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....may not be true tomorrow. A lesson I'm learning.

Took out to get her hair colored/cut/styled last night, then we had a

burger at BK where Casey (my 17YO daughter) works, then took her to KMart to

pick out a birthday card for my sister. She really enjoyed getting out

again, but insisted that, now she's doing so much better, she will soon be

taking over her own affairs - wants her wallet, her address book, etc...said

she won't be living at King's permanently, etc...and if she has to then she

might as well die.

Of course, in the next sentence, she was asking where she lived because she

couldn't remember, didn't remember much of anything in fact. And when we

got back to King's after our 3-hour outing, she gave everybody hugs and

said, " It's good to be home, I missed you all so much! "

A couple of times she mentioned that she has nothing to live for - something

I haven't heard in nearly 2 weeks - but other than the memory stuff, she is

exactly like the mom I've known my whole life. Personality, mannerisms,

comments, opinions, expressions, etc. If it weren't for the memory issues

(which she covers for REALLY well most of the time!), one would never know

that she has any problems at all.

This is a 2-sided coin. On the one side, it is a happy thing that she's

doing to fantastically well. On the other, she's almost doing too well to

be in a nursing home most of the time, and she knows it. There isn't

another option at this point, other than to make her life as " normal " as

possible (with activities and outings and surrounded by her things and

enabling her to continue her habits). She knows that she has LBD but we

don't discuss it often as she's a head-in-the-sand type person; if she

weren't, she'd understand (maybe) why she's there. She does have issues

with sundowning that actually lasts into the morning also...and still

delusional but not as much as before. Hasn't mentioned hallucinations in

maybe a week or so...meds are working great, she's better than she's been in

several years...

Anyway, this is almost harder to live with (for her, I mean) than when she

was in her happy confusion, even though it should be - I would think - a

time to enjoy everything she can while she can. She can't because she's

trying to hard to get control of her life back again. (Remember, this is a

woman who never let her daughters know ANYTHING personal about her, her

business or finances or anything, and has kept us at arm's length for

years...control issues aren't anything new by any means!)

Hard to make sense of it all, for me...day by day I make decisions and try

to do the right things based on THAT day's criteria because yesterday's

doesn't necessarily still apply. So here's hoping that, today, she will

once again be satisfied with her life, and happy to have visitors and go for

rides and things, as she was for the last week or so...

His,

Sherry

www.owly.net

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---

Hi Sherry,

You are exactly right, this disease changes our los sometimes on

a daily basis and the only thing to expect is the

unexpected.Heartfelt best to you and your family Ron

In LBDcaregivers , " Sherry UpNorth "

wrote:

>

> ...may not be true tomorrow. A lesson I'm learning.

>

> Took out to get her hair colored/cut/styled last night, then

we had a

> burger at BK where Casey (my 17YO daughter) works, then took her

to KMart to

> pick out a birthday card for my sister. She really enjoyed

getting out

> again, but insisted that, now she's doing so much better, she will

soon be

> taking over her own affairs - wants her wallet, her address book,

etc...said

> she won't be living at King's permanently, etc...and if she has to

then she

> might as well die.

>

> Of course, in the next sentence, she was asking where she lived

because she

> couldn't remember, didn't remember much of anything in fact. And

when we

> got back to King's after our 3-hour outing, she gave everybody

hugs and

> said, " It's good to be home, I missed you all so much! "

>

> A couple of times she mentioned that she has nothing to live for -

something

> I haven't heard in nearly 2 weeks - but other than the memory

stuff, she is

> exactly like the mom I've known my whole life. Personality,

mannerisms,

> comments, opinions, expressions, etc. If it weren't for the

memory issues

> (which she covers for REALLY well most of the time!), one would

never know

> that she has any problems at all.

>

> This is a 2-sided coin. On the one side, it is a happy thing that

she's

> doing to fantastically well. On the other, she's almost doing too

well to

> be in a nursing home most of the time, and she knows it. There

isn't

> another option at this point, other than to make her life

as " normal " as

> possible (with activities and outings and surrounded by her things

and

> enabling her to continue her habits). She knows that she has LBD

but we

> don't discuss it often as she's a head-in-the-sand type person; if

she

> weren't, she'd understand (maybe) why she's there. She does have

issues

> with sundowning that actually lasts into the morning also...and

still

> delusional but not as much as before. Hasn't mentioned

hallucinations in

> maybe a week or so...meds are working great, she's better than

she's been in

> several years...

>

> Anyway, this is almost harder to live with (for her, I mean) than

when she

> was in her happy confusion, even though it should be - I would

think - a

> time to enjoy everything she can while she can. She can't because

she's

> trying to hard to get control of her life back again. (Remember,

this is a

> woman who never let her daughters know ANYTHING personal about

her, her

> business or finances or anything, and has kept us at arm's length

for

> years...control issues aren't anything new by any means!)

>

> Hard to make sense of it all, for me...day by day I make decisions

and try

> to do the right things based on THAT day's criteria because

yesterday's

> doesn't necessarily still apply. So here's hoping that, today,

she will

> once again be satisfied with her life, and happy to have visitors

and go for

> rides and things, as she was for the last week or so...

>

> His,

> Sherry

> www.owly.net

>

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