Hear Again
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If they are doing speech it is not AVT.
Yes, it is since speech therapy is a component of AVT.
Let's agree to disagree faire_jour, shall we?
If they are doing speech it is not AVT.
We're talking about covering a mouth for minutes a day, if even that.
I can't speak for everyone, but I assume most everyone who wears a HA or CI in this forum wears these devices so we can hear words and sounds (why else would we wear our aids or CIs? For the sheer experience of wearing something in our ears and getting no benefit from it?)
And, for many of us, we get additional benefit out of our HAs and/or CIs when we've "worked" to learn to distinguish between sounds and words -- look at all the word and sentence discrimination posts in AllDeaf. Covering a mouth for minutes in therapy helps train a child's ears, so they'll understand even better, even with lipreading.
So did I.
I don't know anyone who walks around with their hand covering their mouth, but they do talk from the other room, behind the child and far away, in ways that the child can't lipread, instead of coming close and letting the child lipread.
Alot of people talk with their hand covering their mouth. Just ask ADers here. I'm sure many of them could share experiences where this has happened to them. I know it has certainly happened to me. (I can tell this by the muffled sound of their voice.)
I mean AV parents, walking around with their hands covering their mouths to prevent lipreading. I have never met one who does that. And in our therapy sessions we use an "acoustic hoop" so thst the sound isn't effected but the mouth is still covered.
In AVT sessions, it's typical to use a hoop, so that isn't unusual at all.
How do you know parents who have their children in AVT don't walk around covering their mouths? I'm sure some of them do.
Besides, isn't that the whole point of AVT?
I know them, my child plays with them, I am involves in organazations with them. I see them interacting with their children. I would say I had 100 families at my last Hands and Voices activity and at least half of them do AVT and I didn't see the hand cue once.
You literally were able to observe 50 families and how they communicated with their children? Wow. You have amazing eyesight.
Having said that, just because 50 families did not use hand cues doesn't mean other families don't.
Besides, how do you know what the majority of AVT parents do or don't do?
Are you in their homes 24 hours a day?
My job is to greet and interact with them, so I try to spend time with each family. I can only speak to my experieces, and I don't know anyone who does.
Bringing hearing to normal or near normal levels does not solve the problem of distortion and lack of clarity.
All the AVT in the world won't help a person who cannot discriminate speech due to lack of clarity.
As for trying out hearing aids, how far do you want people to go? Do you really expect someone to try every single high powered hearing aid on the market before receiving a CI?
I find it ironic how the 2 people who suggest this (deafdude and DD) are happy with hearing environmental sounds and have decent enough hearing with hearing aids to understand most speech.
Really? You can hear the "th" sound? How about "f"? Those are at about 15 db at 4000 hz. I dare you to find a hearing aid that can bring a profound loss at 4000 hz up to 15 db. If you are happy with enviromental sounds, Hurray for you! I wasn't ok with that for my kid. Why stick with something VASTLY inferior when there is a BETTER option? CI's bring better high frequency hearing, improved clarity (so improved that my daughter didn't even realize it hearing, she didn't label it as hearing right away), and speech understanding, not just recognition for many who couldn't get it with hearing aids. WHY NOT?? I just don't get the reason to cling to a technology that isn't helping.
AVT would be nearly impossible with a severe-profoundly deaf hearing aid user. It would be cruel for a child. How can you learn to listen when you can't hear?
I think the reason why AVT is given to CI recipients is because there is more hearing to work with. Since a person is able to hear (generally) between 20 and 30 dB, it makes sense that they would be trained in regards to being able to hear/understand speech, use lipreading cues as well as identify sounds.
Agreed.
Faire_jour and Hear Again,
I'm aware that there are FDA reccomended guidelines for implantation.
However, that doesn't mean there isn't "off label" implantation going on for folks who are borderline. Matter of fact, with the current state of health care costs in the US, it would surprise me if this wasn't happening! You know.....high insurance premiums PLUS the out of pocket costs for hearing aids. I do know of two boys who could hear in the high 60ish percentages aided getting implanted.
If I recall correctly the mom got them implanted b/c unaided they could only hear 10% unaided.
Yes, hearing in the high sixites isn't perfect, but it's a lot more then the little to no benifit from HA that CI folks claim is needed for implantation.
I mean it wasn't like they were hearing in say the low 30 percents with amplification. Up to or around 45% WITH amplification, I think should be implanted without a huge hassle. That's like a hoh person upgrading from ITE aids to BTEs.
"Off label" use of the CI is being seen. Yes, it prolly would be impossible to get it for a unilateral profound loss or whatever. And I do think that the majority of implantees opt for it after a long hard period of decision.
But there's the fact that some of the marketing practices about CI haven't been exactly kosher. (ie "comissions to audis for referring clients to CIs, stuff like random people IMing potentional CI implantees and telling them they should get a CI)
I know how you feel about CIs and "borderline" candidates DD -- although I agree with faire_jour that either you are a CI candidate or you're not. There are no two ways about it.
Besides, if the mother you mentioned wanted to have her child implanted and the surgeon agreed, what's so wrong about that? He could be hearing at 15-20 dB across all frequencies and have 90% speech discrimination or better.
By the way, did that child you mentioned have a progressive hearing loss? If he did, that probably explains why he was accepted as a CI candidate.
Despite what those qualifications say, CI candidacy criteria vary from one CI center to another. I know some CI recipients who had severe-profound hearing loss and were denied candidacy because the CI center they were evaluated at only implants those who have profound hearing loss.