Geriatric Psychologist


Hi,
My mom was recently diagnosed with Alzheimer's. She is still in stage 1 and can be independent. Has anyone gone to a geriatric psychologist and did it help?? I appreciate all the help I can get. Thank you!!
Comments
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@malibu2155
I'm not sure what you're asking in terms of help.
A geriatric psychologist for neurocognitive testing to determine what sort of dementia she might have and tease out the areas where she will need assistance with her IADLs?
Or do you mean a geriatric psychologist for talk therapy?
Or do you mean a geriatric psychiatrist for management of psychoactive medication?
When you say she was diagnosed but is still in stage 1; is this what her doctor told you? IME, physicians tend to use a 3-stage model based on treatment protocols whereas most caregivers/family use the 7-stage model which aligns with care needs.
To answer you question. Dad did see a neuropsychologist for some testing as part of the diagnostic process. His symptoms and behaviors didn't neatly align with a specific kind of dementia, and this helped confirm his mixed dementia diagnosis.
Like most PWD, dad had some anosognosia (can look like denial but is in fact an inability to recognize deficits) and such poor reasoning and memory that talk therapy would have been wasted on him. YMMV.
Dad did have depression, anxiety and aggressive behaviors. He saw a geri psychiatrist for medication to dial that back. This doc was far more useful to us once we had the firm diagnosis.
HB1 -
Welcome. I’m a bit confused about stage 1. I will attach a staging tool that is very helpful and this is what is generally used when referring to stages on this site. (Not that one is better just so everyone is on the same page). Since you said stage 1 I assume she is at least in the early stages regardless of the tool being used. What is it that you are hoping they would help her with? Many with dementia have anosognosia. This is the inability to recognize their symptoms or limitations. It can be very difficult! My mom never seen a geriatric psychologist, but I would think they would be helpful. Has your mom seen a lawyer yet? This was one of the first things mom’s doctor recommended. A DPOA is very important. Don’t wait. I would also recommend you learn all you can about dementia. I have attended a great article. This site is a great resource for information, questions or just to vent. Sorry I have no insights on a geriatric psychologist.
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My husband saw a Neuro Psychologist at the VA for testing before diagnosis. Later his Neurologist referred him to a Geriatric Psychiatrist who managed his anti-psychotic medications for anxiety, agitation and aggression. I can’t see how a Geriatric Psychologist would have been of help but it may be worth a couple of visits to see for your Mom. I would speak to him/her before the appointment and see what the appointments would entail and what outcome they hoped for. I found that counseling didn’t help my husband because he didn’t understand the purpose and didn’t remember the meetings and suggestions they gave. A Psychologist might help you cope as a caregiver though if they are familiar with dementia. 💜
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I'm referring to someone that can help you prepare what's to come, how to be a caregiver and coping with it. My friend told me about that kind of psychologist. To learn all about the disease and what to expect and helping you cope. As for the stage, my mom was told that she is in stage 1. She is still independent. She can drive, dress herself, cook and stuff like that.I'm trying to get prepared for what's to come and how i deal with it. Thanks for all your answers and help!
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@malibu2155
Oh, for you?
I don't know that I've ever heard of a geriatric psychologist for this sort of thing. Generally, they're the ones doing the neuropsychological exams for PWD as part of the diagnostic process or to establish competency related to guardianship/conservatorship.
It sounds like you are seeking a therapist of some sort— a psychologist, therapist or counseling social worker most likely. If your mom was seen at a large neurology practice or memory center, they may have people on their staff who could help you or refer you to someone in the area who focuses on this kind of counseling. If you have an EPA at work they might have a list of such people, your PCP or a local support group might as well. You can always come here and ask as well. TBH, I got more help in growing as a caregiver here than anywhere.
You didn't mention it, but it's a unity horse here so I will. The driving thing is tricky. If she's in the earliest stages, she might be competent to drive at the moment. Do you drive with her regularly? Have you looked over her car and seen dings and dents? Have you contacted her insurance agent to be certain her policy is effective with an Alzheimer's diagnosis in her medical record. Dad's policy was voided upon diagnosis which is pretty common.
HB1 -
I think it is very smart of you to try and learn all you can. There are techniques and strategies that that may be helpful as things progress. For example therapeutic fibs, never ever argue or try to reason with them (after a certain point). Knowing to keep a close eye on finances in the beginning( this is often one of the first skills to go). Learning about anosognosia and conflaborations. This is their mind kind of filling in the blanks. It can come across as a lie or a tall tale. When do you take the car away(the chances of her willingly saying I shouldn’t be driving anymore are slim). How do you know? You might want to check insurance. I have read here that some insurance companies will not cover claim if there is a dementia diagnosis. What is her financial situation, learning about Medicaid may also be helpful (it’s complicated). Unfortunately I think doctors are probably not going to be much help in respect to educating you or her. Where my mom had her testing done they did offer a 2 hour evening presentation about dementia (not very helpful). I also went to a three day workshop offered by a local church that was great. This site offers links to workshops. But to be honest I have found my best resource to be this site and YouTube. Tam Cummings,Teepa Snow and Natali Edmonds. Everyone with dementia is just a bit different. So information on how your mom specifically will progress is not possible. Even the time frame is tough to determine. My mom has vascular dementia with average life expectancy of 5 years. People here have talked about a lo on year 20 of vascular dementia. Some with dementia tend to get angry and have anxiety, others get depressed and still others seem obliviously unaware of what is happening. My mil would tell us how she just got back from getting groceries (she didn’t, she was in Al) while my mom is angry and mad because she is perfectly capable of doing things for herself (she is not). I find the not knowing what’s next extremely difficult.
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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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