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Hi Misty,

When I was implanted 12 years ago, the criteria was that you had NO

amplifiable hearing in either ear. Based on that, I was profoundly deaf

in both ears. Dr. implanted the one that had been deaf the longest (20

years), because if it didn't work, I would be no worse off than before.

It took about 3 months for sounds to be the way I remembered them

being. I'd worn hearing aids for a long time before being implanted, but

never had any stimulation in the ear that was implanted.

I talk on the phone, understand conversations without lipreading, and

function much as a hearing person.

Results vary, but mine turned out to be fantastic. I still do not

have an implant in the other ear, so all my hearing comes through the

implant, since the other ear is still too deaf to even use a hearing aid.

Is there anyone out there who was profoundly deaf and then implanted

who can tell me how it worked for them? Where you able to hear speech

and understand it? How long did it take to have benefits? Thanks,

Misty

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Hi ,

I'm not sure that " having no amplifiable hearing " is the right term here.

Cause many CI users still had some " amplifiable hearing " in their

implanted ear prior to the implantation. And that many also wore an

hearing aid in the implanted ear before the CI.

However, perhaps you meant that the criteria was that the user had

either very poor or hardly any or even zero speech recognition in the

implanted ear ? That is hardly or having difficulty understanding

speech without any visual clues ?

Dan

-- In , M Jansen <nucleus24@...> wrote:

>

> Hi Misty,

> When I was implanted 12 years ago, the criteria was that you had NO

> amplifiable hearing in either ear. Based on that, I was profoundly deaf

> in both ears. Dr. implanted the one that had been deaf the longest (20

> years), because if it didn't work, I would be no worse off than before.

> It took about 3 months for sounds to be the way I remembered them

> being. I'd worn hearing aids for a long time before being

implanted, but

> never had any stimulation in the ear that was implanted.

> I talk on the phone, understand conversations without lipreading, and

> function much as a hearing person.

> Results vary, but mine turned out to be fantastic. I still do not

> have an implant in the other ear, so all my hearing comes through the

> implant, since the other ear is still too deaf to even use a hearing

aid.

>

>

>

> Is there anyone out there who was profoundly deaf and then implanted

> who can tell me how it worked for them? Where you able to hear speech

> and understand it? How long did it take to have benefits? Thanks,

> Misty

> ____________________________________________________________

> Make the right POS decision. Click here for POS systems that meet

your business needs.

>

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>

>

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Dan,

In the early days of CI, you could have no amplifiable hearing to get CI.

The criteria has changed to 60% or worse in the better ear & 50% or worse in

the worse ear.

Re:profoundly deaf

Hi ,

I'm not sure that " having no amplifiable hearing " is the right term here.

Cause many CI users still had some " amplifiable hearing " in their

implanted ear prior to the implantation. And that many also wore an

hearing aid in the implanted ear before the CI.

However, perhaps you meant that the criteria was that the user had

either very poor or hardly any or even zero speech recognition in the

implanted ear ? That is hardly or having difficulty understanding

speech without any visual clues ?

Dan

-- In , M Jansen <nucleus24@...> wrote:

>

> Hi Misty,

> When I was implanted 12 years ago, the criteria was that you had NO

> amplifiable hearing in either ear. Based on that, I was profoundly deaf

> in both ears. Dr. implanted the one that had been deaf the longest (20

> years), because if it didn't work, I would be no worse off than before.

> It took about 3 months for sounds to be the way I remembered them

> being. I'd worn hearing aids for a long time before being

implanted, but

> never had any stimulation in the ear that was implanted.

> I talk on the phone, understand conversations without lipreading, and

> function much as a hearing person.

> Results vary, but mine turned out to be fantastic. I still do not

> have an implant in the other ear, so all my hearing comes through the

> implant, since the other ear is still too deaf to even use a hearing

aid.

>

>

>

> Is there anyone out there who was profoundly deaf and then implanted

> who can tell me how it worked for them? Where you able to hear speech

> and understand it? How long did it take to have benefits? Thanks,

> Misty

> ____________________________________________________________

> Make the right POS decision. Click here for POS systems that meet

your business needs.

>

http://thirdpartyoffers.juno.com/TGL2141/fc/Ioyw6i3l5GmhUPqbMv9sJGEoWFbyux1xOfj0\

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>

>

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Dan,

What is talking about is back in the old days, one had to have no

" useful " hearing to qualify.

One can have " enough " hearing to amplify it with a HA and still not gain

any speech understanding.

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Re:profoundly deaf

> Hi ,

>

> I'm not sure that " having no amplifiable hearing " is the right term here.

>

> Cause many CI users still had some " amplifiable hearing " in their

> implanted ear prior to the implantation. And that many also wore an

> hearing aid in the implanted ear before the CI.

>

> However, perhaps you meant that the criteria was that the user had

> either very poor or hardly any or even zero speech recognition in the

> implanted ear ? That is hardly or having difficulty understanding

> speech without any visual clues ?

>

> Dan

>

> -- In , M Jansen <nucleus24@...> wrote:

>>

>> Hi Misty,

>> When I was implanted 12 years ago, the criteria was that you had NO

>> amplifiable hearing in either ear. Based on that, I was profoundly deaf

>> in both ears. Dr. implanted the one that had been deaf the longest (20

>> years), because if it didn't work, I would be no worse off than before.

>> It took about 3 months for sounds to be the way I remembered them

>> being. I'd worn hearing aids for a long time before being

> implanted, but

>> never had any stimulation in the ear that was implanted.

>> I talk on the phone, understand conversations without lipreading, and

>> function much as a hearing person.

>> Results vary, but mine turned out to be fantastic. I still do not

>> have an implant in the other ear, so all my hearing comes through the

>> implant, since the other ear is still too deaf to even use a hearing

> aid.

>>

>>

>>

>> Is there anyone out there who was profoundly deaf and then implanted

>> who can tell me how it worked for them? Where you able to hear speech

>> and understand it? How long did it take to have benefits? Thanks,

>> Misty

>> ____________________________________________________________

>> Make the right POS decision. Click here for POS systems that meet

> your business needs.

>>

>

http://thirdpartyoffers.juno.com/TGL2141/fc/Ioyw6i3l5GmhUPqbMv9sJGEoWFbyux1xOfj0\

HKCGhjtD2hZpeFZm7p/

>>

>>

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Dan

is speaking about HER OWN experience, 12 YEARS ago. She and

some others here, were among the first to be implanted and as thus,

were our pioneers.

I think it would have taken infinitely more courage to get an implant

back then. They didnt have the benefit of a group such as this, where

people are kind enough to share THEIR OWN experiences, with others, to

hopefully make the new persons journey less stressful and less scary

and to give them hope for a better present and future.

is an eloquent lady who expresses herself well, I'm quite sure

she wrote about what SHE KNOWS.

Just think, in 12 years, you will also have the benefit of 12 years

experience and all the benefits of hindsight that go with it :-).

Ted F.

> >

> > Hi Misty,

> > When I was implanted 12 years ago, the criteria was that you had NO

> > amplifiable hearing in either ear. Based on that, I was

profoundly deaf

> > in both ears. Dr. implanted the one that had been deaf the

longest (20

> > years), because if it didn't work, I would be no worse off than

before.

> > It took about 3 months for sounds to be the way I remembered them

> > being. I'd worn hearing aids for a long time before being

> implanted, but

> > never had any stimulation in the ear that was implanted.

> > I talk on the phone, understand conversations without

lipreading, and

> > function much as a hearing person.

> > Results vary, but mine turned out to be fantastic. I still do not

> > have an implant in the other ear, so all my hearing comes through the

> > implant, since the other ear is still too deaf to even use a hearing

> aid.

> >

> >

> >

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Dan, my good man,

I said what I meant, and I meant what I said. 12 years ago when I was

implanted a candidate could have NO amplifiable hearing in either ear.

Which means a hearing aid wouldn't work AT ALL in EITHER EAR. Speech

recognition was not even considered. If you could hear an airplane you

had amplifiable hearing. I could hear nothing, nada, etc.

The criteria has changed since then, in that one can now have up to

60% speech comprehension in the better ear, and 40% in the worse ear (may

have changed from that as well). But 12 years ago during clinical trials

for the Nucleus 24 straight array - which I have - you could not use a

hearing aid in either ear and get an implant. You had to be deaf as a

post. And I was.

Hi ,

I'm not sure that " having no amplifiable hearing " is the right term here.

Cause many CI users still had some " amplifiable hearing " in their

implanted ear prior to the implantation. And that many also wore an

hearing aid in the implanted ear before the CI.

However, perhaps you meant that the criteria was that the user had

either very poor or hardly any or even zero speech recognition in the

implanted ear ? That is hardly or having difficulty understanding

speech without any visual clues ?

Dan

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Hi Ted & & all,

Thanks for jumping in and repeating what I said in the first place.

12 years ago you had to have NO amplifiable hearing in order to get a

cochlear implant.

I like to think I express myself adequately, and that there is not too

much room for misunderstanding, but who knows. There are other blondes

out there besides myself.

Thanks to all for clarifying what the criteria was WAY BACK when - 12

years ago - when I was a pioneer woman.

Dan

is speaking about HER OWN experience, 12 YEARS ago. She and

some others here, were among the first to be implanted and as thus,

were our pioneers.

I think it would have taken infinitely more courage to get an implant

back then. They didnt have the benefit of a group such as this, where

people are kind enough to share THEIR OWN experiences, with others, to

hopefully make the new persons journey less stressful and less scary

and to give them hope for a better present and future.

is an eloquent lady who expresses herself well, I'm quite sure

she wrote about what SHE KNOWS.

Just think, in 12 years, you will also have the benefit of 12 years

experience and all the benefits of hindsight that go with it :-).

Ted F.

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Not a problem . We all, well most all, understood you just fine

because we know that the criteria has changed in recent years. You said

what you meant and meant what you said. Right on. If there is still a

doubting here, well, oh well.

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Newport, Oregon

N24C 8/2000 Hookup

rclark0276@...

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I haven't posted in ages and just popped in to see what was going on

and came across this subject and thought I just mention my

circumstances.

I lost my hearing suddently and was implanted just " 4 " years ago

Oct. 2004, and was told one of the criterias was I had to be

profoundly deaf, I even had to wear one of their hearing aids before

the surgery just to prove that it did not help me, " which it didn't "

I have come to realize when it comes to CI's things are changing all

the time. I just read a post on my LDA (Late deafened adult) group

where a member was implanted and was able to wash her hair the next

day. (as long as she kept her incision dry) 4 years ago I was told

to wait weeks. THis may also have something to do with the Dr.

Just giving my 2cents.

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Alright . Cause I do know a couple of CI users that were

actually very good hearing aid wearers. They had good amplifiable

hearing, good speech and all that. And had gotten their implant about

10 years ago. Perhaps, the criteria was starting to change a bit

then. No problem.

Dan

>

> Dan, my good man,

> I said what I meant, and I meant what I said. 12 years ago when

I was

> implanted a candidate could have NO amplifiable hearing in either

ear.

> Which means a hearing aid wouldn't work AT ALL in EITHER EAR.

Speech

> recognition was not even considered. If you could hear an airplane

you

> had amplifiable hearing. I could hear nothing, nada, etc.

>

> The criteria has changed since then, in that one can now have

up to

> 60% speech comprehension in the better ear, and 40% in the worse

ear (may

> have changed from that as well). But 12 years ago during clinical

trials

> for the Nucleus 24 straight array - which I have - you could not

use a

> hearing aid in either ear and get an implant. You had to be deaf

as a

> post. And I was.

>

>

>

> Hi ,

>

> I'm not sure that " having no amplifiable hearing " is the right term

here.

>

> Cause many CI users still had some " amplifiable hearing " in their

> implanted ear prior to the implantation. And that many also wore an

> hearing aid in the implanted ear before the CI.

>

> However, perhaps you meant that the criteria was that the user had

> either very poor or hardly any or even zero speech recognition in

the

> implanted ear ? That is hardly or having difficulty understanding

> speech without any visual clues ?

>

> Dan

> ____________________________________________________________

> Save on Trade Schools - Click here.

>

http://thirdpartyoffers.juno.com/TGL2141/fc/Ioyw6i3oLawOmNF6UphU3aDPmf

5zWgJj2KjGcL2883ZKIDYvikHsR9/

>

>

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,

Another concern I had was that I felt that it wasn't the first time

I've come across such posts, articles or sources that made it look

like a cochlear implant would enable one to go from " hearing nothing

at all " to " bingo ! that person has been cured and now

hearings 'normally' " . Cause that's usually not the case. It's usually

somewhat in between.

But like you and the others pointed out, perhaps the criteria was

different back then. No problem.

Dan

>

> Dan, my good man,

> I said what I meant, and I meant what I said. 12 years ago when

I was

> implanted a candidate could have NO amplifiable hearing in either

ear.

> Which means a hearing aid wouldn't work AT ALL in EITHER EAR.

Speech

> recognition was not even considered. If you could hear an airplane

you

> had amplifiable hearing. I could hear nothing, nada, etc.

>

> The criteria has changed since then, in that one can now have

up to

> 60% speech comprehension in the better ear, and 40% in the worse

ear (may

> have changed from that as well). But 12 years ago during clinical

trials

> for the Nucleus 24 straight array - which I have - you could not

use a

> hearing aid in either ear and get an implant. You had to be deaf

as a

> post. And I was.

>

>

>

> Hi ,

>

> I'm not sure that " having no amplifiable hearing " is the right term

here.

>

> Cause many CI users still had some " amplifiable hearing " in their

> implanted ear prior to the implantation. And that many also wore an

> hearing aid in the implanted ear before the CI.

>

> However, perhaps you meant that the criteria was that the user had

> either very poor or hardly any or even zero speech recognition in

the

> implanted ear ? That is hardly or having difficulty understanding

> speech without any visual clues ?

>

> Dan

> ____________________________________________________________

> Save on Trade Schools - Click here.

>

http://thirdpartyoffers.juno.com/TGL2141/fc/Ioyw6i3oLawOmNF6UphU3aDPmf

5zWgJj2KjGcL2883ZKIDYvikHsR9/

>

>

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Dan,

Anyone who tells you a CI makes you hear like normal has a few screws

missing. It certainly is way lots better than not hearing anything at

all, but it does not compare to typical hearing that a person with no

hearing loss has. But it's the best that is available for those who

otherwise have no hearing at all.

When they first started doing implants, they would do them on folks

with no hearing because then you were no worse off if it didn't work.

Then they started doing for folks who has some residual hearing in the

ear that wouldn't be implanted. Then they started doing for folks who

had some hearing in the ear that would be implanted, just not enough

residual hearing to be of much value. Being able to hear an airplane

flying overhed, or a fire engine, but nothing quieter than that isn't

much use in understanding speech.

They also used to implant people who had typical hearing most of their

lives, and wouldn't dream of implanting someone who never heard, because

they had no auditory memory. No matter how great their lipreading skills

were, they had no memory of sound. That, too, has changed, and many pre

lingually deafened adults are now getting implants. Their results differ

drastically from people who had hearing at one time, lost it, but still

have auditory memory of what sounds are like.

,

Another concern I had was that I felt that it wasn't the first time

I've come across such posts, articles or sources that made it look

like a cochlear implant would enable one to go from " hearing nothing

at all " to " bingo ! that person has been cured and now

hearings 'normally' " . Cause that's usually not the case. It's usually

somewhat in between.

But like you and the others pointed out, perhaps the criteria was

different back then. No problem.

Dan

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- I think you may have the criteria a little mixed up, though

close. The key term was " benefit " . One had to be at the point where

hearing aids were of NO benefit. This was important because if one

had some benefit, they needed to be sure that the probability of

coming out of surgery with less speech comprehension than going into

surgery was low.

Twelve years ago I was profoundly deaf and decided against getting a

CI. The changes in the standards of qualification for CI can be

understood in terms of the humungous variance in speech comprehension

scores back then. There was a high probability that a person who

could comprehend 30% of monosyllabic words would post surgically

comprehend less than before surgery. The mean scores stayed at

between 38% and 43% for a long time. It is far more recent that the

mean score increased while the standard deviation decreased. It is

now improbable (not impossible) that a person will comprehend less

after surgery than before. Twelve years ago they could not say

that. Of course they still notify candidates that results are not

predictable.

The variance ini results was a major factor in my choosing to learn

sign language in my waiting to get a CI. And by the way all the

folks who tried to tell me 12 years ago that I wouldn't be able to

benefit from a CI in the future because my auditory nerve being under-

stimulated -- well those idiots were WRONG. With my first CI I get

100% in lab conditions. My second CI is still being remapped (again

this thursday). I am not near as impressed with the second as with

the first -- but I am sure the auditory nerve is just fine. With the

first CI it is easy, including when listening to music, to forget I

have CI. With the second CI, it reminds me in a very annoying way.

Tinnitus still rages and I still find myself questioning why I was so

stupid as to think 100% could be improved upon by getting a second CI.

>

> Dan, my good man,

> I said what I meant, and I meant what I said. 12 years ago when

I was

> implanted a candidate could have NO amplifiable hearing in either

ear.

> Which means a hearing aid wouldn't work AT ALL in EITHER EAR.

Speech

> recognition was not even considered. If you could hear an airplane

you

> had amplifiable hearing. I could hear nothing, nada, etc.

>

> The criteria has changed since then, in that one can now have

up to

> 60% speech comprehension in the better ear, and 40% in the worse

ear (may

> have changed from that as well). But 12 years ago during clinical

trials

> for the Nucleus 24 straight array - which I have - you could not

use a

> hearing aid in either ear and get an implant. You had to be deaf

as a

> post. And I was.

>

>

>

> Hi ,

>

> I'm not sure that " having no amplifiable hearing " is the right term

here.

>

> Cause many CI users still had some " amplifiable hearing " in their

> implanted ear prior to the implantation. And that many also wore an

> hearing aid in the implanted ear before the CI.

>

> However, perhaps you meant that the criteria was that the user had

> either very poor or hardly any or even zero speech recognition in

the

> implanted ear ? That is hardly or having difficulty understanding

> speech without any visual clues ?

>

> Dan

> ____________________________________________________________

> Save on Trade Schools - Click here.

>

http://thirdpartyoffers.juno.com/TGL2141/fc/Ioyw6i3oLawOmNF6UphU3aDPmf

5zWgJj2KjGcL2883ZKIDYvikHsR9/

>

>

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