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In fact, I'd bring up the legal paperwork with her neurologist tomorrow. You may have to be blunt and say that you moved her in next door to you but that you cannot be expected to take on the responsibility of caregiving for her without the authority especially not if dementia is on the horizon. Insist on not being kept in the dark.
we need you in here!"
If the doctor is getting nowhere with a cognitively challenged patient, they will often come and get you.
This is something you can ask the nurse.
I'm waiting by my phone now so I don't miss the call from the nurse, and I will have things written down for the doctor. I think that's all I can do right now. Hopefully the doctor can offer some guidance. My mom can't fake as good as she thinks anymore anyway. I ignored lots of red flags in recent years but that was more my own denial as a defense mechanism because this is my mother, but this doctor won't have my emotional handicaps so should recognize things.
Thanks for your response. I know I ramble a lot on this site because I am still struggling to accept all this and I'm still so afraid of the future. One of the things I know I need is to have a good neurologist on board and this appointment is the first step. I wish I didn't feel so anxious about it.
Honey, ramble on. We don’t mind! This is very upsetting. I’d be upset too. It’s important to get proper results.
I moved my 85 yr. old mother in with me in March of 2018 after my dad passed away in October of 2017. I had mom evaluated by the insurance company that I set up for her shortly after moving in with me and learned she had already been suffering short-term memory loss, which truly upset her to the point of tears. When the evaluator told her, she began to start crying and I immediately asked her, what's your mother's name? She replied correctly and, I told her, You remember what is important and nobody cares about a hamburger, peach and a pencil. That comment lightened the situation and I gave her a hug.
Later last year on October 20th, I took my mom to the movies and noticed she was quietly but repeatedly asking me the name of the movie. I simply responded each time and figured she may have been tired and that is what caused the excessive questioning. However, when we exited the theater, she asked me where the woman whom brought her there was and if dad was back at the house sleeping. She was also referring to people and family members who were clearly not there and deceased. When I explained that I was the one whom brought her, she replied, "No, you met us here." I asked her if she knew who I was, and she replied, "Of course I do, you're XXX." Mom thought I was her sister, whom died more than 15 years prior and I realized later that the dad she was referring to was her own.
I took her to dinner thinking that perhaps she was tired but, strange and inaccurate comments and questions continued. When we got home, I called her doctor and could not get an appointment early enough. I kept correcting mom in the beginning but there was no rationalizing with her - she was in denial and utterly confused. She did not remember my dad passing and refused to believe it. Everything coming out of her mouth was a confused fantasy and inaccuracies.
I ended up telling her the following morning that I'd heard from dad but he did not tell me where he was and simply gave me an address we had to go to. Of course, it was a made up plan for me to get mom to the emergency room of a neighborhood hospital. Her doctor could not see her fast enough and I knew something was seriously wrong.
A nurse evaluated her upon arriving and they admitted her immediately. I stayed with mom in the hospital because I did not want her to be frightened or further confused. A CT scan, head x-ray and other tests revealed that mom had suffered minor strokes, which affected her brain. The strokes basically launched her into moderate stage dementia within the span of a movie.
When they released her, they basically sent us home with no preparation for me on how to deal with someone whom had dementia. I went out of my mind for a few days until I arranged for an aide to come in and help me. No one in the hospital told mom that she had dementia - they told me.
After the hospital, I took her to a different neurologist because I found the ones in the hospital to be inadequate and dismissive. I went to that appointment with her and the aide. When mom asked me why she was there, I explained that it was just a check up to make sure she was okay and that I was being checked out too. I took steps to speak to the doctor, nurses and any assistant(s) so that they would not say the word "dementia" in front of her because mom was not aware or accepting of it. Thankfully, with a lot of work on my part, they complied. I did not allow them to speak to her without me in the room.
Once the dementia meds kicked in, things got a little better but, of course, dementia is not curable. I downloaded a book from Amazon called "The 36-Hour Day" as well as others to help me become more enlightened. The underlying advice in most seemed to be, keep them calm, happy and safe. Don't point mistakes or inaccuracies to them if it makes them feel bad or unsafe. Pick your moments. Some moments may be more lucid than others. .
My mom had her appointment- I updated on that here: https://www.agingcare.com/discussions/neurologist-appointment-and-more-testing-447319.htm?orderby=recent
It sounds like your mom's dementia is also vascular dementia. I'm learning that the progress is different than Alzheimer's in that decline happens in steps, that can sometimes be very rapid because of mini-strokes. It sounds like your mom had a significant step down at the movies. Thankfully she was with you when that happened and you were able to keep her safe.
Do you mind telling me what meds your mom got where you saw some improvement? My mom is already on meds to control her BP and cholesterol, and also aspirin. The neurologist didn't suggest any additional meds at this point, but did write an order for physical therapy and more neuro-psych tests.
How is your mom doing now? Is she able to take care of her own hygiene and feed herself? I'm glad that my mom is still able to function independently in those areas, but the mental decline remains a huge worry for me. I will check out the book you mentioned, because like you nothing prepared me for dealing with dementia. I've learned a lot in the last six months from reading online and this site, talking to my own doctor and now this new neurologist who thankfully was excellent with my mom.
I like the advice of keeping them calm, happy and safe. I will always keep my mom safe. That's why she is here. Now the calm and happy.... I try my best but those two are challenges. My mom has always been a negative person and also narcissistic so keeping her happy is almost impossible. I get moments, and good days here and there, which I've come to cherish because they are rare... but in general it's a challenge. We're finally getting some sun and warmth in my area so I'm taking her to sit on the beach for awhile today. This will be her first trip to the beach even though we live a 3 minute walk from the coast. I hope it will go okay.
Best wishes to you and your mom.
Sendhelp has a good point if you can just get mom to her appointment would be a good start and like she stated it is hard to fool a specialist!
With her, they did want to evaluate her alone because otherwise they look to the family for cues. It’s hard not to pipe up with the correct answer so if she doesn’t know , just smile or don’t look at her, ie pretend you are looking at your phone or something.
I worked in medical offices for years and it was amazing the 'stories' a patient would tell us, thinking they could pull the wool over our eyes.
I see it with my Dad, who is doing incredibly well at age 90. All his shoes are slip on, because he cannot bend down to do up laces anymore. If bits of paper fall to the floor, he cannot pick them up. He has a gripper tool for larger items, but it does not work for flat paper. Dad's long term memory is incredible, but he sometimes gets words like Yesterday and Tomorrow mixed up. He knows what he means, just cannot find the correct word.
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