Mild Dementia, Delirium, UTI, Low BP & destructive. Last week a Neurologist diagnosed mum with mild dementia but currently suffering delirium. She is getting recurrent UTIs and is just about to finish the latest batch of antibiotics. Took her to doc on Tues because she was so tired and just not her *normal* self. Her blood pressure was extremely low so we went to ER. Where BP went up, but only when laying down, sitting and standing it remained low. They did CT & blood work all was A OK. This morning I found she'd some how gotten ahold of the tylenol, she said she'd taken 5 and 1 was left in bottle. There were alot more in the bottle last night, so I of course freaked out thinking she'd taken 50 not 5. BUT THANK GOODNESS turned out she had taken only 5. While trying to come to terms with having to re-secure meds, I find that she had been moving around my *stuff* in the bathroom and had tossed out some of my makeup and makeup remover tissues. This is the 2nd time I have found items in trash basket. Once found her distroying an item just purchased, she doesn't know she's done any of this. Is this part of dementia?
I am literally at a loss. She is continually moaning and groaning, always in pain, though according to the doc there is no basis for the pain, he says its muscle related. She isnt eating again, and its like pulling teeth to get her to drink fluids and take her meds.... other than pain related ones..... does this sound like *mild* dementia? I don't know what to do, am I helping or hurting by caring for her at her home? The latter is going to change as I live in CA and she is in MO. I was planning to bring her back to CA with me.
9 Answers
Helpful Newest
First Oldest
First
Pam you said what I had already been thinking, that flying, or any form of major change probably wouldn't be for the best. But how do I get her back home?
New2demenia.. that is another issue for us the dang expense.
ADVERTISEMENT
This is a horrible disease.
I moved into my mom's home to become her caregiver. BIG mistake. If you decide to move you mom into your home make sure you have caregivers in your home and respite care for yourself.
Assistive Living facilites would be a wonderful option, but they are EXPENSIVE. I wish my mother had not made so many finical mistakes late in life so that she can afford one. But that's a mute point with my head strong mother because she refuses a caregiver and is hell bent on staying in her own home.
The neurologist might have said "mild" because your mom was sitting there, pretty as a picture, answering his questions correctly. She was putting on a show. But it doesn't sound like "mild" dementia.
And while there are phases of dementia don't get too hung up on them, they're more of a diagnostic tool than for personal reference. There are places on the internet that will specify phases of dementia and your mom may fit into one of the phases or 3 of the phases. It's not black and white.
And I agree with Pam, your mom should not be on an airplane and driving her across country should be a last resort as well.
Her appetite may be off because of the antibiotics. You will have to wait and see. She can not be left alone anymore.
http://www.aplaceformom.com/dementia-care/dementia-stages
As you read how dementia progresses from mildest to very severe, the behaviors you can expect and the care needed, ask yourself if you're willing and able to participate in the journey with her in your home.
Mom would fall under "Very Severe Cognitive Decline" and sinking fast. It has become darned near impossible to care for her at home.