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Re: Approved for CCRS

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In a message dated 1/6/2004 2:47:19 PM Eastern Standard Time,

design@... writes:

> >Can anyone tell me if this is true?

> >I was under the impression that they had aids that only amplify the high

> >frequencies, and you don't have to have a low frequency loss to wear them.

> >I think she is thinking standard aids and not specifically high frequency

> >ones. I don't know, and most on here aren't dealing with a low dB loss

> like

> >we are. She also said they start aiding usually at 30 dB, but not in this

> >case, but I questioned her on this about how kids show adverse effects

> >educationally with a 16 dB loss, and she was like yes but they don't aid

> >them. Well maybe they don't but many people do, and I am a little anoyd

> >that they don't.

>

When our son was initially diagnosed, his loses were 25-30 db in his right

ear and 15-20 in his left. The audiologist told us that the 15 db loss should be

aided as well. He was rather adamant about it, but our son was not at all

thrilled with the idea of 2 aides. However, Ian did want one. So we compromised

and at first we aided his " bad " ear, the right. He got so much help from that

one aide that he asked for the second one even before our aggreed " testing

time " was up. Unlike other kids we'd heard about, Ian LOVED his aides and has

never fought them.

We were also fighting with the school district, trying to force them to

recognize Ian's hearing loss as being educationally significant and to classify

him. The audiologist pointed us to several studies which showed that a 15 db

loss

can have significant adverse affects on education. He also mapped Ian's

audiograms onto a chart that contained a pale blue banana shape and little

labels

as to where spoken sounds are heard in standard conversation. We took that with

us to the next IEP as documentation proving just how our son's loss was

impacting his ability to access the information/education in the classroom. I

don't

remember where the studies were done, and I cannot lay my hands on that file

right now. It was about 5 years ago, so I don't know where I've filed it.

So, you are correct in thinking that a 15 db loss is important. Ian's loss

now drops down to 50-55 db loss in both ears for all the mid-range frequencies.

In retrospect, I wish we'd aided that other ear sooner -- the sooner he would

have had access to more language. But we followed his lead and did it the

right way for him.

Best of luck - Jill

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In a message dated 1/6/2004 2:47:19 PM Eastern Standard Time,

design@... writes:

> >Can anyone tell me if this is true?

> >I was under the impression that they had aids that only amplify the high

> >frequencies, and you don't have to have a low frequency loss to wear them.

> >I think she is thinking standard aids and not specifically high frequency

> >ones. I don't know, and most on here aren't dealing with a low dB loss

> like

> >we are. She also said they start aiding usually at 30 dB, but not in this

> >case, but I questioned her on this about how kids show adverse effects

> >educationally with a 16 dB loss, and she was like yes but they don't aid

> >them. Well maybe they don't but many people do, and I am a little anoyd

> >that they don't.

>

When our son was initially diagnosed, his loses were 25-30 db in his right

ear and 15-20 in his left. The audiologist told us that the 15 db loss should be

aided as well. He was rather adamant about it, but our son was not at all

thrilled with the idea of 2 aides. However, Ian did want one. So we compromised

and at first we aided his " bad " ear, the right. He got so much help from that

one aide that he asked for the second one even before our aggreed " testing

time " was up. Unlike other kids we'd heard about, Ian LOVED his aides and has

never fought them.

We were also fighting with the school district, trying to force them to

recognize Ian's hearing loss as being educationally significant and to classify

him. The audiologist pointed us to several studies which showed that a 15 db

loss

can have significant adverse affects on education. He also mapped Ian's

audiograms onto a chart that contained a pale blue banana shape and little

labels

as to where spoken sounds are heard in standard conversation. We took that with

us to the next IEP as documentation proving just how our son's loss was

impacting his ability to access the information/education in the classroom. I

don't

remember where the studies were done, and I cannot lay my hands on that file

right now. It was about 5 years ago, so I don't know where I've filed it.

So, you are correct in thinking that a 15 db loss is important. Ian's loss

now drops down to 50-55 db loss in both ears for all the mid-range frequencies.

In retrospect, I wish we'd aided that other ear sooner -- the sooner he would

have had access to more language. But we followed his lead and did it the

right way for him.

Best of luck - Jill

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In a message dated 1/6/2004 2:47:19 PM Eastern Standard Time,

design@... writes:

> >Can anyone tell me if this is true?

> >I was under the impression that they had aids that only amplify the high

> >frequencies, and you don't have to have a low frequency loss to wear them.

> >I think she is thinking standard aids and not specifically high frequency

> >ones. I don't know, and most on here aren't dealing with a low dB loss

> like

> >we are. She also said they start aiding usually at 30 dB, but not in this

> >case, but I questioned her on this about how kids show adverse effects

> >educationally with a 16 dB loss, and she was like yes but they don't aid

> >them. Well maybe they don't but many people do, and I am a little anoyd

> >that they don't.

>

When our son was initially diagnosed, his loses were 25-30 db in his right

ear and 15-20 in his left. The audiologist told us that the 15 db loss should be

aided as well. He was rather adamant about it, but our son was not at all

thrilled with the idea of 2 aides. However, Ian did want one. So we compromised

and at first we aided his " bad " ear, the right. He got so much help from that

one aide that he asked for the second one even before our aggreed " testing

time " was up. Unlike other kids we'd heard about, Ian LOVED his aides and has

never fought them.

We were also fighting with the school district, trying to force them to

recognize Ian's hearing loss as being educationally significant and to classify

him. The audiologist pointed us to several studies which showed that a 15 db

loss

can have significant adverse affects on education. He also mapped Ian's

audiograms onto a chart that contained a pale blue banana shape and little

labels

as to where spoken sounds are heard in standard conversation. We took that with

us to the next IEP as documentation proving just how our son's loss was

impacting his ability to access the information/education in the classroom. I

don't

remember where the studies were done, and I cannot lay my hands on that file

right now. It was about 5 years ago, so I don't know where I've filed it.

So, you are correct in thinking that a 15 db loss is important. Ian's loss

now drops down to 50-55 db loss in both ears for all the mid-range frequencies.

In retrospect, I wish we'd aided that other ear sooner -- the sooner he would

have had access to more language. But we followed his lead and did it the

right way for him.

Best of luck - Jill

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In a message dated 1/6/2004 2:34:38 PM Eastern Standard Time,

enriquez16@... writes:

I would really like to know what LE means

Perhaps it means " left ear " I'm guessing. I don't know the specifics on the

hearing aid question but I assumed the programmables were suited to adjust

for low and high frequency. My son has the Phonic Ear Sono Forte programmables

and the audi adjusts those specifically to his hearing loss in the different

frequencies.

's mom, 3yrs, CI 7/30/02

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In a message dated 1/6/2004 2:34:38 PM Eastern Standard Time,

enriquez16@... writes:

I would really like to know what LE means

Perhaps it means " left ear " I'm guessing. I don't know the specifics on the

hearing aid question but I assumed the programmables were suited to adjust

for low and high frequency. My son has the Phonic Ear Sono Forte programmables

and the audi adjusts those specifically to his hearing loss in the different

frequencies.

's mom, 3yrs, CI 7/30/02

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In a message dated 1/6/2004 2:34:38 PM Eastern Standard Time,

enriquez16@... writes:

I would really like to know what LE means

Perhaps it means " left ear " I'm guessing. I don't know the specifics on the

hearing aid question but I assumed the programmables were suited to adjust

for low and high frequency. My son has the Phonic Ear Sono Forte programmables

and the audi adjusts those specifically to his hearing loss in the different

frequencies.

's mom, 3yrs, CI 7/30/02

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HI ,

My daughter's hearing loss is worse in the low freq. She has a

moderate rising to mild loss. We were discussing hearing aids today and are

going

with digital. I asked about being able to program each freq. and increasing the

low freq. Her audi told me that they do not like to amplify the low freq to

much because they can easily be overamplified and actually make speech

recognition worse if they are overamplified. I don't know if this is what you

audi

meant or not but I thought I would mention it.

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HI ,

My daughter's hearing loss is worse in the low freq. She has a

moderate rising to mild loss. We were discussing hearing aids today and are

going

with digital. I asked about being able to program each freq. and increasing the

low freq. Her audi told me that they do not like to amplify the low freq to

much because they can easily be overamplified and actually make speech

recognition worse if they are overamplified. I don't know if this is what you

audi

meant or not but I thought I would mention it.

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-

PDHH has audiologists on that list that can answer these audiology

questions. Not only are they audiologists - they also have children who are

deaf. I know that one of the audiologists has children with other needs

besides being deaf.

Have your doctors looked into having auditory neuropathy?

Or CAPD?

>

_________________________________________________________________

Get reliable dial-up Internet access now with our limited-time introductory

offer. http://join.msn.com/?page=dept/dialup

Link to comment
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-

PDHH has audiologists on that list that can answer these audiology

questions. Not only are they audiologists - they also have children who are

deaf. I know that one of the audiologists has children with other needs

besides being deaf.

Have your doctors looked into having auditory neuropathy?

Or CAPD?

>

_________________________________________________________________

Get reliable dial-up Internet access now with our limited-time introductory

offer. http://join.msn.com/?page=dept/dialup

Link to comment
Share on other sites

-

PDHH has audiologists on that list that can answer these audiology

questions. Not only are they audiologists - they also have children who are

deaf. I know that one of the audiologists has children with other needs

besides being deaf.

Have your doctors looked into having auditory neuropathy?

Or CAPD?

>

_________________________________________________________________

Get reliable dial-up Internet access now with our limited-time introductory

offer. http://join.msn.com/?page=dept/dialup

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Just wanted to let you know , that my son Ian wears digital aids for

high frequency loss ONLY.. they can program the digital aids to amplify only

what your son needs. ALSO, on the school issue... get the book " NO CHILD

LEFT BEHIND " , that comes from a Mom of a child with Angelman's Syndrome who

had to fight for her son's rights to get a public funded education.

--

Thanks,

Tillery

Birmingham, AL

Ian (3-1/2 yrs HI Moderate/Severe - Aids)

Emma (7 yrs Hearing)

on 1/6/04 1:11 PM, Joe & at enriquez16@... wrote:

> Can anyone tell me if this is true?

> I was under the impression that they had aids that only amplify the high

> frequencies, and you don't have to have a low frequency loss to wear them.

> I think she is thinking standard aids and not specifically high frequency

> ones. I don't know, and most on here aren't dealing with a low dB loss like

> we are. She also said they start aiding usually at 30 dB, but not in this

> case, but I questioned her on this about how kids show adverse effects

> educationally with a 16 dB loss, and she was like yes but they don't aid

> them. Well maybe they don't but many people do, and I am a little anoyd

> that they don't.

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Share on other sites

Just wanted to let you know , that my son Ian wears digital aids for

high frequency loss ONLY.. they can program the digital aids to amplify only

what your son needs. ALSO, on the school issue... get the book " NO CHILD

LEFT BEHIND " , that comes from a Mom of a child with Angelman's Syndrome who

had to fight for her son's rights to get a public funded education.

--

Thanks,

Tillery

Birmingham, AL

Ian (3-1/2 yrs HI Moderate/Severe - Aids)

Emma (7 yrs Hearing)

on 1/6/04 1:11 PM, Joe & at enriquez16@... wrote:

> Can anyone tell me if this is true?

> I was under the impression that they had aids that only amplify the high

> frequencies, and you don't have to have a low frequency loss to wear them.

> I think she is thinking standard aids and not specifically high frequency

> ones. I don't know, and most on here aren't dealing with a low dB loss like

> we are. She also said they start aiding usually at 30 dB, but not in this

> case, but I questioned her on this about how kids show adverse effects

> educationally with a 16 dB loss, and she was like yes but they don't aid

> them. Well maybe they don't but many people do, and I am a little anoyd

> that they don't.

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Share on other sites

Just wanted to let you know , that my son Ian wears digital aids for

high frequency loss ONLY.. they can program the digital aids to amplify only

what your son needs. ALSO, on the school issue... get the book " NO CHILD

LEFT BEHIND " , that comes from a Mom of a child with Angelman's Syndrome who

had to fight for her son's rights to get a public funded education.

--

Thanks,

Tillery

Birmingham, AL

Ian (3-1/2 yrs HI Moderate/Severe - Aids)

Emma (7 yrs Hearing)

on 1/6/04 1:11 PM, Joe & at enriquez16@... wrote:

> Can anyone tell me if this is true?

> I was under the impression that they had aids that only amplify the high

> frequencies, and you don't have to have a low frequency loss to wear them.

> I think she is thinking standard aids and not specifically high frequency

> ones. I don't know, and most on here aren't dealing with a low dB loss like

> we are. She also said they start aiding usually at 30 dB, but not in this

> case, but I questioned her on this about how kids show adverse effects

> educationally with a 16 dB loss, and she was like yes but they don't aid

> them. Well maybe they don't but many people do, and I am a little anoyd

> that they don't.

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That's an idea... Ian was thought to have CAPD by his speech therapist in

the beginning & his AIDB (AL Institute for Deaf & Blind) Speech Therapist

told me that digital hearing aids would help this condition, as well as help

him if it was just a hearing loss we were facing. So either way digital aids

are the way to go.

--

Thanks,

Tillery

Birmingham, AL

Ian (3-1/2 yrs HI Moderate/Severe - Aids)

Emma (7 yrs Hearing)

on 1/6/04 1:19 PM, E. Mapa at maryemapa@... wrote:

> Have your doctors looked into having auditory neuropathy?

> Or CAPD?

>

>

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That's an idea... Ian was thought to have CAPD by his speech therapist in

the beginning & his AIDB (AL Institute for Deaf & Blind) Speech Therapist

told me that digital hearing aids would help this condition, as well as help

him if it was just a hearing loss we were facing. So either way digital aids

are the way to go.

--

Thanks,

Tillery

Birmingham, AL

Ian (3-1/2 yrs HI Moderate/Severe - Aids)

Emma (7 yrs Hearing)

on 1/6/04 1:19 PM, E. Mapa at maryemapa@... wrote:

> Have your doctors looked into having auditory neuropathy?

> Or CAPD?

>

>

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That's an idea... Ian was thought to have CAPD by his speech therapist in

the beginning & his AIDB (AL Institute for Deaf & Blind) Speech Therapist

told me that digital hearing aids would help this condition, as well as help

him if it was just a hearing loss we were facing. So either way digital aids

are the way to go.

--

Thanks,

Tillery

Birmingham, AL

Ian (3-1/2 yrs HI Moderate/Severe - Aids)

Emma (7 yrs Hearing)

on 1/6/04 1:19 PM, E. Mapa at maryemapa@... wrote:

> Have your doctors looked into having auditory neuropathy?

> Or CAPD?

>

>

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<<We were told aids couldn't help him because the frequencies were too high. His

loss is at 2000 and 4000 HZ.>>

I don't believe this is true. Up to at least 4000 HZ, the digital programmables

should be able to help. My son's loss on the right is 60 dB at 2000 HZ and 80 dB

at 4000. His AIDED responses at 2000 HZ are at 25 DB and at 4000 HZ his

response is at or above 40. Yes, they aren't totally corrected but I'm sure he'd

rather hear at 25 and 40 than not at all! has 3-year-old Oticon Digifocus

II's which have served us well but I understand that there are even more

powerful digitals out there for those who need them. I'd ask again...or ask

someone else!

Carol - mom to , 7.8, mod to profound, LVAS

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<<We were told aids couldn't help him because the frequencies were too high. His

loss is at 2000 and 4000 HZ.>>

I don't believe this is true. Up to at least 4000 HZ, the digital programmables

should be able to help. My son's loss on the right is 60 dB at 2000 HZ and 80 dB

at 4000. His AIDED responses at 2000 HZ are at 25 DB and at 4000 HZ his

response is at or above 40. Yes, they aren't totally corrected but I'm sure he'd

rather hear at 25 and 40 than not at all! has 3-year-old Oticon Digifocus

II's which have served us well but I understand that there are even more

powerful digitals out there for those who need them. I'd ask again...or ask

someone else!

Carol - mom to , 7.8, mod to profound, LVAS

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,

Thanks, I really should join that list, I am a little busy right now though

I have so many e-mails I don't know what is going on with that but when I

finish I will look up your previous e-mail and go to that site.

The doctors have considered AN but the difference between and AN is

that he has a response down to 25 dB in the low frequencies and 30 dB in the

high, which is not consistant with AN but very very similar to it. CAPD has

been ruled out because it is much more severe and there are physical things

that are causing his inability to understand the sound, but they aren't sure

that he doesn't have pure word deafness which technically is a form of CAPD

but not all CAPD is pure word deafness. I have a problem with giving him

the CAPD label because when doctors, educators, and parents think of it,

they think of a child who has difficulty hearing and understanding things,

being worse in noisy situations, but doesn't even respond to the sound,

so it's not just a matter of him not understanding it, we believe that all

sound, sounds the same so he doesn't respond to it. He does however know

the sound of the TV but won't even respond to his name. He will sometimes

say dada if we make that sound, if he is really focused sometimes I sign and

say mmmmmama and he will say baba, because it looks the same, he coppies E

and makes vowel sounds, but that's it. He is not hearing well at all. So I

am wanting services as HI child because speech therapists have said that

while we should keep working with him on responding to verbal sounds, it is

very unlikely he will ever be a speaker. I just don't want him in a class

where the focus is getting him to talk. I do want them to work on that

though, I don't want them to give up, but my main focus right now is to give

him communication and then work on the verbal stuff, because right now he is

not ready to learn how to talk if he ever will be. I would love for someone

who works with deaf children and teaches them how to lip read to work with

him though because he is doing that a little, he may not understand what it

means but he is interested in trying to say what you are and he will look at

my mouth to figure it out, mainly when I am saying mama and dada, just the

basics but with an FM system and some intensive therapy I think he has a

chance, but without the chances are slim to none. Anyway sorry to get all

into this. I will check out that other site.

-- RE: Approved for CCRS

-

PDHH has audiologists on that list that can answer these audiology

questions. Not only are they audiologists - they also have children who are

deaf. I know that one of the audiologists has children with other needs

besides being deaf.

Have your doctors looked into having auditory neuropathy?

Or CAPD?

>

_________________________________________________________________

Get reliable dial-up Internet access now with our limited-time introductory

offer. http://join.msn.com/?page=dept/dialup

All messages posted to this list are private and confidential. Each post is

the intellectual property of the author and therefore subject to copyright

restrictions.

Link to comment
Share on other sites

,

Thanks, I really should join that list, I am a little busy right now though

I have so many e-mails I don't know what is going on with that but when I

finish I will look up your previous e-mail and go to that site.

The doctors have considered AN but the difference between and AN is

that he has a response down to 25 dB in the low frequencies and 30 dB in the

high, which is not consistant with AN but very very similar to it. CAPD has

been ruled out because it is much more severe and there are physical things

that are causing his inability to understand the sound, but they aren't sure

that he doesn't have pure word deafness which technically is a form of CAPD

but not all CAPD is pure word deafness. I have a problem with giving him

the CAPD label because when doctors, educators, and parents think of it,

they think of a child who has difficulty hearing and understanding things,

being worse in noisy situations, but doesn't even respond to the sound,

so it's not just a matter of him not understanding it, we believe that all

sound, sounds the same so he doesn't respond to it. He does however know

the sound of the TV but won't even respond to his name. He will sometimes

say dada if we make that sound, if he is really focused sometimes I sign and

say mmmmmama and he will say baba, because it looks the same, he coppies E

and makes vowel sounds, but that's it. He is not hearing well at all. So I

am wanting services as HI child because speech therapists have said that

while we should keep working with him on responding to verbal sounds, it is

very unlikely he will ever be a speaker. I just don't want him in a class

where the focus is getting him to talk. I do want them to work on that

though, I don't want them to give up, but my main focus right now is to give

him communication and then work on the verbal stuff, because right now he is

not ready to learn how to talk if he ever will be. I would love for someone

who works with deaf children and teaches them how to lip read to work with

him though because he is doing that a little, he may not understand what it

means but he is interested in trying to say what you are and he will look at

my mouth to figure it out, mainly when I am saying mama and dada, just the

basics but with an FM system and some intensive therapy I think he has a

chance, but without the chances are slim to none. Anyway sorry to get all

into this. I will check out that other site.

-- RE: Approved for CCRS

-

PDHH has audiologists on that list that can answer these audiology

questions. Not only are they audiologists - they also have children who are

deaf. I know that one of the audiologists has children with other needs

besides being deaf.

Have your doctors looked into having auditory neuropathy?

Or CAPD?

>

_________________________________________________________________

Get reliable dial-up Internet access now with our limited-time introductory

offer. http://join.msn.com/?page=dept/dialup

All messages posted to this list are private and confidential. Each post is

the intellectual property of the author and therefore subject to copyright

restrictions.

Link to comment
Share on other sites

,

Thanks, I really should join that list, I am a little busy right now though

I have so many e-mails I don't know what is going on with that but when I

finish I will look up your previous e-mail and go to that site.

The doctors have considered AN but the difference between and AN is

that he has a response down to 25 dB in the low frequencies and 30 dB in the

high, which is not consistant with AN but very very similar to it. CAPD has

been ruled out because it is much more severe and there are physical things

that are causing his inability to understand the sound, but they aren't sure

that he doesn't have pure word deafness which technically is a form of CAPD

but not all CAPD is pure word deafness. I have a problem with giving him

the CAPD label because when doctors, educators, and parents think of it,

they think of a child who has difficulty hearing and understanding things,

being worse in noisy situations, but doesn't even respond to the sound,

so it's not just a matter of him not understanding it, we believe that all

sound, sounds the same so he doesn't respond to it. He does however know

the sound of the TV but won't even respond to his name. He will sometimes

say dada if we make that sound, if he is really focused sometimes I sign and

say mmmmmama and he will say baba, because it looks the same, he coppies E

and makes vowel sounds, but that's it. He is not hearing well at all. So I

am wanting services as HI child because speech therapists have said that

while we should keep working with him on responding to verbal sounds, it is

very unlikely he will ever be a speaker. I just don't want him in a class

where the focus is getting him to talk. I do want them to work on that

though, I don't want them to give up, but my main focus right now is to give

him communication and then work on the verbal stuff, because right now he is

not ready to learn how to talk if he ever will be. I would love for someone

who works with deaf children and teaches them how to lip read to work with

him though because he is doing that a little, he may not understand what it

means but he is interested in trying to say what you are and he will look at

my mouth to figure it out, mainly when I am saying mama and dada, just the

basics but with an FM system and some intensive therapy I think he has a

chance, but without the chances are slim to none. Anyway sorry to get all

into this. I will check out that other site.

-- RE: Approved for CCRS

-

PDHH has audiologists on that list that can answer these audiology

questions. Not only are they audiologists - they also have children who are

deaf. I know that one of the audiologists has children with other needs

besides being deaf.

Have your doctors looked into having auditory neuropathy?

Or CAPD?

>

_________________________________________________________________

Get reliable dial-up Internet access now with our limited-time introductory

offer. http://join.msn.com/?page=dept/dialup

All messages posted to this list are private and confidential. Each post is

the intellectual property of the author and therefore subject to copyright

restrictions.

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