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Hi, Sue,

Just wanted to say a quick welcome to the group. As many of us will say, we

are glad you found us, but sorry you need to be here. The hallucinations you

speak of with your mom are usually one of the hallmarks of LBD. I find them

to be one of the most frustrating things to deal with. I am the primary

caregiver for my 75 year old dad who lives at home. He was diagnosed in 2000 and

is

fairly far along his LBD journey. Please let us know how things are going

when you have time. and again, welcome.

Big hugs,

Piper

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Gene and Sue wrote:Hi,

I am the 52 y/o daughter of my Mom whom I believe has LBD. She is in a care

home and is nearing end stage I think. I have read about LBD and I believe

that she is a victim of this disease. What seems different from other dementia

victims is her pervasive hallucinations. She had a strong exacerbation follwing

AAA sugery over a year ago. She has not been formally diagnosed even though she

was seen by a neurologist following surgery. I am interested in reading about

the particualr issues facing LBD caregivers as opposed to caring for any other

dementia sufferer. I will check in here and there to see what issues are being

discussed.

Thanks, Sue

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Guest guest

Sue,

Welcome to the group. You won't find a better bunch of people anywhere else

in the world!

Courage

Join

>Hi,

> I am the 52 y/o daughter of my Mom whom I believe has LBD. She is in a

care home and is nearing end stage I think. I have read about LBD and I

believe that she is a victim of this disease. What seems different from

other dementia victims is her pervasive hallucinations. She had a strong

exacerbation follwing AAA sugery over a year ago. She has not been formally

diagnosed even though she was seen by a neurologist following surgery. I am

interested in reading about the particualr issues facing LBD caregivers as

opposed to caring for any other dementia sufferer. I will check in here and

there to see what issues are being discussed.

>Thanks, Sue

>

>

>

>

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Guest guest

Hi Sue,

It is my understanding that LBD is not diagnosed because many doctors are

not aware of how it differs from Alzheimers.

My mother use to have hallucinations but she was never frightened of them.

They were just part of her life.

M

>

>Reply-To: LBDcaregivers

>To: LBDcaregivers

>Subject: Join

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>

>Hi,

> I am the 52 y/o daughter of my Mom whom I believe has LBD. She is in a

>care home and is nearing end stage I think. I have read about LBD and I

>believe that she is a victim of this disease. What seems different from

>other dementia victims is her pervasive hallucinations. She had a strong

>exacerbation follwing AAA sugery over a year ago. She has not been

>formally diagnosed even though she was seen by a neurologist following

>surgery. I am interested in reading about the particualr issues facing LBD

>caregivers as opposed to caring for any other dementia sufferer. I will

>check in here and there to see what issues are being discussed.

>Thanks, Sue

>

>

>

>

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