Designing A Hearing Baby

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There aren't many audis or ENTs that have a CI either. Yet you trust their knowledge.:dunno:


But I do have CI on my left ear.. for Last 6 years I am thankful that I made a right decision to get one.. and NO im not gonna be an Audism or whatever...
I am in BOTH world! I will hang out with my deaf friends.. and I will hang out with my hearing friends I never denied anyone... Except for anyone who can't respect me for who I am...

I always respect for people who doesnt like ci or anything but if they say something that doesn't make sense! i do correct it. I will always say It failed for SOME and it does NOT FAIL for some!


Wendy
 
yes, but, as a hearing aid user I am unable to keep talking well on the phone cuz I've profound hearing loss.. hearing aids are not very helpful with speech understanding to me

I am sorry that HA doesn´t work on you which it does work on others.

What about CI? Have you thought about this?
 
But I do have CI on my left ear.. for Last 6 years I am thankful that I made a right decision to get one.. and NO im not gonna be an Audism or whatever...
I am in BOTH world! I will hang out with my deaf friends.. and I will hang out with my hearing friends I never denied anyone... Except for anyone who can't respect me for who I am...

I always respect for people who doesnt like ci or anything but if they say something that doesn't make sense! i do correct it. I will always say It failed for SOME and it does NOT FAIL for some!


Wendy

Yes, it does benefit some people, and we all admit that. For those who ar able to use a CI successfully, it is a wonderful piece of technology. I do not disagree with that. But, as you said, it does not benefit all. And the young students who have ben implanted, andhave not been able to use their CI successfully for whatever reason, are the ones that shel works with. Those kids deserve an education as much as anyone. And parents considering a CI also need to know that there are children who are not able to use the CI successfully. They need to see both sides of the story if they are going to make an informed decision for their child.
 
I will allow that my reaction to the fact you weren't wearing your CI was very similar to Audiofuzzy's but then you mentioned the headaches that you were having and all of a sudden I'm thinking you sound like Smithr; well, no wonder this CI isn't working out for you.

I kept wondering why you and smithr and why not me? Does this happen to late deafened? I'd be most interested in hearing from them. Does this happen when you wear the CI or does this happen even when you're not wearing the speech processor and a zillion other questions. I don't think it's good idea to ask you a zillion questions though. I'm not a doctor and your doctor and the audiologist should be the ones asking the questions - not me.

These are some very good questions, deafskeptic, and probably best answered by someone who specializes in biological medicine. It sounds as if there is some sort of allergic reaction or rejection going on, and that would be dependent upon the individual's immune system functioning.
 
*have a cup of Ginger tea and reading the whole posts since my last post of yesterday*

I must say that I am total surprised that flip's question with article are being ignored or skip. :hmm:

Re-read flip's question and article, then share your view on flip's article with us please.

http://www.alldeaf.com/839423-post299.html

flip, I am not surprised after read the article, you provided.


Exactly, Liebling. They can't seem to answer the question. Oh, well. Their not answering is an answer. Says a lot. doesn't it?
 
yes I read that article, but how do I know this is too is not yet another sloppy finding???
how do I know if Dr. Ioannidis was indeed himself such careful and correct in his research?
certain margin for errors is indeed unavoidable in such researches, for reason explained in the article but on the whole we have rules and regulations that we go by which more or less can be trusted.

the graph that Cloggy posted is different in this aspect that it is IMO rather hard to falsify the stats when there is not that many implanted people yet, both children and adults,
that is why I rather feel it can be trusted.


Fuzzy

Actually. statistics are very easily manipulated, and the graphs are based on statistics.
 
Are you saying these children from the graph, implanted with CI, who participated in the study were not real life situation? not real children?

Fuzzy

ps are you saying professionals have no real patients?

No,that's not what she is saying. She is saying that testing performed in a laboratory or controlled situation does not always apply to real life because in real life too many extraneous variables cannot be controlled for.
 
That's because hearing people already have a strong L1 language foundation making learning ASL easier. Imagine if they had no language at an older age? That is what happens to many deaf children when they are deprived of a full access to language and then later being exposed to ASL. Their ASL is not the same as the ones who have been exposed to it since birth. When it comes to reading and writing, the gap is even larger.
We cant allow that to keep happening but yet it still is. *sighs*

BINGO!
 
Im sorry if you misunderstood me... What I was trying to say for examples etc...

Sorry, I do not see that you are trying to say for example but admit that your daughter correct your word and wonder why your hubby didn´t let you know... You said the same thing to your mother as well... They thought they let you do on your own which you can´t correct yourself without anyone´s help/support and then share your example of speak "flavor" when you want to say "fever", but your daughter said that you said "flavor".

MY own 13 yrs old daughter shouldnt be my teacher or speech therapist..

Yes I know. I never say that your daughter have to or should help you. I only said that it´s great that your daughter show and correct your word which mean is she do it voluntarily for you.

My husband and my mom could have helped me out

Yes, they should (it doesn´t mean that they HAVE TO or MUST) but should or could...

BUT I had speech therapy when I was young with HA... These DID NOT BENEFIT HELP ME to hear the words better and clearly, they didn't explained me how to pronounce it or to correct it etc...

Yes I know what you mean. They (speech therapy) help me to correct my speech twice a week at school which is not much. My parents are suppose to correct my speech and spend their time to train with me but they doesn´t. They neglect their time with me... Oh Well... I am good to read everyone´s lips. I can image myself if my parents have their time to train with me then I would of speak like HOH/hearing and then will consider CI myself but I do not have moviate myself enough that´s why I know for the sure that CI is not for me. That´s why I am for the parents who help/support/feed the speech, sounds, etc to their children at early age with HA or CI. (depend on children either HA nor CI works on them) and also work together with Audogist how to help the child.

Now, I got CI in my Left ear.. I pick up many words without looking at anyone's lip I can hear words but No one correct my own words! I have been hearing lots of rhymes, or a words that look alike but pronounce almost the same...

so I insulted back to my family (not my kids) that they didnt do for last 6 years with me till Last year my daughter correct me *about 1 year ago* the more I learn and pronounce it myself, and when I read books with my little son I learn to hear my sounds when I talk to everett and kayla would tell me i did good or my husband too.. I do appericate that they did helped me

You said that you had CI for 6 years and pick many words without look at anyone´s lips - nobody correct your word until last year then your daughter correct you... Correct? I want to make sure either I understand you correct or not.

Yes, like what I said before that it´s great that your family helped you voluntarily.




I am ALMOST 40 years old! next month.... But my brain level is just like a 2 or 3 years old child with hearing words! so I will have to write down words on what I hear without looking etc... (that's my guess on age's level for words concept knowing without looking or reading)
For anyone in this Alldeaf--
Im saying that.. CI do benefit for many children if they done in early ages... not at Later ages... HEY i said Many children i didnt said ALL children so Some of them may not success.. It's like Fuzzy says

to anybody in AD--
Someone asked me the risk of doing another ear, if I done another ear surgery, in about 10 or 20 years later there's new technology come out but may not work for me anymore cuz I got implanted in both ear(IF that happen), then I told him, Look, I will be 40 next month, I dont even want to wait any longer for another 10 or 20 years because I will be too old to LEARN allover again.. I would rather get it done now, If it failed on my right ear, then i accept the risk, but if it work, I will be happy to work along with my children, and my family...

My family support me to get ANOTHER CI on my right ear.. that's why I went for the evaluations yesterday!

Wendy

I will answer part of your post later because we have an appointment with Bank today.
 
Exactly, Liebling. They can't seem to answer the question. Oh, well. Their not answering is an answer. Says a lot. doesn't it?

As to the article itself, since you are always mentioning but never citing research and studies, surprised that you have not responded. Since I favor personal observations and experiences over studies and research, no comment is necessary from this corner but in any event R2D2's response however said it best.

As to his "curious observation" about the educational levels of oralists, guess since none of them have responded to it, it goes to show you that they are intelligent enough not to respond to such an idiotic observation.

But since you are wondering why there are no responses to a foolish question, wonder what that makes you?
 
As to the article itself, since you are always mentioning but never citing research and studies, surprised that you have not responded. Since I favor personal observations and experiences over studies and research, no comment is necessary from this corner but in any event R2D2's response however said it best.
That was my point, thanks for supporting it.
 
Originally Posted by Audiofuzzy
As I've said- I am only stating facts about CI - how do you know what would happen if you could wear it everyday? that has nothing to do with your unfortunate symptoms, or family.

The facts is not always correct.

Now Liebling let's not go crazy with the "facts not correct" theme because of Flip's article, OK? :)
just because something is a "fact" does not mean it is suspicious on principle.

It's one thing to be wary of a few million scientific studies another to say "it's a fact the sun is bright". or are you going to argue now that the sun being bright is not correct fact, too?

I said: turns out Puyo couldn't wear CI. So Puyo couldn't exercise, exercise, exercise hearing with CI. remember what the other poster said: "I am 40 but my brain is like 2- 3 year old, I have to learn how to hear with CI" ??

That is why I said maybe if Puyo was not having problems with his mouth and headaches, THEN maybe he would use CI more and more, and more, and with time he, too, could learn how to hear over the phone.
we won't know it because he can't use CI. but it's possible it WOULD be better.
that is why I said Puyo don't know if the CI would work better for him or not because he can't spend more time on it. he only spend 4 months wearing it. not Puyo fault.




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That have completely NOTHING to do with what I wrote. I was writing about human speech and language development, not you.

Do I understand correct that you beleive that CI is the one who develop human's speech and language, not people themselves?

Yes, but you have to first learn to separate many layers surrounding speech and language development.
You must separate them,and dicuss them separately or we will never clear this up.
From biological point of view, human brain is NOT finished developing AFTER birth. I mean the body of the brain (in the head) is done, but the processes that happen inside the brain are not.

When the baby is born, the brain is making neural pathways connections, thus is developing.
this happens regardless of any parental intervention, it is just a part of human development.


BUT

the brain will develop as much as much it receives stimuli from the outside.
the more stimuli, the more developed brain. to develop ability to hear and speak you need to hear sounds, and so you repeat what you hear, and thus develop speech.

This is when the CI and parents enter.

Without ability to hear, no matter what will the parents do the deaf baby will not hear, and the baby's brain will not make neural connections.
After the age of three the making of these connections slow down and eventually stop. No matter how much stimuli AFTER that age - the brain is mostly finished making connections. It won't learn much anymore. It will some but never as much as before age of three.

If the deaf baby is implanted with CI, then the baby can hear.

If the baby is implanted before the age of three, the brain will make as many connections as the baby will hear sounds from the outside - because the brain is still in the actively developing mode.
Now, if the baby will only be implanted with CI but not be exposed to sounds - then the baby will hear some but not as much as the baby who will spend a lot of time in hearing therapy.

If the deaf baby will not have CI, or only HA before the age of 3, then the baby will not hear antyhing or only as much as HA allows. Thus no matter how much parents will work the baby's brain will not be developing as much sounds as in the baby with CI.

That is why it is important to understand first the process of human development from purely biological point of view, before start mixing it with raising a baby.

Do you understand me now?




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It doesn't matter what situation - it is always the attitude and communication skills that play the role in relationship. If my son was sure this is what he needs and decided to change his gender, I would respect it.


*scratch my head* -

You support parent's decision on CI surgery for their children but you said different here... You said that you respect if your son decided to change his gender...



The gender changing surgery is not done for under 18 years old anyway. Unless it's medical matter requiring immediate decision.
besides this is completely different situation - it has nothing to do with brain developing senses before age of 3.. and anyway I only was asked "what would I do if". I support both in those cases.



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I am sorry, but what are you talking about? I am talking about people who had NO USE for HA, but can now hear with CI.

I am sorry that you still can't get it and can't convince it.

I am sorry but I don't get you. I am saying some deaf people can not hear with HA because their hearing loss is too great. But they can hear with CI (if implanted).




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CI is more advanced technologically than HA, period. It has nothing to do with parent's support and willingness to work.

Disagree and would suggest you to RE-READ WHarley's post. Without parental or family's support, CI or HA users know nothing... what kind of noise/sound is about... they don't know either their speech is correct or not... ????


Again, you must separate the subject of discussion because I am confused - what are you discussing, exactly? the technological POV or practical POV?
I was talking about technology. Only.
From technological POV the simplest CI is way more advanced than most advanced HA. because HA can only amplify sounds while the CI does more than that.
From practical POV of course just putting either CI or HA in there is not enough to have benefits.


CI and HA only help if the people are willing to learn anything with their development skill.

Correct, but also don't forget about human development from biological POV.


I know that CI is better techology but really depend on people's physical body and mind either it work on them or not.

Oh, I see you do know that :)



Don't confuse two things: language development and ability to hear and speak.


I can see that you has a little knowledge.

?????



Many hearing children of deaf parents have their delay with their speech development until they start their first kindergarten and catch it real fast.

Correct, but again from "biological" POV they do hear every sound that surrounds them. Just because their parents are deaf are unable to speak doesn't mean they do not produce ANY sounds. On the contrary deaf people can be very noisy - they watch TV loud, they move about making a lot of sounds, majority of deaf people do have some ability to speak so they do communciate verbally with their babies (googoo, coo etc) and so on.
the baby hears all that, and also if you take your baby anywhere - shopping, playground, doctor's office -anywhere - the baby IS exposed to sound.
so the conenctions in the brain DO happen, just not in as optimal way as of the baby's with hearing parents. and like you say they catch up later well. I knew that.

My both children grow up at deaf world more than hearing world. Sign language are their first language.

I have seen that happen many times, and without exception all the children were able to develop speech.

I accept that my both boys are hearing and want them to join hearing world, that's why CPS send my boys to child minder with their cost to develop their speech skill until they went their first kindergarten when they were 3 years old.

That is great! you are a great parent.


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because they COULD HEAR. it only matters when the child is born deaf, not when the parents are deaf.

Can hear what? Just can hear?


As you probably read about human development by now, I would say yes just hearing is what matter most. any sounds.



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I also don't understand why nobody is getting the clue from this:

I do not understand why nobody accept CI and HA users's experience in real life and depend on studies, professionals, books, etc. instead of both sides.

No, I do accept all, it's just I like to have explanation why something is not working as it should. was it because the child was born deaf and implanted past the age of three? was it because it was implanted before the age of three but not taught speech and sounds immediately? was the hearing loss more pronounced than it was first thought? was the adult implantee willing to work as hard as it is needed? was the body rejecting implant? is the hearing loss type not right for the CI? etc.
Not every implanted person is well infomed about all this. For example, some people didn't knew it will be so much hard work to learn to hear.
Some don't understand the importance of early implantation.

Exactly, it's parents who feed the language and speech skill to their children with the help from HA or CI, not HA or CI itself.

Correct, but if the child can't hear all the parental work in the world won't help. One depends on the other.

Fuzzy
 
I know some people don't beleive that HA users, I withnessed in my real life can speak like HOH/hearing and can talk on the phone...

See yourself that I am not only one who said this...

http://www.alldeaf.com/556123-post18.html

I don't think anyone here disputes that. It depends on the severity of your hearing loss. If you have a moderate to severe loss then yes, it's possible for such HA users to use the phone. But such people don't qualify for CIs anyway and will find it hard to get one.

If you have a profound loss however, HAs usefulness declines significantly and CIs begin to have the edge in terms of clarity. It's not common for profound HA users to be able to use the phone. With my HAs I could not use the phone because my loss was just too big, but with my CI, I now can.

Anyway, just about every child and adult who goes through the process for a CI is required to trial hearing aids first, unless they are so obviously completely deaf. I tried out two different hearing aids before I had my last operation. With my first CI, I was made to put on my hearing aid for the test, even though it was really painful for me to wear it due to recruitment. We are then tested for speech discrimination with our hearing aids on. If a person does well with hearing aids then he or she will not qualify for a CI.
Insurance companies and governments do not want to shell out money for CIs for people who don't need them.
 
Exactly, Liebling. They can't seem to answer the question. Oh, well. Their not answering is an answer. Says a lot. doesn't it?

Perhaps you missed my response?
 
Take a course in research methods. Perhaps then you will be able to use some analytical skills when you try to understand the research you attempt to read.



That's just Jilliospeak for I have no counter argument so rather than admit you are right, I'll just insult you.

Taken the research methods course as well as 4 or 5 courses on statistics.

Please tell us how sign language skills are relevent to a test of whether a deaf person with a cochlear implant can hear someone speaking bisyllabic words WITHOUT any visual clues?
 
The fact that kids with CI still need speech therapy tells me that CI doesn't give perfect hearing. I don't have CI but I do have first hand experiences with speech therapy with sign language and without sign language. I get more done in speech therapy with sign language.

Or could it be that since the first time of a childs life, hearing is very important in order to develop speech. Starting to hear will delay that phase for 1 to 3 years, so speech therapy is used to catch up...

After all, people that became deaf later in life and used CI speak without any problems...... According to your thinking, that indicates that "CI gives perfect hearing".....
 
.............
Let me to share an example:
Your daughter and other child have same level of hearing loss and have CI at early age. Your daughter's learning development skill is quickly than other child. How? Can you explain me why your daughter and other child are different? Where it come from?
Of course there's a difference with every child. And Lotte might be doing very well, or she might be average, or lacking.

BUT, in a study like the one I showed, there kind of differences would be averaged out. Because, the same as you suggest for Lotte and another child is valid for the children in the other columns. Over there there are also children that are doing great with their CI, and some that perform below that.

The graphs show the avarage performance. And THAT shows a gignificant difference between early implantation, and later..
 
Actually. statistics are very easily manipulated, and the graphs are based on statistics.

True. It's easy to lie with statistics. That does not mean all statistics lie.
Then again, it's also easy to show real differences with statistics.
And, when the differences are this big, like in the graph I showed, it can hardly be due to statistics. It is due to the results...

And again, it's interesting that when an article shows something YOU don't like, you bring up "statistics are very easily manipulated".... Without any foundation as to why the article / statistics could be wrong... It's just a cheap shot at an article you don't like
I haven't seen you questioning statistics you have brought up...

Let's face it. The article clearly shows the benefit of early implantation. YOU might not like it, but there it is.

But for parents of a deaf child, the first first decision they have to make for their child is to have the child grow up with - or without sound.
If the decision is to have it grow up with sound, research like this is helping them in making the decision about WHEN to implant...
 
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