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Randomthought

(882 posts)
Wed Aug 14, 2024, 04:31 AM Aug 14

Is there support groups for spouses of dementia patients

We don't have a definitive diagnosis yet, but the neurologist who saw my husband today said "there is something going on".
I have been dealing with this issue for a few years. He gets scammed by phone and email scams, 30 grand lost over the last 5 years.
I have taken over our finances as much as I can. When I have to leave the house, I put his phone on do not disturb and make him promise to stay off the computer

I'm a strong woman but sometimes a little support would help.

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Is there support groups for spouses of dementia patients (Original Post) Randomthought Aug 14 OP
There is an Elder Caregivers forum. SleeplessinSoCal Aug 14 #1
TY Randomthought Aug 14 #2
Sounds to me like you have a good grasp on reality. SleeplessinSoCal Aug 14 #9
Check out these guys bucolic_frolic Aug 14 #3
TY Randomthought Aug 14 #4
I understand too well. no_hypocrisy Aug 14 #5
OMG Randomthought Aug 14 #6
My Mom had Parkinson's Dementia,,,, KarenS Aug 14 #7
Contact the Alzheimer's Association Dave in VA Aug 14 #8
My husband died of vascular dementia 2+ years ago CountAllVotes Aug 23 #10

SleeplessinSoCal

(9,611 posts)
1. There is an Elder Caregivers forum.
Wed Aug 14, 2024, 04:51 AM
Aug 14

My wonderful hubby died on July 8th after living 10 years with Dementia/Alzheimer's.

I've been through what you are embarking on. It can be very hard and getting support from DU will help as there are others going through this. I never received help from the Alzheimer's Association, though I always intended to connect with them. I kept adapting to his reality.

I was pretty honest with him up until he had only weeks to live. I couldn't tell him he was dying. He was always so happy to just be home with me. And as I prepared myself psychologically, I just kept telling him how much I loved him. Tonight I've been missing him terribly. I just can't wrap my head around the fact that he's gone.

Please know how adapting to the oddities that may emerge could be your best course of action. All people react differently. There is no absolute pattern. But adapting to the changes will keep you two close. Just remember that Love is the answer.

Randomthought

(882 posts)
2. TY
Wed Aug 14, 2024, 05:00 AM
Aug 14

Thank you so much. I had already decided that I will always treat him with respect no matter what.
Frankly, I am scared. Scared for our future, scared for his health, and scared that I will not be strong enough.

SleeplessinSoCal

(9,611 posts)
9. Sounds to me like you have a good grasp on reality.
Wed Aug 14, 2024, 01:41 PM
Aug 14

I found that the process makes you stronger. Hopefully you get help when you need it from family and friends. Once you get confirmation that he is on the Dementia Spectrum, you can seek help and advice from your doctor and the Alzheimer's Association.

David was too old for most of the study programs. But we did participate in one testing a pill to cure Alzheimer's. Turned out the medication wasn't helpful. But that process was a course of action that we did that was proactively taking on Dementia. The study taught me a lot. And there have been successful studies that you may benefit from.

His GP put him on Namenda and Donepezil early on. And he was advised to receive cognitive therapy. Through that we found a geriatric physician who did studies on treatment. We saw him for 9 years. He was the expert we needed.

One thing I recall reading was how to be empathetic to the oddities that may emerge. One suggestion was to try to get dressed with gloves on. It helps to put yourself in his place. When it finally occured and I needed to help David get dressed, I was ready. But there were so many odd things going on. You learn about visual spacial problems and how it manifests.

I hope these things help you prepare for the future. There have been advances in treatment. I hope that you and your husband can benefit from them. And from others like me who completely understand and want to help.

bucolic_frolic

(46,561 posts)
3. Check out these guys
Wed Aug 14, 2024, 05:25 AM
Aug 14
https://www.alz.org/

Spend a few minutes perusing their site, then give them a call. Their counselors knew quite a lot about everything.

no_hypocrisy

(48,555 posts)
5. I understand too well.
Wed Aug 14, 2024, 05:33 AM
Aug 14

My father had undiagnosed dementia.

He'd get phone calls from solicitors and thought they knew him b/c they called him by his first name and sounded so friendly. I nearly hit the roof when he gave out his Social Security number. Or drove alone from NYC to NJ after cataract surgery with one eye bandaged and the other with another cataract.

Take care of yourself or you'll get caregivers' burnout.



Randomthought

(882 posts)
6. OMG
Wed Aug 14, 2024, 05:40 AM
Aug 14

You must almost had a stroke.
I took care of father many years ago so I am familiar with burnout.
Difference my father was a nasty ass but my husband is the kindest sweetest person ever.

KarenS

(4,592 posts)
7. My Mom had Parkinson's Dementia,,,,
Wed Aug 14, 2024, 06:12 AM
Aug 14

Here in Mesa AZ a suburb of the Phoenix Metro area, they had Support groups for the caregivers and also some "Day Care for Adults" programs so that caregivers could have some time for themselves. My Dad couldn't/wouldn't take advantage of these things.

If you have any residential Senior Homes around, they may have some resources for you.

Sending ((Hugs))

Dave in VA

(2,181 posts)
8. Contact the Alzheimer's Association
Wed Aug 14, 2024, 06:36 AM
Aug 14

alz.org

We have cared for both of our mothers who had dementia. They were a tremendous help.

One of the first rules for caring for someone is that you are no good to them if you are not caring for yourself.

Please contact them ASAP!

CountAllVotes

(21,032 posts)
10. My husband died of vascular dementia 2+ years ago
Fri Aug 23, 2024, 09:35 PM
Aug 23

Its been a lonely road to be on, I know that much.

There was no "help" until the very end at $500.00 a day for the last stop hospice place.

He'd broken his hip and failed to recover and could not breathe or swallow.

I wish I had some good advice but I don't.

I've lost so much, so very much.

Hang-in there best you can and he's lucky he's got you around.

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