rick48
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If u all take great offense to that..oh well.
Don't take offense, just glad you're not teaching my kids.
If u all take great offense to that..oh well.
Don't take offense, just glad you're not teaching my kids.
Thank you..those records of what happened with the CI and the child before coming to my school arent accessible. I would need a good reason to get access to them and the process is very time consuming. U know how busy being a teacher is especially a teacher who has to modify the lessons to make them visually accessible for deaf/hh children. I have been bringing work home to plan my lessons cuz I dont have enough time in the day to do it all. It is tough so of course, I have priorities as described on my job duties and I have to meet those priorities first even it means bringing them home. My job is not to investigate the reason for the failure of the CIs. I find it funny that so many assumptions were made about me. Wow..
If I get "I dont knows" from the parents or the school's audiologists it either means they dont know themselves or they dont want to share the real reasons.
Many of those people have forgotten that I have put posts of children who have benefitted from their CIs...seems like they dont want me to say anything about those who didnt. It makes me wonder why.
Bullies irritate me!
So are yours, stop making up lies about her.
Because, I know. Look at me, I am deaf and I don't hold it against my parents that I don't get the possibility to hear.
buahahaha. "look at me"... sorry this is the silliest argument so far!!
I don't give damn about what YOU think about YOURSELF.
because I for one if I found out my parents had a chance to make me hear better than THAT (what I have now) and didn't take that chance, I would be mad as hell.
There goes your wonderful theory "because look at me".
Fuzzy
"Speech is not mandatory for communication. Have you been in that oralist box of yours so long that you are trapped in there?"
We all understand that but it is for oral communication which is what we were discussing. Try and keep up with us.
"Why? Do you cite your sources? My statements are based on actual experience in the field of education. I see it on a daily basis. I am directly involved with deaf students. I am directly involved in data collection. I am stating facts gained through many years of experience and education. They do not require citation. It is called sythesized knowledge, something that you are quite obviously lacking in. And of course, you once again resort to personal insults in regard to shel, as well as false assumptions. Keep it up and your manner of attack will result in another thread being closed."
Blah blah blah, more double talk and non-answers. "pay not attention to that man behind the curtain." You cannot cite any facts because you do not have them. All you have is your misguided agenda. Well you better get used to cochlear implants and mainstreaming for they are hear to stay and not going away. More and more kids are being implanted every year and there is absolutely nothing you can do about it.
Funny how you expect everyone else to accept your personal experiences as gospel truth but you discount everyone else's. I have more personal experience with cochlear implants then you ever will and what my wife has forgotten (and that ain't much) you have yet to learn. What exactly qualifies you as an expert in the area of cochlear implants, so far nothing you have cited.
Funny, you should be the last one to complain about personal insults and BTW no thread was closed because of any comment either by me or about me can you say the same?
"Speech is not mandatory for communication. Have you been in that oralist box of yours so long that you are trapped in there?"
We all understand that but it is for oral communication which is what we were discussing. Try and keep up with us.
No we weren't. We were discussing designing a hearing baby and CI. Please try to keep up. You are the only one focused on oral communication, and we all know the reason for that. And I would not be so certain that nothread was ever closed because of yoru comments, and your insulting remarks. Once again, you are speaking without benefit of all the knowledge you need to make such assertions.
"Why? Do you cite your sources? My statements are based on actual experience in the field of education. I see it on a daily basis. I am directly involved with deaf students. I am directly involved in data collection. I am stating facts gained through many years of experience and education. They do not require citation. It is called sythesized knowledge, something that you are quite obviously lacking in. And of course, you once again resort to personal insults in regard to shel, as well as false assumptions. Keep it up and your manner of attack will result in another thread being closed."
Blah blah blah, more double talk and non-answers. "pay not attention to that man behind the curtain." You cannot cite any facts because you do not have them. All you have is your misguided agenda. Well you better get used to cochlear implants and mainstreaming for they are hear to stay and not going away. More and more kids are being implanted every year and there is absolutely nothing you can do about it.
Funny how you expect everyone else to accept your personal experiences as gospel truth but you discount everyone else's. I have more personal experience with cochlear implants then you ever will and what my wife has forgotten (and that ain't much) you have yet to learn. What exactly qualifies you as an expert in the area of cochlear implants, so far nothing you have cited.
When you can match my experience, I will give you credit for it. To date, you have been unable to do so.
Funny, you should be the last one to complain about personal insults and BTW no thread was closed because of any comment either by me or about me can you say the same?
Bullies who are pompous arrogant know-it-alls who believe their way is the only way irritate me even more.
I'll match you one for one anytime.
Why yes, I can say that. You are the one that takes the thread to a place it never goes without your input. You are an instigator, and an ignorant and pompous one at that.
See, this is where you show - again - that you have the wrong idea about CI. One cannot choose the CI over a HA. When a HA works, there's no need for a CI. And the normal procedure is still that a HA has to be used first, and when it's obvious that there's no benefit, THEN a CI can be considered.
So please. READ about CI, instead of just accepting Deaf "facts" about CI....
Where did I state about choosin' the CI over a HA ? HA don't require a knife. CI requires a knife. And, I am against CI because of usin' a knife on a baby or toddler ( still a baby ). And, what's more - there's evidence that the CI patients did mention that the CI don't work to help them to be able to HEAR. I've seen them statin' that in some threads. You can not say that the CI WILL benefit to help. I don't think it ever will.
Was it an option in that (what year?) time?
Did your parents consider it?
No, my old doctor recommended them to use HA and sent me to a private school to learn how to talk. My parents don't know what to do at that time when they discovered that I was deaf. When I reached the age of 11 years old, my old speech therapist told my parents that I was close enough to become HoH. I was only 11 years old ! Can you imagine that ? I was wearin' HAs ( both ears ) for 8 years. If, I continue wearin' them, then I will become HoH at the age of 21 for sure. That HAs worked and soo much better than CI since I don't like the idea of usin' knife and carvin' up on the baby's head at that tender age. My head is still good and healthy without touchin' nerves. I don't need complications and that will save my parents from heartaches.
SO, you mean it's in the childs interest to learn ASL, so that it can communicate with less than 0.02% of the people that actually do speak the language. It will have a hard time communicating with the other 99.8% that does not speak ASL....
And this is good for the child - because???
Yeah, why not ? And, no I don't think it will have a hard time communicatin' with the other 99.8% that does not speak ASL. All the USA knew about Gally, right ? Gally is a famous college. Many of them are usin' ASL and they supported it as their first language.
And about "Why put CI first before language ?".... you still don't get it... CI allows the child to have a language... Just like ASL.
How is that so ? Care to elborate it ?
Parents that choose for CI for their child, make the choice that the child will grow up with a language. And not a language that is only visual but cannot be written, but a language that can be spoken, written and cued.
If, you believe that.... can you show me a link with a video ? Show me a deaf child with CI and that he/or she can sign, speak and write. I want you to prove it to me. I want to see it with my own eyes.
And - here's the scary part....
Some parents will also use signlanguage with these children...
Scary.... Children with CI that can hear, speak AND sign....
Have you ever thought that possible...????
Now, please... have a look beyond "deafness only"..
In whose judgement is it as good as nothing? Especially in the case of infants, it is impossible to predict how well a child will be able to use that residual hearing until they have reached certain developmental stages,
and that requires chronological advances.
You can have 2 profoundly deaf individuals who test out to the same degree of residual hearing.....one is able to learn to use that residual hearing through HA and develops speech and listening skills.
If you implant a child at the age of six months, you do not know that they will not have benefited from HA and AVT.
Shel has no agenda where CI is concerned, other than the effects it has on the education of deaf children. Simply because she points out the negative effects it has had on some of her students doesn't mean that she has a hidden agenda.
Those who are attempting to portray CI as the miracle cure for deafness are the ones with the agenda.
more careful than you are, anyway.Not careful enough.
Hearing aids do not provide the same level of benefit to everyone, and the fact that you would even make such a false statement is indication of your total lack of knowledge onthe subject
Obviously, you are not fluent in ASL. And English can be learned at any time, as well. The second part of your statement is based on an oral/audist philosophy.
Actually, I speak. I'm not deaf.
But my son who is deaf communictes with hearing people all the time. If necessary, he will speak. He can also use pen and paper, text pager, or interpreter. Voice is not necessary.
And I will thank you to keep your sarcastic, insulting remarks regarding non-verbal communication to yourself.
Or I see it pointless. anyway, CAN YOU answer?What about it?
I'm assuming that you are unable to answer the question.
Cloggy:And how do you know a deaf child will not hold it against his parents that he did not get the possibility to hear.?
Maria: Because, I know. Look at me, I am deaf and I don't hold it against my parents that I don't get the possibility to hear.
Your own words, Maria.
"Because I know"?? because you know????
I know because look at me - I am deaf, and...
Fuzzy
Maria is tryíng to explain that her deafness doesn´t bother her because she is happy what she is but you?
Simple answer is:
Maria is tryíng to explain that her deafness doesn´t bother her because she is happy what she is but you?
I will be back to make further posts couple of hours later.
Your own words, Maria.
"Because I know"?? because you know????
I know because look at me - I am deaf, and...
Fuzzy
Who is "refusing".??? If our daughters do not feel the need for sign... who are you to force that upon the child - or parent...Yes, cloggy, refusing to allow a child with impaired auditory function access to language through the visual sense to compensate for the impaired auditory sense, even when aided with CI, is linguistically restricting. Do you understand it now?