Normal household noise becomes intolerable???
My DH is mid to late stage 5. He's still able to take care of his daily needs, but he needs help with most tech stuff, no longer drives and of course has a hard time having a conversation as he grasps for the words. He can't really follow most conversations, but gets upset if I slow down what I'm saying "Don't talk to me like I'm am idiot!"
Lately he gets frustrated, sometimes downright angry, over what I consider normal household noises.
Such things as me opening the freezer drawer and rummaging in there for something for dinner is me banging around in the kitchen. Someone closing the bathroom door he feels it's being slammed.
Neighbors talking in their yard is "why are they shouting?"
You get the picture. It's driving me nuts and I'm walking on eggshells trying to be as quiet as I can.
Yet, he is hard of hearing, but of course doesn't wear his hearing aids and I've given up on trying to make him. So a lot of the time I get the "I can't hear you when you're looking away from me!"
I do know that when he's focusing on a task, like even playing a game on his phone, any other noises irritate him as he can't focus.
I guess I'm mostly venting, but if any of you have experienced something like this did you figure out anything that helped?
My heart goes out to all of you on this journey. Hugs.
Comments
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I wish I had some helpful comments or tips. My Husband is not that advanced with his disease, but he’s getting there, of course, and I noticed that he also seems to be puzzled by what I considered to be normal household sounds. And these are things that he’s heard for years but he almost . Mine doesn’t have hearing aids and I’m not even gonna battle to make get them because I’m sure like your husband he won’t wear them. Go ahead and vent away. I just this discussion group and I hope it’s gonna help because I do need a place to vent my frustrations fears irritability.
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I agree, we all need to vent, or cry or scream or just come to know we're not alone. This is a wonderful space for that and I'm so very grateful.
I've yet to become brave enough to reply to most posts, but I certainly do askfor advice and vent plenty. :)
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My spouse did not have this symptom, but I've spent time thinking about the way we filter noises. It's a brain function. My dad gets upset about all those things if his hearing aids have been broken for a while and then he gets them fixed—his brain is no longer used to filtering out the noises that are irrelevant.
Sometimes I read about hearing loss and the way it correlates with dementia. I've read people suggesting the correlation is about changes in communication, but I think it has more to do with the brain not functioning to filter noises as it normally would.
I don't have any suggestions, and I assume he wouldn't wear noise reducing earphones or headphones.
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My DH went through that but it seems to have diminished now that we are coming to the end of stage 6/ starting stage 7. The worst was when I was loading or unloading the dishwasher. Noise intolerance is very common and it is very hard for them to process what is going on around them. Hang tough! Glad you vented
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Thank you all for your support. I really appreciate it.
These are the times that I find myself hoping he'll slip into the next phase and not have this intolerance any longer. :(
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Thank you for this jgirl. My DH is the same driving me nuts, the dishwasher particularly, next door neighbours talking, the dog barking. I think he might be slipping into stage 7 but I’m not sure how to tell all I know is things are getting harder.
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I'm so sorry to hear you're dealing with this too.
I don't think my DH is that far along, but I suppose certain symptoms can hit at defferent times for different folks.
I'll be thinking of you as you journey along with all of us. Hang in there, stay strong (like we have a choice right?) And don't forget to be kind to yourself too.
Hugs.
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To all: I found this info from Natalie Edmonds:
Hearing Changes in DementiaNormal Aging vs Dementia Related Hearing Problems
Many older adults experience hearing loss. They ask people to repeat things, turn up the television, or have trouble in noisy places. These are usually issues with the ears themselves and often improve with hearing aids.
With dementia, the ears may work fine. The challenge is the brain’s ability to interpret what it hears.
Your loved one may hear your words but be unable to understand their meaning. They may listen to the sound but cannot process the message.
Common Hearing Related Changes in Dementia
Difficulty understanding speech
Especially in noisy environments, the brain struggles to separate important sounds from background noise. Your loved one might be able to hear the waitress speaking, but their brain cannot process her words.
Sound distortion
Sometimes voices sound too loud, too harsh, or confusing. This is why someone with dementia may accuse you of yelling at them even when you are speaking normally.
Trouble following conversations
They may nod politely while talking to you, but moments later seem confused. The nodding was not understanding. It was an attempt to keep up without revealing their difficulty.
What You Might Notice
• Repeatedly asking what, even though their hearing seems fine
• Turning the television volume up extremely high
• Saying things like stop yelling at me when you are speaking gently
• Avoiding conversations because they feel overwhelmed
To help with this, try reducing background noise, facing your loved one while speaking, and breaking information into shorter, simpler phrases.
Here is link to full article on how dementia affects the 5 senses:
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My DH experiencing/exhibiting many of these as well. Hang in there everyone! The next change in this terrible/heartbreaking disease is right around the corner!
Hugs to all. 💝
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@shiawase12
One thing I noticed with my dad was that as he progressed in his dementia, he began to share significant symptoms with a person who has autism. It was not just the lack of empathy, poor executive function and inability to use language pragmatically he also developed significant sensory issues. His hearing was poor and sound sensitivity wasn't an issue for him but processing taste, light, smell and especially touch (temperature and textures on his skin) became a bug issue.
Another thought is that spatial reasoning is a brain function that tanks fairly on in the disease process. I wonder if in your DH's case if his auditory processing is becoming an issue. It might be worth trying a noise cancelling over-the-ear headphone.
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My DH is also hard of hearing and rarely wears his hearing aids. He doesn't find noise intolerable but he often is surprised/startled by a normal household sound and cannot identify what it is. The hydroponic watering system comes on every night at 10 and invariably he will jerk his head around and ask what was that. It appears to me that the problem isn't the particular noise per se but the inability to figure out what it was. TY to JGreen for posting Natalie Edwards remarks. Very helpful.
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My dad (stage 6, in MC) has complained of noise for more than a year now. A door closes: “Why are those people banging around?” Someone speaks: “Stop yelling at me!” It is a processing issue, I think, and he hears noises as threats—although sometimes I have seen caregivers speaking to him at an excessively high volume, so he is not always wrong about “yelling.”
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My DH is having similar problems. If he hears a banging or knocking noise he says someone is knocking on the door or he says “what’s that noise” if the refrigerator ice maker drops ice. He also complains that most restaurants are too noisy and he hates the ones that play music. He says most music is just noise but we do go to concerts. When there he wears ear plugs bc he says the music is too loud. He’s also hard of hearing but won’t wear his hearing aids.
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Great comment and information. My DW has the exact symptoms mentioned, accusing me of yelling when I am speaking normally. Some days we whisper to each other for the morning. Closing a cabinet door or the like gets me a big SHHHH be quiet! It's usually done by noon. It's one of the more tolerable symptoms for me. The whispering seems a little more intimate anyway.
I'm not a Dementia Careblazers support group member but I have watched a lot of the YouTube videos and found them very helpful.
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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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