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Patti:

Welcome. I'm so glad you're joining us. I know you'll find this

site extremely supportive and very warm. Those of us who visit

regularly can't imagine not checking in or connecting with this group.

The info. you provided re: the Alzheimer's Association will be very

valuable to those who still are caring for their LOs at home.

Unfortuantely, my dad has been in a nh since January (it still hurts

to think of him there) since my mom, who would have been his primary

caregiver, is also ill and couldn't care for him on her own. I do

know that several members will appreciate the info. though.

Anyhow Patti, welcome again. Hope to " see " you here often.

All good things,

Abby

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Welcome Patti

This is a group you will want to keep in touch with. They are like a

lifeline to caregivers.

Kath

Patti

> Patti:

>

> Welcome. I'm so glad you're joining us. I know you'll find this

> site extremely supportive and very warm. Those of us who visit

> regularly can't imagine not checking in or connecting with this group.

>

> The info. you provided re: the Alzheimer's Association will be very

> valuable to those who still are caring for their LOs at home.

> Unfortuantely, my dad has been in a nh since January (it still hurts

> to think of him there) since my mom, who would have been his primary

> caregiver, is also ill and couldn't care for him on her own. I do

> know that several members will appreciate the info. though.

>

> Anyhow Patti, welcome again. Hope to " see " you here often.

>

> All good things,

>

> Abby

>

>

>

>

>

>

> Welcome to LBDcaregivers.

>

>

>

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  • 1 month later...
Guest guest

Hello Abby,

Nice to meet you. I am 55 and was diagnosed last week with Diffuse

Lewy Body Disease. I was ffinally told after 7 years of seeing my

Neurologist that I had PD In 1996. It was before my Dad died with PD.

Thank you for taking the time to read what I write. I hadn't thought

at first when I joined that you all would have questions of me and

would be interested so it has really made me feel welcome in thinking

I do have something to offer back to you....Hugs....Patti

> Hello:

>

> I just had to say hello. I've search back for your first post and

> haven't been able to locate it. Am I right in assuming you've been

> diagnosed with LBD or a dementia of some sort?

>

> My name is Abby and my dad was diagnosed with LBD October of 2003.

> He also has a brain tumour and some pretty debilitating Parkinson's

> symptoms. Nevertheless, he is having a good time now and we're

> grateful for having him with us.

>

> I've been a part of this group since my dad was diagnosed and it

has

> been a godsend. I hope this group brings you just as much as it

has

> to me but if you're half as lucky you're still in a good spot.

>

> Welcome to this board. I can tell people really appreciate your

> input.

>

> Abby

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Guest guest

Patti,just wanted to introduce myself, i'm .

I'm in Glasgow,Scotland and i joined the group in January 2003 when my granda

Bert was coming into the last stages of the disease(he passed on 16th August

2003).

I'm so glad you've joined the group, you sound like one amazing lady and i look

forward to getting to know you.

Love .x

Re: Patti

Hello Abby,

Nice to meet you. I am 55 and was diagnosed last week with Diffuse

Lewy Body Disease. I was ffinally told after 7 years of seeing my

Neurologist that I had PD In 1996. It was before my Dad died with PD.

Thank you for taking the time to read what I write. I hadn't thought

at first when I joined that you all would have questions of me and

would be interested so it has really made me feel welcome in thinking

I do have something to offer back to you....Hugs....Patti

> Hello:

>

> I just had to say hello. I've search back for your first post and

> haven't been able to locate it. Am I right in assuming you've been

> diagnosed with LBD or a dementia of some sort?

>

> My name is Abby and my dad was diagnosed with LBD October of 2003.

> He also has a brain tumour and some pretty debilitating Parkinson's

> symptoms. Nevertheless, he is having a good time now and we're

> grateful for having him with us.

>

> I've been a part of this group since my dad was diagnosed and it

has

> been a godsend. I hope this group brings you just as much as it

has

> to me but if you're half as lucky you're still in a good spot.

>

> Welcome to this board. I can tell people really appreciate your

> input.

>

> Abby

Welcome to LBDcaregivers.

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Guest guest

I am very Pleased to make your aquaintance . I hope we can get

to know one another as well. Oooooh If I could make one last request

in life it would be to visit England, Ireland, Scotland and even

Wales. It is the area of my heritage. That is my dream and I am not

giving it up. Thank you so much for responding and very happy to see

you here.....Hugs.....Patti

> > Hello:

> >

> > I just had to say hello. I've search back for your first post

and

> > haven't been able to locate it. Am I right in assuming you've

been

> > diagnosed with LBD or a dementia of some sort?

> >

> > My name is Abby and my dad was diagnosed with LBD October of

2003.

> > He also has a brain tumour and some pretty debilitating

Parkinson's

> > symptoms. Nevertheless, he is having a good time now and we're

> > grateful for having him with us.

> >

> > I've been a part of this group since my dad was diagnosed and

it

> has

> > been a godsend. I hope this group brings you just as much as

it

> has

> > to me but if you're half as lucky you're still in a good spot.

> >

> > Welcome to this board. I can tell people really appreciate

your

> > input.

> >

> > Abby

>

>

>

> Welcome to LBDcaregivers.

>

>

>

>

>

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Guest guest

Hmm Patti, let me think about how we can maybe bring a piece of Scotland to you,

i'll get back to you on that one.

.x

Re: Patti

I am very Pleased to make your aquaintance . I hope we can get

to know one another as well. Oooooh If I could make one last request

icen life it would be to visit England, Ireland, Scotland and even

Wales. It is the area of my heritage. That is my dream and I am not

giving it up. Thank you so much for responding and very happy to see

you here.....Hugs.....Patti

> > Hello:

> >

> > I just had to say hello. I've search back for your first post

and

> > haven't been able to locate it. Am I right in assuming you've

been

> > diagnosed with LBD or a dementia of some sort?

> >

> > My name is Abby and my dad was diagnosed with LBD October of

2003.

> > He also has a brain tumour and some pretty debilitating

Parkinson's

> > symptoms. Nevertheless, he is having a good time now and we're

> > grateful for having him with us.

> >

> > I've been a part of this group since my dad was diagnosed and

it

> has

> > been a godsend. I hope this group brings you just as much as

it

> has

> > to me but if you're half as lucky you're still in a good spot.

> >

> > Welcome to this board. I can tell people really appreciate

your

> > input.

> >

> > Abby

>

>

>

> Welcome to LBDcaregivers.

>

>

>

>

>

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Guest guest

Abby,

I must agree with you. They are friends though we would not have met

otherwise and withthe internet it opens up a whole new line of ways

of meeting people you would never get to know. Each in their own way

offers a richness to our lives. I believe we can only be better

humans for meeting them and sharing in our happy times as well as sad

ones. Each day is a miracle in itself. I am certainly greatful I have

met each of you and I hope you all will enjoy sharing with me just

what you have been through for it settles in my mind some ideas I

have about the brains function itself. It also provides a loving a

caring atmosphere to communicate my fearsand experiences to you. I

feel comfortable here and that makes it easy for me to open up. I

only wished that more people who are going through this first hand

would join in as well and maybe I can somehow set an example to let

them know it is ok to talk about this and to not be ashamed as it is

not their fault. Communication leads to knowledge and knowledge will

lead to better treatment and cure.....Hugs....Patti

> Patti:

>

> Seeing new names on the board is such a mixed blessing. We're

happy

> people found us and want others to have the help and understanding

> we've all found on here but we're sad that there is a need for us

to

> meet here in the first place. We wish we could meet under

different

> circumstances.

>

> I applaud your courage for joining and being willing to educate. I

> look forward to speaking to you often on this board.

>

> Abby

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Guest guest

" Communication leads to knowledge and knowledge will

lead to better treatment and cure..... "

Patti-

I greatly admire what you write, and how you say it. Thank you

for being here, and allowing me insight to Lewy Body itself.

Hugs from Des Moines-

Sandie

-- " Patti " wrote:

Abby,

I must agree with you. They are friends though we would not have met

otherwise and withthe internet it opens up a whole new line of ways

of meeting people you would never get to know. Each in their own way

offers a richness to our lives. I believe we can only be better

humans for meeting them and sharing in our happy times as well as sad

ones. Each day is a miracle in itself. I am certainly greatful I have

met each of you and I hope you all will enjoy sharing with me just

what you have been through for it settles in my mind some ideas I

have about the brains function itself. It also provides a loving a

caring atmosphere to communicate my fearsand experiences to you. I

feel comfortable here and that makes it easy for me to open up. I

only wished that more people who are going through this first hand

would join in as well and maybe I can somehow set an example to let

them know it is ok to talk about this and to not be ashamed as it is

not their fault. Communication leads to knowledge and knowledge will

lead to better treatment and cure.....Hugs....Patti

> Patti:

>

> Seeing new names on the board is such a mixed blessing. We're

happy

> people found us and want others to have the help and understanding

> we've all found on here but we're sad that there is a need for us

to

> meet here in the first place. We wish we could meet under

different

> circumstances.

>

> I applaud your courage for joining and being willing to educate. I

> look forward to speaking to you often on this board.

>

> Abby

Welcome to LBDcaregivers.

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Guest guest

I agree with you wholeheartedly. Communication is the key insofar as

illnesses such as this are concerned. I long for the day when I can

tell someone my dad has Lewey Body Dementia and not have them look at

me as if I've suddenly sprouted thirteen really unattractive heads.

The only way to be successful in this regard is via us getting out

there and you, who are actually living the cause, are our very best

resource.

I will certainly be willing to share my fears with you although, be

forewarned, they tend to be many although, since my father is doing

somewhat better, I'll be happy to share my good times with you as

well so it won't be all doom and gloom.

Good to know you are enjoying your life. I assure you, your

participation on this site is incredible and so very welcome.

Abby

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