a MOCA where he scored 24/30 which led to Neurologist, PET (significant beta-amyloid plaque), pTau .33. He failed Aricept due to GI issues; is now on…
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Anyone interested in a zoom meetup?
Would anyone be interested in doing a Zoom meetup in the evening? I ask because, at least where I am, there are absolutely no caregiver support groups that meet outside of normal working hours. (When my mom's doctor recommended one to me and I told her I can't because I have a job, she was confused and asked "You couldn't…
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The Stage 8 Club
I first learned the term, stage 8, on this forum just a few days ago. Never new what i would call my life after she passed. It has been a little over three weeks since my dear wife left me and the family. It was a long eight year journey but thankfully she did not suffer physically or by some other health condition and she…
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Sundowning
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living the movie Groundhog Day
My wife and I have had a wonderful 40+ years together. Recently, the neurologist diagnosed her Alzheimer's as "early moderate" stage. I believe the moderate stage began during the past year. The biggest change so far (in the moderate stage) is not greater loss in memory (although there is some). Rather, it's behavior…
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Trying to keep my sanity
Hi. I'm relatively new here. My DH was diagnosed a year ago with Alz., but I noticed changes about 3 years prior to diagnosis. I'm not totally unfamiliar with Alz. as I was my Mom's advocate in her last few years with it. She has passed, but I thank her for the practice I received ... not that anyone wants practice or any…
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Do we ever sleep?
Here it is at 4 am. Been up since about 2:30 am, not unusual at all. As I scroll through the threads here, now and then offering my two cents, I noticed the times of postings. Amazing number seem to be posted during the very late hours of the evening or during the overnight hours. Do we, as caregivers, ever sleep? I know…
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Alzheimer's and Finances
My 84-YO dad has Alzheimer's and is living independently still. He lives close to me, so I see him every day. As most of our loved ones, my dad does not recognize he has a memory problem. I am his POA, Guardian, etc., but he honestly doesn't remember us putting all that in place years ago. How did everyone take over the…
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Care home wants more meds because of aggression
My DH has late-stage early-onset Alzheimer’s with aphasia. For his safety and because I work full time, we had to move him to memory care 10 months ago. Before moving he would sometimes strike out at our home caregiver. In memory care he became aggressive when exit seeking and during grooming. We tried medication but ended…
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Too old for this/too young for this
Newly diagnosed spouse of 40 years. He’s in denial, I’m in panic mode and end times mode. And it’s only just started. Twist? He doesn’t want any treatment. Anyone have any experience with no treatment? Or know how it may go?
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Refusing to take meds
This is a new problem for us. My DH is pitching a FIT when it’s time to take his meds. He absolutely refuses to do so. I’m probably not doing this right, but I beg him to take them for his dr’s sake. Last night I begged him to take them for Cody, that’s the dog. He did. He started chewing them a few weeks back, so I…
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Grieving
I find I am grieving the intimacy that we used to have. I tried to hug him this morning he said to me, I don’t love him. I felt like it tore my heart right out of my chest. We have been married for 67 years. It is my DH. I find myself often in tears I’m 84. I feel like I live in the house alone. He gets angry so easy I do…
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Anosognosia—When People Don’t Realize They’re Impaired
The topic of anosognosia comes up regularly, particularly for people who are new here. It's confusing and confounding when your LO can't see their own impairment. I think this article is a good introduction. I hope it's helpful. People who are experiencing dementia often refuse care. However, most of the time, it’s not due…
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Rehoming
How do I help my mother understand she is living with me now and can no longer go home?
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Help with restless, sleepless nights
At bedtime, my wife will sleep for about an hour then will become restless and repeatedly get up and down, then roam around the bedroom and upstairs all night like a zombie. She has moderate/late stage Alzheimers and takes risperidone (Risperdal) but doc is weaning her off and will replace with Geodon soon. She also takes…
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Leqembi Infusions
My husband is in early stage Alzheimers and our Neurologist recommended Leqembi. After much discussion my husband decided he wanted to try it even withe the serious side effects. After 3 infusions they did an MRI to look for side effects (brain bleeds). All was good. After the 5th infusion they repeated the MRI and it…
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Losing patience
My brother who has power of attorney just brought documents for my mother to sign to receive some payouts from life insurance and the military. Since yesterday afternoon she believes that she got a deposit and has been pestering me about paperwork. I suffer chronic illness. I provided care for my stepdad as he died of…
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Leqembi infusions
Hello. I'm new to the group. My husband was recently diagnosed with MCI due to AD, 66 yo. + APOE 4. Needless to say, we are devastated. He's had mild memory loss for about 6 months. Tried aricept but had terrible GI symptoms. He's been tolerating Namenda. I haven't noticed must improvement with his ST memory. However,…
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Is neuropshych exam worth it now?
DH was diagnosed with early AD via PET. We have upcoming scans to see if he's a candidate for the infusion treatments. We have a neuropsych exam (the 3-4 hour one) scheduled. Is it worth it to still get it done? Costs are rising and I'm not sure the value. Would love to hear some opinions.
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Considering move into Assisted Living for both of us
DH has AL, probably stage 4. He is 90 and I am a couple of years younger with my own health issues but still an active senior. Our children are concerned about 2 things: firstly what will they do with their father if I am suddenly incompacitated or die, and secondly they see the strain this is putting on me. In all…
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So over this...
I hate my husband. I've been thinking this way for a long time and just felt like I needed to say it. I hate everything about him and this disease. I have no help, so the last 7 years have been very difficult. I have some in home help starting soon. Sorry to burden everyone with such a negative post.
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Our journey together.
We are in year 3 of my wife’s battle with Early Onset Alzheimer’s Disease but I still feel this way with her. To My Beautiful Wife Each time I look at you, I just smile to myself and think, You are perfect just the way you are, my one in a million. You are my special kind of love that makes me realize that life gave me the…
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DH always wants to leave the house
All day long, DH is constantly wanting to “get going”. He is fixated on walking a specific route in the neighborhood. We walk the route, stopping to talk to anyone we see (which is another challenge), we come home, change out of our sweaty clothes, then he says “are you ready to go?” This goes on ALL DAY LONG. He doesn’t…
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Adjustable bed suggestions (attached control)
Hi, I'm trying to find an adjustable bed for my mom, who lives with Alzheimer's. They all seem to have remote controls, and she really needs something that has only a few buttons and is hardwired (attached) to the bed. Otherwise, the remote will quickly go missing. Has anyone found a bed that's working well for them?
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How long can show timing last?
I was purposefully eavesdropping on my DH's phone conversation with his Mom because that's the kind of person I am now. And I was thinking how good he sounded with her. But then I heard him tell her about an argument he had with his sibling that did not really happen. He did this about six months ago before his diagnosis,…