Anonymous wrote:Anonymous wrote:Ok a few things. She sounds like she is doing a lot. Working, grieving, child living at home, hosting large family gatherings, etc. She also may have some hearing loss and just general getting older issues.
With my mom there were alarming signs like getting lost trying to drive home from church which she had done for 40+ years. Finding her phone in the fridge. Those sorts of things which were eye opening.
She put her dentures in the China cabinet during Christmas two years ago. She took them out and was putting away something and we couldn’t find them for weeks. She called me crying because my dad said she’s always forgetting things and said if she has dementia to put her in a home. I just thought that was absentmindedly putting them in wrong place so I wasn’t worried and told her that.
Anonymous wrote:Wow!
First of all 69 is not old.
There are certain things I forget frequently.
Everyone has their ‘thing’
And yea it is easy to ignore the beeping, it becomes white noise.
There’s garage near my office that has a makes a constant noise and it has become white noise to me, I’m barely conscious of it.
I’m still amazed you think 69 is really old.
Anonymous wrote:My mom is 69. Cognitively she’s okay but I’ve noticed it’s been declining but again, she’s 69 so I figure that’s normal. We were talking about the entire family (22 of us) having Thanksgiving at the beach house last year and she said, “we didn’t have Thanksgiving there”. My brother and I looked at her confused and told her that we did but she said again that we hadn’t. We then recounted stories of things that we did and then that’s when she remembered. Outside of that incident there’s been nothing truly alarming, just general forgetfulness due to old age I guess - she’ll occasionally repeat something she just told me the day prior. Other times she’s repeating word for word what she heard on the news and things she’s read when debating politics (she loves politics), and this is what gives me some reassurance.
My mother teaches virtually and everyday during the work week she has coffee. A handful of those days she forgets her coffee in the microwave despite it beeping non stop for hours, which I can hear from upstairs. I attributed this to her not hearing the beeping because she’s obviously teaching. However, this happens so frequently that it’s causing me to be worried. So I don’t know if I’m overreacting here or not.
Thoughts?
Anonymous wrote:Anonymous wrote:Anonymous wrote:Anonymous wrote:Very little a doctor can do. Current meds make little or no difference.
That’s not true.There are medications that treat symptoms of most dementias other than vascular and FTD. There is a new medication that slows progression https://www.alz.org/alzheimers-dementia/treatments/lecanemab-leqembi already approved, and LLY has two more getting close to approval that are probably going to be even better.
And there are lifestyle interventions that can be very helpful as well. Nevertheless, OP just needs to focus on what (if anything) is going on. Then her family can deal with facts.
The new medication lecanemab is $26,000 a year, the benefits are minimal and might not even be clinically significant in women at all. There is also a risk of brain bleeds and there is concerned about other side effects including brain shrinkage that scientist really aren't sure what the long term effects will be.
One of the test used in the study is the Clinical Dementia Rating Scale which assesses cognitive and functional performance in six areas: memory, orientation, judgment and problem solving, community affairs, home and hobbies, and personal care. Scores range from 0 meaning no dementia to 18 meaning the most significant dementia. Low scores are better. Over the clinical trial the Mean change of CDR-SB from baseline at 18 months was 1.21 for the lecanemab group and 1.66 for the placebo groups. Both groups declined and the decline among both groups was much larger than the difference between the groups. The difference wasn't even half a point.
0 = no dementia/normal
0.5 – 4.0 = questionable
0.5 – 2.0 = questionable impairment
2.5 – 4.0 = very mild dementia
4.5 – 9.0 = mild dementia
9.5 – 15.5 = moderate dementia
16.0 – 18.0 = severe dementia
Is that worth not just $26,000 a year but the time caregivers are going to have to dedicate to take their loved one every other week for an infusion the takes an hour. So the caregiver has to pick up their loved one if they aren't living with them and make sure they are ready/help them get ready, drive over to where they can get the infusion, check in and have the elderly patient check in, get the one hour infusion and drive back. All that can take half a day. There are cheaper generic pills that are almost as good. And good is relative because there really aren't any good treatments.
The other issue is that for all of this minimal improvement the person with dementia/alzheimers might have their lives extended. In one study about a dementia drug called donzepil those taking the drug lived about 2 1/2 years longer than people not on the medication. I absolutely do not want to live 2 1/2 years longer if I had dementia and as a caretaker for my mother who has dementia- I don't want her to suffer for 2 1/2 more years and I certainly do not want the stress of caregiving to last 2 1/2 years longer.
You are cherry picking and not current . It’ is covered by medicaid and Medicare. It slows progression by 26% and multiple better drugs are nearing approval. There are lifestyle interventions. But this is a derailment. The point is for OP or others in her situation, don’t panic, seek competent evaluations and proceed from there.
Anonymous wrote:Anonymous wrote:Anonymous wrote:Very little a doctor can do. Current meds make little or no difference.
That’s not true.There are medications that treat symptoms of most dementias other than vascular and FTD. There is a new medication that slows progression https://www.alz.org/alzheimers-dementia/treatments/lecanemab-leqembi already approved, and LLY has two more getting close to approval that are probably going to be even better.
And there are lifestyle interventions that can be very helpful as well. Nevertheless, OP just needs to focus on what (if anything) is going on. Then her family can deal with facts.
The new medication lecanemab is $26,000 a year, the benefits are minimal and might not even be clinically significant in women at all. There is also a risk of brain bleeds and there is concerned about other side effects including brain shrinkage that scientist really aren't sure what the long term effects will be.
One of the test used in the study is the Clinical Dementia Rating Scale which assesses cognitive and functional performance in six areas: memory, orientation, judgment and problem solving, community affairs, home and hobbies, and personal care. Scores range from 0 meaning no dementia to 18 meaning the most significant dementia. Low scores are better. Over the clinical trial the Mean change of CDR-SB from baseline at 18 months was 1.21 for the lecanemab group and 1.66 for the placebo groups. Both groups declined and the decline among both groups was much larger than the difference between the groups. The difference wasn't even half a point.
0 = no dementia/normal
0.5 – 4.0 = questionable
0.5 – 2.0 = questionable impairment
2.5 – 4.0 = very mild dementia
4.5 – 9.0 = mild dementia
9.5 – 15.5 = moderate dementia
16.0 – 18.0 = severe dementia
Is that worth not just $26,000 a year but the time caregivers are going to have to dedicate to take their loved one every other week for an infusion the takes an hour. So the caregiver has to pick up their loved one if they aren't living with them and make sure they are ready/help them get ready, drive over to where they can get the infusion, check in and have the elderly patient check in, get the one hour infusion and drive back. All that can take half a day. There are cheaper generic pills that are almost as good. And good is relative because there really aren't any good treatments.
The other issue is that for all of this minimal improvement the person with dementia/alzheimers might have their lives extended. In one study about a dementia drug called donzepil those taking the drug lived about 2 1/2 years longer than people not on the medication. I absolutely do not want to live 2 1/2 years longer if I had dementia and as a caretaker for my mother who has dementia- I don't want her to suffer for 2 1/2 more years and I certainly do not want the stress of caregiving to last 2 1/2 years longer.
Anonymous wrote:And sometimes I do forget the cup in the microwave if I'm busy doing other things, but our microwave stops beeping after a certain point.
Anonymous wrote:Anonymous wrote:The takeaway for me from this thread is that people reheat their coffee in the microwave.
I have never done that, never thought to do so, and I am slightly grossed out to hear people do that.
I do this every day, multiple times, with coffee and hot tea. I like hot beverages hot versus lukewarm or room temperature, and I don't finish the cup before it cools.
Anonymous wrote:The takeaway for me from this thread is that people reheat their coffee in the microwave.
I have never done that, never thought to do so, and I am slightly grossed out to hear people do that.