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Thank all of you for your prayers and kind thoughts and words. The

warmth of your thoughts was felt here and with my family in Denver. It

had been such a long, hard fought battle, but Dad is at peace and the

suffering is at an end. And, I am no longer the red headed step child.

I am safely at Carol's; and a safe haven at this juncture of my life

is so terribly important. My thanks to all of you.

Gail in Denver, but still in Florida

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  • 1 month later...
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Thank you , I could not remember for the life

of me what it was called. I got the first two letters

right anyway. Hopefully, you have helped someone here

today that was not aware of NPH.

I would love if just even one person here could

discover their LO(Loved One) has NPH and not LBD.

Jan Colello, California, San Francisco Bay Area

--- wrote:

> It is called NPH. Here is a link about it. A man

> at my church was recently diagnosed with it. The

> treatment has seemed to help relieve the symptoms.

>

> http://www.lifenph.com/

>

>

> Re: Just Needing to Vent

> A Little/April

>

>

>

> >

> > > Jan,

> > >

> > > My FIL was diagnosed with PD almost two years

> ago at

> > > the age of 67.

> > > We've all talked that before that time, he, of

> > > course, had some

> > > slight tremors in his hand, but he was just

> " off " ,

> > > for lack of a

> > > better description. Something just wasn't

> quite

> > > right about him.

> > > We started noticing signs of cognitive

> difficulties

> > > probably 6-8

> > > mos. prior to his diagnosis. I would say that

> 6

> > > months or so after

> > > his diagnosis, he started to take a turn for

> the

> > > worse. He began

> > > losing his mobility and had to use a cane.

> His

> > > memory started to

> > > get foggy. He would sometimes say things that

> made

> > > no sense. He,

> > > once, walked into the room rattling off about

> > > someone and what they

> > > had done recently. It didn't dawn on my MIL

> at

> > > first, but then she

> > > concluded that he was talking about someone

> they

> > > vaguely knew a long

> > > time ago in another state and hadn't kept in

> contact

> > > with. It was

> > > just so random, but he was convinced the event

> had

> > > happened a day or

> > > so ago. During this time, he was evaluated by

> a

> > > neurologist and

> > > couldn't properly identify the hands on the

> clock

> > > when asked to show

> > > a certain time. His handwriting also became

> > > dramatically worse and

> > > he grew very short-tempered. As a few more

> months

> > > went by, he began

> > > having falls. His gait become slower and he

> > > developed the blank

> > > stare on his face. He was still able to drive,

> at

> > > that point, but

> > > was having some difficulty. He lost his

> ability to

> > > do simple math

> > > problems and calculate tips. It was probably

> close

> > > to this time

> > > that he was told he might have some LBD. As

> time

> > > has marched on,

> > > particularly in the last 4-6 months, he has

> really

> > > gotten a lot

> > > worse. He lost his ability to drive about 5

> months

> > > ago because he

> > > ran into a neighbors mailbox. He'd also

> hopped into

> > > the car alone

> > > and drove off behind a church. It took my MIL

> an

> > > hour or two to

> > > find him. When she did, he was wandering

> aimlessly

> > > around in the

> > > church parking lot. Now, he can no longer

> bathe

> > > himself or shampoo

> > > his hair. He has to have help going to the

> > > bathroom, getting

> > > dressed, getting into and out of cars, chairs,

> and

> > > bed. He's having

> > > some swallowing difficulties and urinary

> > > incontinence. He has to

> > > have help walking. He is delusional and

> obsessive

> > > (particularly

> > > about guns). The Sinemet he's on doesn't seem

> to

> > > help, at all,

> > > other than controlling his tremors somewhat.

> He has

> > > terrible

> > > freezing episodes and gets so rigid he can

> barely

>

=== message truncated ===

__________________________________________________

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  • 2 weeks later...
Guest guest

Bob,

May your mother rest in Peace. Sounds like many people clebrated your Mom's

life with you and your support system is a wonderful thing to have in place.

Come back and visit with us once in a while and let us know how you are doing.

Donna R

Do you want to read more about Lewy Body? You can also read the Thistle, the

LBD Newsletter. Just click on:

http://www.lewybodydementia.org

Thank you

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