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Spits his food out
I don’t know if this is a phase or just a progression of the disease. My DH is losing roughly 4 lbs. per week, and I’m sure it’s due to spitting food out. He will take a few bites, swallow, then the rest of the bites he spits out. What can I do about this? Nothing? I’m curious if others are dealing with this same issue.…
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Mom is 89=Alzheimer, Dad is 95=Pancreatic Cancer
Hello everyone~I just signed up with ALZConnected bc I am in need of experience, advise, support with my elderly "independent" parents whom I love so much! Here I go: My mother is 89 years old. May 2025 she was diagnosed with type 2 diabetes which has been challenging due to memory declining over the past several years.…
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Starting LEQEMBI next week need some advice
Just was diagnosd 4 weeks ago and start my Leqembi next weeek ….I hate needles and I would like some information on what to expect…Thank you so much.. I have had 2 TIA's and am a little worried about this whole Leqembi thing. Is the first time really bad or is it doable? thank you so much for this web site I had no idea…
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DH and my constant sobbing
I have read some of your posts and I feel terribly guilty about posting at all. My DH has had dementia for about three years and I believe he is in stage 6c. I'm trying to stave off incontinence by taking him to the bathroom at regular intervals. Being the toddler he is, there is no guarantee that this will work. So the…
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Bank Doesn't Recognize POA
Hi, What to do when credit union won't allow me to use the POA? I haven't contacted the atty who drafted it yet, full, durable $$ and medical/general POAs. So far my PWD can still come with me or talk to reps on phone but that could change anytime. USA SSA won't accept either- wondering what other agencies don't and how…
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VRBO VS Hotel
I know our traveling days are winding down but DH wants to go see his father in Florida. All his family live in Florida. I think it will be ok because we have family all around. The only change is his father is now in assisted living so we can no longer stay in his house when visiting. DH was very familiar with the house.…
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From the NYT: Blood tests for predicting Alzheimers
NYT Article shared. "Could a Blood Test Predict if You’ll Get Alzheimer’s? The tests could help to improve dementia care, but scientists say there are still some caveats and unknowns." There's a lot of nuance in this article. I think the main question for patients is: If you get a positive result, what do you do? It…
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Sundowning
Hello, I’m very new to this group and confused on this newly diagnoses of Dementia for my mother! We are still going through a lot of appointments and tests and we don’t have a actual diagnosis of what type of dementia my mom has but they are leaning more towards Lewy body because she has a tremor on her hand! My question…
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A New Level of Loneliness
I see that I had a post last year about the loneliness of living with a spouse with AL. Of course, the disease has progressed. I'm guessing that he is more stage 4 than 3. Really, who can tell for sure. We have a daughter who is not currently speaking to us as she works through some things. Exactly what things, she did not…
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Coping
I'm a caregiver for my Mom long distance. I don't have any support and I'm not sure how to cope anymore. She is declining and I feel she needs different meds because she is starting to show side effects. Not sure how to straighten this out. I've asked for help from docs but nothing changes or they are very vague on the…
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Sleeping 12 hours a night
DH was diagnosed two years ago, but has likely been impacted for 6 years. He was quite accomplished, so he was able to “cover” for many of symptoms as he declined. While ALZ runs in his family (grandfather, father, aunt, uncle, but not his brothers - yet) DH was able to make it to age 60+ without symptoms. For most of our…
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Affairs, Divorce, and Dodging a Bullet
Very long post alert. I only come to you all because even if your situation isn’t like mine, I know I will get wise (and hopefully not too brutal) counsel from the other travelers on this journey. I am 64, still working - now 2 jobs. My DH is 63 yo and is: ◦ not diagnosed with dementia ◦ Has multiple health issues…
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Grumpy Old Man
My DH is always mean to me. He thinks it is real funny when he locks me in a room. He loves to see me get angry. Always tells me I am fat. First thing in morning he says, Wheres my breakfast!! Like I am his servant. My 8 yr old grandson was visiting and it was constant teasing. MY grandson gets so confused that he is very…
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Helpful Resource
This site is an amazing resource of help and support for so many. I also saw a post in another section of a video on a particular subject. I found the information, presentation and vocabulary right on target for this audience so I thought I would share it here. It is offered just as another resource and supplement to this…
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Changing personality
This is my 1st time on here. I needed to vent. My wife has early onset and has mild cognitive impairment. She is still high functioning but has become very anxious. She gets riled up fast and takes it out on me. I am finding that I lose my temper when she is angry at me. Afterward, I feel bad cause “I should know better.”…
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Need to whine about moms house
Mom is a hoarder and her house is full. The house is an hour’s drive away. I have averaged one full 8 hour day a week there for the last three years. I replaced the carpet and sealed and painted the walls in the living room that had cat spray, I dug a path to the water heater and had that replaced and I got all the food…
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Mom in hospice care and seeing and talking to people
I hear this is common. Is it? My mom is in hospice care at her MC facility. I was with for a couple hours today. I would talk to her and she would answer back. She was more alert than she has been in a couple of days. I felt like it was a gift to be able once again to say something to her and she responded. It was mumbled,…
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Vascular Dementia and hyperactivity at night
My mom has been very active at night, talking to herself, calling me, can’t settle down etc. anxious any suggestions? she is on 100 mg of Trazadone, rispiridal, buspar, visteral and nothing is helping her to sleep! She was also recently diagnosed with stage 4 kidney failure from an arthritis medication side effect. i feel…
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Any of you dealing with sarcopenia?
My DH appears to be declining physically more quickly than cognitively. He has VD but both his mother and older brother died from alz, so he may have mixed dementia but not diagnosed. He sits most of the day and has for years. His legs and hips are weak and getting weaker, he has difficulty: rising from sitting, standing…
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Feeling helpless
My Mom has entered the later stages of early onset, 68 years old. Since the time change for daylight savings things have gotten worse quickly. Recently, she has had the police called on her for wondering the neighborhood and trying to enter strangers cars. This has all culminated in a fall and a broken foot landing her in…
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Brain shrinkage
Good Morning Warriors. I tried to research the subject of brain shrinkage and changes in facial features. There doesn’t seem to be much about this. My DH is gaining weight in MC facility but his face features are changing dramatically. In particular, his eye sockets are deepening. His cheeks are also sinking in. He has…
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A letter to Memory Care Center managers
Dear Mr. Memory care manager, I have been working hard these last 50 years and always setting money aside for retirement. Now I need that money to pay for memory care for my DH. Memory care is my vacation, my world tour and my retirement all rolled into one. Today I arrived at my Dh's "care suite" only to find that yes you…
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Newbie here trying to navigate this
Hello, Not formally diagnosed yet, but my pTau-217 LabCorp test showed a .37 result. I was already diagnosed with MCI last March. My pTau test last year resulted in a .18 which is right at the cutoff, thus the retest. So somehow my levels doubled in a year. This shocked my doctor who seemed to poo poo my concerns up until…
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Brain swelling (edema) on Kisunla
I'm hoping that others who have had brain swelling as a side effect of Kisunla can give me some ideas and some hope. I've had a really easy time with Kisunla (Donanemab) since I started in August, and all of my MRIs were perfect. There was break in MRIs from month 5 to month 7, but when I had my MRI last week in…
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Processing DH's Dementia Journey and Recent Death
My DH graduated to heaven recently after seven years of moving through the different stages of Alzheimer's. After living with anticipatory grief, this final ending of our earthly relationship has been very hard on me. He was the center of my world. I spent at least a couple of hours every day for the past year with him at…
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Is it time?
I've been caring for my LO for 3 years. His progression is getting worse. I was not prepared for this, nor what is to come. Incontinence and it's a battle to get him changed. Showers are hard. Relieving himself outside of the bathroom. Wanders at night, gathering items, hiding items. He is not aggressive or combative at…
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Hoping to Start an Ongoing Conversation Space for Those Living with Dementia
Hi everyone ,My name is Kerry. I’m living with dementia, and like many of you, I’m navigating a lot of feelings and emotions. I’ve reached a point where I’m really craving connection with others who understand this from the inside, not as caregivers, not as observers, but as people living it every day. I’ve noticed that…
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Today’s Question?
How could DH with VD smell the bread baking but cannot smell the urine soaked clothes he is wearing? Just curious 🤷🏻♀️
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I failed as caregiver today
Yesterday I picked up a nasty cold and had a really rough night last night trying to sleep. This morning my wife (who has Alzheimer's, stage 5) had another emotional meltdown. Partially accusing me of of keeping her here at our house to kill her or some such nonsense. I am at low ebb, having little to no patience this…
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Sundowning in the Morning?
A question for the community, My DW has been waking up the past week or so with a continuation of the sundowning attitude and demeanor she was experiencing the prior evening. Is this a common experience others have experienced with Alzheimer's? Is this an indication that my DW condition is in further decline?