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Dear Lucy:

Welcome to this site. We are here to give you support and information.

Please tell us about your loved one with LBD, the symtoms that are present and

how

you are coping. I will add you and your family to my LBD prayers, God bless

you, hugs,

Josie

Miami, Florida, U.S.A.

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Hi Josie,

thanks to contact me. I AM REAL and I am from Italy, so

sometimes I have some probles of language, expecially when

you write down abbreviations like pg, mi etc. Anyhow I am

sure you can help me on the run!

Unfortunately I am here for bad problems in my family: my

Mom (77 in May) has LBD, very hardly diagnosticated late

last year. At the moment she can not speak, not walk, not

eat alone and sleeps almost all the time. I really really

sad, as you can imagine as I live far from her and I miss

a lot her voice by phone. In the past decade there wre

only some ciao and simplest sentence but now she has

fallen in silence that probably is out of code in this

illness. Can you help me in explaining? Can I do

something?

I miss my Mom a lot.

All my love

Lucy

On Wed, 31 Mar 2004 08:29:17 EST

regattabh@... wrote:

Luciana Mirenghi

Luciana Mirenghi

Luciana Mirenghi

Luciana Mirenghi

Luciana MirenghiDear Lucy:

Luciana Mirenghi

Luciana MirenghiWelcome to this site. & nbsp; We are here to

Luciana Mirenghigive you support and information. & nbsp;

Luciana MirenghiPlease tell us about your loved one with

Luciana MirenghiLBD, the symtoms that are present and how

Luciana Mirenghiyou are coping. & nbsp; I will add you and

Luciana Mirenghiyour family to my LBD prayers, God bless

Luciana Mirenghiyou, hugs,

Luciana Mirenghi

Luciana MirenghiJosie

Luciana MirenghiMiami, Florida, U.S.A.

Luciana Mirenghi

Luciana Mirenghi

Luciana Mirenghi[Non-text portions of this message have

Luciana Mirenghibeen removed]

Luciana Mirenghi

Luciana Mirenghi

Luciana Mirenghi

Luciana Mirenghi

Luciana Mirenghi

Luciana MirenghiWelcome to LBDcaregivers. & nbsp; & nbsp;

Luciana Mirenghi

Luciana Mirenghi

Luciana Mirenghi

Luciana Mirenghi

Luciana Mirenghi

Luciana Mirenghi

Luciana Mirenghi

Luciana Mirenghi

Luciana Mirenghi

Luciana Mirenghi

Luciana Mirenghi

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Guest guest

Welcome Lucy,

Sorry that you and your family have been stricken by this disease.

M

>

>Reply-To: LBDcaregivers

>To: LBDcaregivers

>Subject: new subscription

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>Hello everybody and nice to join you.

>All the best

>Lucy (italy)

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Dear Lucy:

I think they can hear and understand everything. My father was physically

very well, he tried to speak to us, but the words would not come. He became

very, very frustrated. If we tried to guess, we were usually wrong because he

wanted to talk about something else than what was happening. He got angry with

himself. I feel like it is the mind trapped inside the body. They do reason

when they are not having a dementia attack. Ironically, when they are having

dementia, they can talk and insult everyone.

I think they can reason, not in an elementary way, but as their mature

selves. sometimes the DRs say that to make the family feel better and to hide

the

fact that they cannot do anything about it. You can do something. You and

your family can talk to your mom as always. You can tell her what is happening

in your lives outside of the hospital. You can tell her about your hopes and

dreams and make her feel that your lives will go on and now you can take care

of things. Tell her you love her on the phone. She may be wondering where you

are. Have someone put the phone to her and you say hello and tell her about

your life.

I send you my support. Love,

Josie

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Josie,

thanks for the message. I can write to all of you,

meanwhile working. It is not nice, but the only way to

communicate with you.

I decided to join the group as I felt this kind of illness

frighten too much and I was starting to feel rather alone,

with a bigget " hole " since three weeks ago when Mom

stopped speaking at the phone. I am living far from her,

and my original family as I work and I am married here 100

km far. So the phone was very important to " feel " her. I

can hardly believe that she cannot say a " yes " or a sound

anymore. I am sure she can ear, in fact at first I was

speaking with her without any answer, but maybe it was

helping only myself to " denie " what was happening.

Now I am aware she is quickly going down. Since last year,

she has lot a lot and bocomed passive at all.

How much does it last? I have an older sister and we both

are asking if she suffers inside eventhough we can not see

any sigh on her face.

The doctor says she forgets as easily she can feels

elementary things. But I am not sure. The last time I was

to her when I told her I was going with my familiy she

started to cry in a strange way. It was really breaking my

heart as this confirms that all LBD people can feel

exactly as we do. Probably there is, in some cases, no

strenght to speach or to move eyes and face. But I believe

they all can feel and not in a elementary way. What's your

opinion?

Love to you and everybody

Lucy

On Wed, 31 Mar 2004 08:29:17 EST

regattabh@... wrote:

Luciana Mirenghi

Luciana Mirenghi

Luciana Mirenghi

Luciana Mirenghi

Luciana MirenghiDear Lucy:

Luciana Mirenghi

Luciana MirenghiWelcome to this site. & nbsp; We are here to

Luciana Mirenghigive you support and information. & nbsp;

Luciana MirenghiPlease tell us about your loved one with

Luciana MirenghiLBD, the symtoms that are present and how

Luciana Mirenghiyou are coping. & nbsp; I will add you and

Luciana Mirenghiyour family to my LBD prayers, God bless

Luciana Mirenghiyou, hugs,

Luciana Mirenghi

Luciana MirenghiJosie

Luciana MirenghiMiami, Florida, U.S.A.

Luciana Mirenghi

Luciana Mirenghi

Luciana Mirenghi[Non-text portions of this message have

Luciana Mirenghibeen removed]

Luciana Mirenghi

Luciana Mirenghi

Luciana Mirenghi

Luciana Mirenghi

Luciana Mirenghi

Luciana MirenghiWelcome to LBDcaregivers. & nbsp; & nbsp;

Luciana Mirenghi

Luciana Mirenghi

Luciana Mirenghi

Luciana Mirenghi

Luciana Mirenghi

Luciana Mirenghi

Luciana Mirenghi

Luciana Mirenghi

Luciana Mirenghi

Luciana Mirenghi

Luciana Mirenghi

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Guest guest

Dear Lucy

I am glad you 'found' this group. This terrible disease can make you feel

very isolated and depressed. That's why we're here - to give you the support

you need.

You ask if LBD sufferers have deep feelings and recognise what is happening

to them? My answer is 'yes' - sadly they do know and can feel very afraid

and depressed.

My dad died 21st Oct 2002. He was 67 years of age. I think he had LBD for

about 7-9 years overall, but had it much worse in the final 2 years. He

would get VERY distressed about the way he looked, what he couldn't do, how

he felt. He knew that something was terribly wrong even though he couldn't

explain it. He would get paranoid, extremely fearful and very depressed.

Unlike dementia such as Alzheimer's - there is no escape. LBD patients don't

retreat into make-believe, fantasy world of blissful delusion. I believe

that LBD patients have a dreadful premonition of impending disaster - they

know something bad is happening and that it's out of their control. THAT'S

why proper nursing care is so critical- these poor souls need immeasurable

care, love, understanding and reassurance.

That's also why this bastard is so hard to watch as it destroys their

lives...you feel so helpless and overwhelmed!

BUT you sound like you are doing a great job. You are aware that your mum is

very sensitive and vulnerable- so you can respond with the appropriate

kindness and gentleness.

In my opinion the doctor was wrong - LBD people do NOT forget as easily as

they feel. That's rubbish! They may forget some things but my dad was

totally aware of the misery of his condition.

Maybe he said that to make you feel better?

LBD is a heartbreaker - that's the cruel truth as so many here can testify.

Sorry if that is blunt but I think you have better insight and understanding

than that doctor!

Love to you too

Sally (UK)x

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Lucy,

Please accept my warm welcome to the group although it may be a

little late. How brave you are to write in a language which is not

your own but if I must say so, you are doing a great job. Please

know that no matter how you write, the folks here somehow know what

is in the heart. Together we do what we are unable to do alone.

Hugs,

Betty

> Hello everybody and nice to join you.

> All the best

> Lucy (italy)

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