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Re: speech/bulbar help

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>Hello to all with speech problems,

>

>You do not have to be isolated from friends, family and business

>communication because you cannot speak! No aid is as easy as the days

>we could talk and sing, but with patience you can function without

>the exhaustion of trying to be understood by others. There are two

>things I use to communicate, and anyone has access to these aids.

>

>1. I have a voiced computer. Go to www.synapsePLS.org then click

>Internet Resources and scroll down to speech devices. I have an

>Enkidu device. Enkidu has now been purchased by Dynavox, but you can

>reach Enkidu through the site listed. Some folks have a LightWriter.

>A voiced computer is durable medical goods, which is covered by

>insurance. Your neurologist, primary care, or an assistive device

>specialist at a rehab will write a detailed letter to your insurance

>company explaining your need. (I live outside Boston, and my request

>was handled by Spaulding Rehab Hospital.) I was advised to apply

>before my need was desperate, as it takes awhle to get one. I've had

>it for a year now, and I'd be lost without it.

But don't get your hopes up too high. I have tried several many speech

synthesis devices, and with most of them you have to spell out the word

before it is dealt with. Even with various types of " word prediction "

(where the software tries to guess what you are going to say -- faster

processors and memory can increase capabilities, but I've found nothing

that would let me participate in a conversation like I used to) it is still

painfully slow for me,

>2. I learned sign language, and so has Jim, my husband, as well as my

>adult kids and their kids. Go to

>http://where.com/scott.net/asl/abc.html and print out the alphabet,

>hand out copies to your loved ones. Often times Jim can understand

>over half of what I say and if I hand spell a word or two he gets it.

>It's actually fun for kids, as they can " talk " to each other across a

>room! Anyone coming to TeamWalk and the Conference, get busy and

>learn it, and we can " talk " .

In my experience it only works if who you are " talking " to invests some

time in learning themselves. Much of the American Sign Language means

little to people who know nothing about it. Finger spelling is essentially

worthless unless the person you are trying to communicate with not only

knows something about it, but is aware of what you are doing to boot.

>I'll tell you more about how I manage if you are interested. The key

>is not to shut down. Technology exists for us to still be able to

>interact with others. You will find that alot is demanded of the

>listener, and some aren't patient, but. . . that is their handicap,

>not yours!

>

>Thurza

I realize that, but aside from fixing blame there is trying to function in

a world where most expect you to communicate in a way you no longer can.

Don't get me wrong, the above can be great, but for general communication

with chance encounters (sales clerks, parking attendants, delivery people,

etc.) I find simple gestures to be the most effective. I use techniques

like the above when I have someone along who can help " translate, " but when

I'm on my own (which is most times), even though it may be *their* fault,

I'm the one who has to deal with it.

Sorry to be such a wet blanket, but that's just the way things work in my

little corner of the world.

__

Galen Hekhuis NpD, JFR, GWA ghekhuis@...

Illiterate? Write for FREE help

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Since my Mother passed away in January all of her lifelong quotes keep

coming back....not that she was the only to ever say it but.... " The Lord helps

those who help themselves "

was one of her biggies....sounds like it fits perfectly here in using a

speech augmentation device. In Fremont where we live we have the School for

the

Blind and School for the Deaf which (I think) is the only one in northern

California so it's a very large campus. I'm used to seeing people of all ages

signing but of course it's big here and the junior college has sign languages

classes. I have said before how much I miss singing and I truly do because

it was a big part of my life. Last Sunday in church I was " down " because I

wanted so badly to join in and then I glanced over to my right and here was

this woman signing and " singing " to her heart's content. Can't say that my

eyes

stayed dry.

Alone we can do so little. Together we can do so much.

Helen Keller (1880-1968)

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Thurza,

As I wrote to you in February, I lost my voice completely after my stroke.

It didn't come back to the poor speech it was in prior to the stroke. I

have been working with a speech therapist since February to get a speech

augmentation device and yesterday I was informed that my secondary insurance

had approved it after they had initially rejected the claim. I should

getting a Enkidu Tablet XL Impact D and a wheelchair mount for it in 2 to 3

weeks. WHOPPEE!!!

speech/bulbar help

>

> Hello to all with speech problems,

>

> You do not have to be isolated from friends, family and business

> communication because you cannot speak! No aid is as easy as the days

> we could talk and sing, but with patience you can function without

> the exhaustion of trying to be understood by others. There are two

> things I use to communicate, and anyone has access to these aids.

>

> 1. I have a voiced computer. Go to www.synapsePLS.org then click

> Internet Resources and scroll down to speech devices. I have an

> Enkidu device. Enkidu has now been purchased by Dynavox, but you can

> reach Enkidu through the site listed. Some folks have a LightWriter.

> A voiced computer is durable medical goods, which is covered by

> insurance. Your neurologist, primary care, or an assistive device

> specialist at a rehab will write a detailed letter to your insurance

> company explaining your need. (I live outside Boston, and my request

> was handled by Spaulding Rehab Hospital.) I was advised to apply

> before my need was desperate, as it takes awhle to get one. I've had

> it for a year now, and I'd be lost without it.

>

> 2. I learned sign language, and so has Jim, my husband, as well as my

> adult kids and their kids. Go to

> http://where.com/scott.net/asl/abc.html and print out the alphabet,

> hand out copies to your loved ones. Often times Jim can understand

> over half of what I say and if I hand spell a word or two he gets it.

> It's actually fun for kids, as they can " talk " to each other across a

> room! Anyone coming to TeamWalk and the Conference, get busy and

> learn it, and we can " talk " .

>

> I'll tell you more about how I manage if you are interested. The key

> is not to shut down. Technology exists for us to still be able to

> interact with others. You will find that alot is demanded of the

> listener, and some aren't patient, but. . . that is their handicap,

> not yours!

>

> Thurza

>

>

>

>

>

>

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: I once went to a dinner theater and several deaf people were

at a nearby table. An interpreter signed the whole play, and it was

the most extraordinary thing I'd ever seen. I just watched her, not

the play, because she was so expressive. So go on and sing with your

hands...it's wonderful.

Edith

> Since my Mother passed away in January all of her lifelong quotes

keep

> coming back....not that she was the only to ever say it

but.... " The Lord helps

> those who help themselves "

> was one of her biggies....sounds like it fits perfectly here in

using a

> speech augmentation device. In Fremont where we live we have the

School for the

> Blind and School for the Deaf which (I think) is the only one in

northern

> California so it's a very large campus. I'm used to seeing

people of all ages

> signing but of course it's big here and the junior college has

sign languages

> classes. I have said before how much I miss singing and I truly

do because

> it was a big part of my life. Last Sunday in church I was " down "

because I

> wanted so badly to join in and then I glanced over to my right

and here was

> this woman signing and " singing " to her heart's content. Can't

say that my eyes

> stayed dry.

>

>

>

> Alone we can do so little. Together we can do so much.

> Helen Keller (1880-1968)

>

>

>

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