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What's your pleasure?
This is my first post! This year has been very hard for me. I moved in with my parents in February, got them well enough to move to AL in April. My mom never fully recovered from the shock of moving and she died in June. My dad will go into MC next week. Along the way, I've tried to find a few moments, a few things to…
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How to support my stepdad as primary caregiver
Hello. I am new to this platform. My mom is in Stage 6 of Alzheimer's. My stepdad is her primary caregiver. I can see that he is in over his head and is stressing out. But he is shutting out ideas for support, saying that he can't handle any more information. He is trying to do everything himself, and I can see the…
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Feeling Very Alone
Hi everybody! I hope everyone is having a good day/night. I am 24 and the main care taker for my mom who is 59, she was diagnosed with Alzheimer's back in 2022. The first year since her diagnoses had been pretty uneventful, no huge changes besides getting her disability approved. She had already stopped driving and working…
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I am very sick with covid DW also infected. Help with ER visit
my DW has rapid Demetia, she is in late stage. Which is challenging enough, trying desperately to get some respite relief which I have been granted 12 hours a mont( which are now cancelled due to the Fact, we both now have Covid… DW doesn’t have the severity of symptoms as I do. I am trying to get to the hospital ASAP for…
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MIL moved in without warning, without a plan
Hi - I'm new here - and I'm feeling so everwhelmed. So my MIL has lived alone for the past 20 years- the past 5 she has been declining- we unplugged her stove- put a lock on the door so she couldn't go downstairs - etc. My husband is a procrastinator - we finally went to a lawyer last week (as for years his mother told him…
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Respite care services Denver, CO?
Hi- new to this space. My mother was recently diagnosed with beginning stage Alzheimer's and capgras. My father is the primary care partner at the moment and he needs respite. Does anyone know of an assisted living facility in the area that will do short term respite care? Thanks!
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Need help for my mom
My step father is caring for my mom who is quite advanced, she doesn’t really get any interaction with anyone, they live in a small town in Nevada so not many resources there. My step dad is slowly losing it with my mom, short fuse and all, he wants to put her in a State home but mom still recognizes everyone , just has a…
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First-Time Poster Requesting Support
Hello to you all. This is my first time to post in the forum. I have been reading a few posts that may help me with my father. At his most-recent visit with his neurologist, we were told he was at stage 6B of Alzheimer's. We have been living with what we were told was dementia for several years, and the Alzheimer's…
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Emotional Abuse
Hi there, This is my first post and, I'm really desperate for help or advice. I am moving cross country to care for and support my mother who was just diagnosed with Alzheimer's (though, I think this has been progressing over the last several years). I am doing everything I can to help her and it never seems like enough or…
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Asking for help( caring for a loved oned showing signs of dementia)
Hello everyone, Me & my mom would like some advice. We are currently caring for my grandma & she has been showing signs of dementia. We have been to multiple doctor appointments, just waiting to hear the results. Even though she hasn’t been diagnosed, we’re pretty sure it’s dementia being that in runs on her side of her…
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Early onset VD/Alzhiemer’s
Hi all, glad I found this community. I haven’t met anyone I can relate to about my situation and it would be nice to have someone to talk to that understands. I brought my mother to the hospital the day before her 59th birthday because she was barely able to walk, could only move one eye, stroke-like symptoms. When she…
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When he can't stand up anymore
My dad is 81 with dementia and heart failure. He is in hospice at home. My mom (81) and myself ( I'm 50 and have severe treatment resistant depression and physical disabilities) care for him. Twice a week a nurse comes to check on him for 15 min. He is no longer able to walk; he can stand briefly with a walker so we can…
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pity party day, week, month...
DH was diagnosed with EOAD (age 61) November 2021 after a lumbar puncture. He was MCI at the time. Currently he his solid stage 5 with stage six leanings. He does not shadow, he is velcro. Can't follow simple commands or remember anything for longer than a couple of minutes. Still continent, but the hygiene is out the…
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Where do I Start?
I need to figure out where to start. I’ve got to have some extended “me” time. He drives me crazy with repeated questions, IPhone issues, wet pants, confusion, deliriums, pacing, rubbing his hands, running interference with his truck (I don’t let him drive) and scammers. My life is exhausting. I’m falling into the abyss…
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Alternatives to Driving
Hi Everyone, this is my first post here. I read a lot of the past conversations on driving, but have what I think is a twist on the question. My best friend's husband was just diagnosed with Early-Onset Alzheimers in his 50's, and like many is having problems accepting that he can no longer drive. My question is about the…
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Books that were recommended to me
The Social Worker, Tessa, at The Memory Center Clinic (Dept of Neurology) at the University of Chicago Medicine recommended these 2 books to me, at Ray's appt last Fri. Have any of you checked these out? I read the reviews over at Amazon.com. I ordered these. I'm a retired dinosaur RN. "Travelers to Unimaginable Lands" by…
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Men’s support group
I know there is a men’s support group called Light Lounge, found in a 2022 discussion thread. Are there any other men’s support groups you have knowledge of?
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New Here: Looking for support/community for "secondary" caregivers, extended family
Hi Everyone. My first time here. My sister in law was diagnosed with early on-set Alz about 16 months ago (after about 4 years of misunderstood difficulties) and seems to be progressing very quickly. I'm with her at least two days a week as a secondary caregiver to 1) spend time with her and 2) help take some of the…
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New Article Sent by my CELA: 5 Medicare benefits consumers should know about. TRUE??
Hello fellow caregivers, My CELA just sent me an article titled, "Alzheimer’s disease and dementia care: 5 Medicare benefits consumers should know" because she wanted me to know that it looks like Medicare Part A will pay for up to 35 hours of in-home care per week for dementia patients who are homebound and require…
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Suggestions PLEASE
Hello everyone! This my first post, as a matter of fact, this is the first time I am dealing with someone with dementia. I am overwhelmed to say the least. I recently came to stay at a shelter, as I lost my house. This was 2 months ago. It's a small shelter, at present, there is just myself and another person, who has…
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Looking for my Care-Giver Peers with Spouses with Early-Onset ALZ Denver Area
I am a 60 year old man living in the Denver area. My wife was diagnosed with early onset at age 53 in 2020. I have attended our local monthly group but it gets so crowded and rarely is there enough time for serious discussion. It is emotionally draining and hard to find coverage so I can attend the meetings at the time…
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Mother not cooperating with maid
My mother ,aged 66,is not able to go to washroom by herself We have maid,who helps her, recently she is not cooperating with her as well. Other than my sister,she does not allow anyone else to be with her. Need suggestions....to deal with mother Also,she is hallucinating....she looks at herself in mirror and gets hyper...…
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Not sure what to do?
Hello, my name is Mary and I moved in with my mother in January and have been her primary caregiver since then. And to put it nicely I am exhausted. I moved in as my brother was moving out after about a year. My brother's wife abruptly filed for divorce in December of 2022 and he was forced out of him home within 48 hours…
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From The NYT: The Ethicist- Spouse with Dementia
I have so many thoughts on this starting with "has this columnist ever lived with a PWD?" https://www.nytimes.com/2024/06/14/magazine/husband-dementia-divorce-ethics.html?unlocked_article_code=1.z00.2GoA.8KLGpmxh2ufJ&smid=url-share
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Therapeutic Lie #2
Hi everyone! This is kind of a continuation of my last post. I am trying to get my mom (60 with ALZ) in to an adult day care program, and it did not go well. Well, we didn't even get to the day care place. I took all of your guys' advice about saying it's a place where I volunteer at and have some friends I want her to…
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How do you process your thoughts, feelings, and slow burning grief?
Hi everyone. I’m new here. So glad I found this online community. The last three years have been super intense. From my mother getting diagnosed to losing her job to hiring at-home care, and the moving to assisted living in Jan 2023. This is a short summary, of course. But now she needs 24/7 supervision and it’s just SO…
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Therapeutic Lie
Hi everybody! I was looking for some advice on how to explain to my mom (60 with ALZ) the idea of starting to go to an adult day care program. There’s this wonderful program that’s 5 minutes away from us, in a senior center that my mom is familiar with already because her mom used to go there. I’be recently heard the term…
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How To Balance Life
Hi everyone! Hope you and your LO’s are well. I have been having a lot of problems having a proper “work-life balance” for lack of a better term. My mom’s (60) diagnosis and required care takes up all of my energy, thankfully she’s still able to move around and shower herself and use the bathroom on her own, and those were…
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Flew home and found mom in self neglect
I am the youngest of 7, and my mother’s only girl. I’m the favorite and so I have the best relationship with her. My mom is 74, and I noticed something was wrong last year when she was showing some short term memory loss, not answering her phone, and making excuses to not fly to Colorado to visit her kids. Saying she was…
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On the advice of my therapist
I have a habit of minimizing or stuffing down feelings and emotions. My therapist has given me the assignment of telling someone about something I am struggling with. Not to look for a solution but as a way to validate the experience. And so… I have a great deal of resentment and a feeling of loss of self. DH was diagnosed…