CI facts page... FDA

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dreamchaser

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There are a lot of interesting tid bits on the FDA's website on CIs. They are worth reading. just go to FDA, and then type in cochlear implants. There is a short animation of the surgery and a list of about 30 Risks, and the few benefits... Interesting yes, but important to know if you are considering an implant.

Keep in mind when reading this: The FDA is heavily lobbyed by the Imlant industry and the oralist only activists, so they are always being pushed to continue to lower the age for an infant implant. They do list the Risks, but they don't emphasize them enough.
 
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The FDA is heavily lobbyed by the Imlant industry and the oralist only activists
Good point............the implant industry and AG Bad and that Oral Deaf Education Foundation really does have quite a bit of money to push around. I don't think that it's "oh it's totally bad and they're trying to make it seem 100% good and decent.".....but I do think somewhat that there is lobbiest (pro oral b/c after all, ASL and Deaf culture doesn't make anyone money) influence.
 
Oh and how about listing ALL the risks and the "few" benifits?
Lots of people here would say that the CI has definitly benifited their lives.
I mean, even if you're mostly anti-CI you gotta admit that it's been great for people with severe tintitas, and recruitment. As well as for people who are straight right off the bat canidates (ie NO benifit from HA) . I do think they should be a little pickier when it comes to ambigious canidates. That's just my feeling.
 
Keep in mind when reading this: The FDA is heavily lobbyed by the Imlant industry and the oralist only activists, so they are always being pushed to continue to lower the age for an infant implant.


Source of this information?



.
 
Oh and how about listing ALL the risks and the "few" benifits?
Lots of people here would say that the CI has definitly benifited their lives.
I mean, even if you're mostly anti-CI you gotta admit that it's been great for people with severe tintitas, and recruitment. As well as for people who are straight right off the bat canidates (ie NO benifit from HA) . I do think they should be a little pickier when it comes to ambigious canidates. That's just my feeling.

I mostly think that it is a preference for anyone that is willing to take the risk because their desire to hear is very strong. I think that many hearies just assume that implants can fix everything and that hearing will be normal with an implant. There are a lot of misconceptions out here. People are ignorant because they really get more information about the good experiences and no info on the bad experiences.

Mostly, I just want people to get as much information on the health risks as they can before they make a commitment. It is easy to change your mind about a hearing aid if it is annoying you or causing problems, or if it just doesn't work. But if you are unhappy with your results of an implant you have to endure another surgery to get rid of it. So,, just want people to be aware.

I am not anti CI,, I am a little concerned about implanting babies. The age just keeps getting younger. ???? I aint no expert. Just hoping people get good information from other people than the CI industry.
 
I mostly think that it is a preference for anyone that is willing to take the risk because their desire to hear is very strong. I think that many hearies just assume that implants can fix everything and that hearing will be normal with an implant. There are a lot of misconceptions out here. People are ignorant because they really get more information about the good experiences and no info on the bad experiences.

What and where are the lots of misconceptions your speaking of?



.
 
What and where are the lots of misconceptions your speaking of?



.

Howdy, One misconception I was referring to was that many hearies I know assume that an implant will produce *normal* hearing. They think that they are vetted, safe, tried and true miracle cures that work 100 % for every Deaf person the same, and they don't understand why all Deaf people can't just stand in line and get fixed. they are not aware that there are other problems that can be associated with implants and that there are some health risks to consider. OF course I have not spoken to Everybody about this, but I have heard this attitude reflected in such a majority of people, that I would think it is a common misconception. Before I started to research CI's, I thought the same thing. I must not have been very clear. I realize my posts don't usually come out to say what I meant the first time through.. Sorry... :)
 
Source of this information?



.

I will have to get back to you on the sources I quoted when I did my research paper. I have it stuck away somewhere. Are you telling me that the CI industry does not lobby the FDA to approve early implantation? That could be. Maybe I didn't dig deep enough to find the other side. I just didn't run across any articles that said, FDA doesn't hear requests from the CI industry to lower age for implantation of infants. I will try to dig up my documentation for you and establish a little ethos. The main point I was trying to make here was that I was very unaware that there were any health hazards with implantation. I didn't realize that they kill residual hearing. I was not aware that it is possible to end up with a paralyzed face if the nerve is nicked. The only stories I had ever heard were the success stories, so I naturaly assumed that all implants were successful, when the truth is that some implants cause absolutely no change in hearing, and some only bring a small change. There were many things that I was not aware of before I did some research for my paper, which by no means makes me an expert on implants... And believe me,,, for every successful implant I am thankful to God that the technology helped someone. I am thrilled for them. I am currently praying for a few people who are having the surgery soon to have a successful and safe experience. I want them to be able to hear if possible, but I don't think that they should feel that they have to get an implant for any other reason than that is what they desire more than anything, because there are things that can go wrong. Have a wonderful night, I will look for that info tomorrow. :) Jeanie... still chasin the dream for a better tomorrow for ALL!
 
. The main point I was trying to make here was that I was very unaware that there were any health hazards with implantation. I didn't realize that they kill residual hearing.

I will have some residual hearing. My doctor discussed this with me. I knew of the risk. I did not have must residual hearing so I was not concern.

I was not aware that it is possible to end up with a paralyzed face if the nerve is nicked.

I knew of this risk. That is why the nerve is monitored during surgery. I had a benefit, since my facial nerve is damaged from the birth of daughter. The facial nerve stimulator increased the degree that I feel on my left side. Now I do not have as much facial numbness.
 
The only stories I had ever heard were the success stories, so I naturaly assumed that all implants were successful, when the truth is that some implants cause absolutely no change in hearing, and some only bring a small change.

There are success stories so don't dismiss them. Mine is a success story. The biggesst myth is that CI users are not told the risk and benefits. I have been. My doctor is at the cutting edge of CI surgery. I spent a long time throughout a year discusssing the risk. Now I am enjoying the benefit.

There were many things that I was not aware of before I did some research for my paper, which by no means makes me an expert on implants...

It does not make me an expert either, just someone who has been throught it with BOTH ears. I call it experience. !![/QUOTE]
 
I will have to get back to you on the sources I quoted when I did my research paper. I have it stuck away somewhere. Are you telling me that the CI industry does not lobby the FDA to approve early implantation? That could be. Maybe I didn't dig deep enough to find the other side. I just didn't run across any articles that said, FDA doesn't hear requests from the CI industry to lower age for implantation of infants. I will try to dig up my documentation for you and establish a little ethos. The main point I was trying to make here was that I was very unaware that there were any health hazards with implantation. I didn't realize that they kill residual hearing. I was not aware that it is possible to end up with a paralyzed face if the nerve is nicked. The only stories I had ever heard were the success stories, so I naturaly assumed that all implants were successful, when the truth is that some implants cause absolutely no change in hearing, and some only bring a small change. There were many things that I was not aware of before I did some research for my paper, which by no means makes me an expert on implants... And believe me,,, for every successful implant I am thankful to God that the technology helped someone. I am thrilled for them. I am currently praying for a few people who are having the surgery soon to have a successful and safe experience. I want them to be able to hear if possible, but I don't think that they should feel that they have to get an implant for any other reason than that is what they desire more than anything, because there are things that can go wrong. Have a wonderful night, I will look for that info tomorrow. :) Jeanie... still chasin the dream for a better tomorrow for ALL!

Actually, even though the age limit is 12 months according to the FDA, individual CI surgeons can petition the FDA to have that limitation waived so that implantation can be done at earlier ages. Physicians are petitioned by CI manufacturers to use their particular devise.
 
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The only stories I had ever heard were the success stories, so I naturaly assumed that all implants were successful, when the truth is that some implants cause absolutely no change in hearing, and some only bring a small change.

There are success stories so don't dismiss them. Mine is a success story. The biggesst myth is that CI users are not told the risk and benefits. I have been. My doctor is at the cutting edge of CI surgery. I spent a long time throughout a year discusssing the risk. Now I am enjoying the benefit.

There were many things that I was not aware of before I did some research for my paper, which by no means makes me an expert on implants...

It does not make me an expert either, just someone who has been throught it with BOTH ears. I call it experience. !!
[/QUOTE]

Yes, there are success stories, and within those stories, there is a great degree of variance in success. Not all "sucesses" are identical in ability or benefit provided, and it is very dependent upon the way in which success is operationally defined. That said, of course there are successes, and no one has ever said there aren't.

However, there are also failures, and less than successful implantations. Those need to be recognized as well in order to have a complete understanding.
 
Yes, there are success stories, and within those stories, there is a great degree of variance in success. Not all "sucesses" are identical in ability or benefit provided, and it is very dependent upon the way in which success is operationally defined. That said, of course there are successes, and no one has ever said there aren't.

However, there are also failures, and less than successful implantations. Those need to be recognized as well in order to have a complete understanding.[/QUOTE]


No, all successes in any area are indentical. Not all successes with hearing aids are identical nor with CIs. But yes my CI are my own personal success. Do not disregard my experience with them or disregard families experiences with them. What I am finding out are expectations for success, some CI users want normal hearing. That is not going to happen. My doctor said it. He also told me that music would take years if any for me to enjoy. I am enjoying music daily. It is all about expectations, experience and enjoyment. I have all three with CI and no enjoyment with ha.
 
Yes, there are success stories, and within those stories, there is a great degree of variance in success. Not all "sucesses" are identical in ability or benefit provided, and it is very dependent upon the way in which success is operationally defined. That said, of course there are successes, and no one has ever said there aren't.

However, there are also failures, and less than successful implantations. Those need to be recognized as well in order to have a complete understanding.


No, all successes in any area are indentical. Not all successes with hearing aids are identical nor with CIs. But yes my CI are my own personal success. Do not disregard my experience with them or disregard families experiences with them. What I am finding out are expectations for success, some CI users want normal hearing. That is not going to happen. My doctor said it. He also told me that music would take years if any for me to enjoy. I am enjoying music daily. It is all about expectations, experience and enjoyment. I have all three with CI and no enjoyment with ha.[/QUOTE]

I don't think that anyone is disregarding your success, vallee.
 
Please forgive me if I made you feel that I negate your success!

I sometimes can't keep up with my own thoughts and type what I mean without losing the flow that connects my thoughts,,, Of this I am guilty.

If I somehow did not make it clear that my intention for posting this info was to be sure that everyone got comprehensive information about a very serious and usually permanent decision. If I didn't make that clear, then I humbly ask your forgiveness.

As I thought I stated earlier, I am not at all against CI's for anyone who has made an informed decision. For every success story I am thankful and excited. I am thankful for every technology that bettered the quality of life for anybody. I am not against prosthetics of any kind if they help. I am not against interpreters, or any other system or tool that people find that works for them to enhance communication. Please, I can tell you truly, If I could give you hearing, I would sacrifice all that I ever hope to attain to do just that. I have enjoyed sound all of my life, and now that I am nearing the end of my life, I would probably give you my one of my own ears if that were possible. I would always have my memories of sound, and I would have ASL to communicate with. Why not pass on that blessing? Unfortunately, I don't think that is a possiblility, but I would be willing. You can think I am full of crap if you want, but you can't know the sincerity of my heart and my desire to eradicate another person's pain.

I have decided to share a short story with you that I wrote.
I have not posted this story for many reasons, but mostly because I fear it may not be good enough, or it may sound condescending. It is not meant to be at all a form of kissing ass in the Deaf community. It was written in an attempt to reach hearies with a different insight into the Deaf community. It may even sound controversial, but I am gonna post it now in the hopes that you will get it that my intentions are not to hurt anyone, but to encourage people to be informed. My goal is to be bridge between the hearies and the Deafies through educating hearing people about the unfairness that Deaf people endure in the school systems and in the job market etc. It is not to eradicate technology. If you only knew how much I care that your world is a happy world, then you may understand my willingness to stick my neck out and try to get involved. Mostly I am trying to be as educated about your lives and your needs as possible, and then to relate that back to the hearing world. I have a deaf granddaughter that will one day enter school. She is only four months old right now. She is also blind due to a nodule imbedded in her brain that is pressing on the part of the brain that she needs to use her senses. I don't understand all of the medical garbage yet, but I do understand that I love her, and I want her to belong to a culture where she is accepted, nurtured and educated without prejiduce. I also care that the quality of education she gets is sufficient to help her reach her potential and to be an asset to society. I hope this story will give you insight into me. It is still in a rather rough form.

OK, I lied! I don't know how to add attatchment here, but if you would like to read it, pm me and I will send you a copy. I only takes about ten minutes or less to read.
 
The only stories I had ever heard were the success stories, so I naturaly assumed that all implants were successful, when the truth is that some implants cause absolutely no change in hearing, and some only bring a small change.

There are success stories so don't dismiss them. Mine is a success story. The biggesst myth is that CI users are not told the risk and benefits. I have been. My doctor is at the cutting edge of CI surgery. I spent a long time throughout a year discusssing the risk. Now I am enjoying the benefit.

There were many things that I was not aware of before I did some research for my paper, which by no means makes me an expert on implants...

It does not make me an expert either, just someone who has been throught it with BOTH ears. I call it experience. !!
[/QUOTE]

HI Vallee, I hope that you will take the time to pm me so I can send a copy of the story I wrote. Maybe it will let you know more about me.

I am so glad for you and your successful implant. I used to write songs and sing and play guitar, so music has a big place in my heart, and I am so glad that you are experiencing it. Just as a curiosity thing, not because I am trying to argue against implants, I wonder how it sounds to you. Do all of the sounds come through on different ranges? I mean do they blend together or sound separate? I so hope that you can enjoy the full magic of music. I also hope you can enjoy ASL music. I love the signed music at my church.

I don't if the technology has improved a lot since I did my research paper (23 pages of documented stuff).

Is there any financial assistance out there to help you to keep up with the cost of batteries? If not, maybe someone should look into establishing a foundation that deals with those kinds of needs.

Did you happen to read the FDA site? IF you find things there that you think are untrue, then please let me know.

I hear that there are other new technologies that are being researched right now that may help to restore normal hearing. If it becomes available, are your nerves still in tact enough to benefit from nerve regeneration? Geeez, so much I want to know. I am glad that you took a year to ponder your decision and get informed. It is always wise to vet things when your health is involved. I could not find any long term data though about long term affects of electrical stimulation in the crania. Do you know where I could find some of that info?

Well, I wish you all of the success an happiness in the world. Maybe you could keep me informed of your progress in the future and dispell some of my fears? :)
 
What and where are the lots of misconceptions your speaking of?



.


Hey Bill, how ya doin this fine day... LOL,, we just had a hail storm and snow. That never happens this time of year here.

I think I addressed the misconceptions that I was referring to, but you also asked for documentation concerning the fact that I believe that the implant industry has not compiled a list of people who have expereinced a problem due to implant surgery.

It is also hard to find statistics on the amount of people who have chosen to have one removed due to the relentless noises in their head or infection or equipment failure. This information is pretty much protected by the medical privacy laws.

I have not found a CI site that discusses how many people have failed to benefit from an implant, or the NOT successful stories. I have also not heard them address the oral-only controversy. They leave that up to the oralist to do. I do believe that I had an article saved that said that the oralists have actually partnered with the audiology industry to lobby for earlier implantation. As a general rule the age limit is 12 months, but we do know that imlants have been authorized at even younger ages. Logic would dictate that the FDA did not lobby themselves on this issue, and it was not a God-given inspiration that made them authorize earlier implantation. So, I assume that what I heard was true; the CI industry and the oralists lobby the FDA.

I feel hurt that you would think that I would rob a child of their right to hear. I understand that you are adamant about implanting your own child and that you think you made a good decision for him/her. I pray to God that you experience nothing but the best from your decision and that your child grows to have a full life and reach his potential.

I understand that the oralists and some other researchers believe that early aquisition of sound will encourage language development better; thus, we must implant babies as soon as the screening shows a hearing loss of any sort. Is there an age limit that you feel is appropriate? Should they automatically implant children who are HOH, or only deaf in one ear? How much hearing loss must a child display before he is automatically wheeled off to surgery so he won't be a drag on society? I am truly curious to see where you think the line should be drawn.

Do you have any statistics from a LONG-term data collection that shows the absolute effects of sending electrical impulses into someones head? A whole lifetime of say, 60 to 100 years of electrical impulses invading the brain has not been documented to my knowledge, but if you have the data, please share.

I am curious. If an implant does not benefit a person or is causing a problem, does state insurance pay for a new surgery to have it removed? Is that saving the tax payers money? I am confused.

Have you heard of human error during and afer surgery in hospitals? Is it not possible that a tiny baby with the smallest of ear canals and nerve system might be accidentally injured during a surgery? Is that terribly hard to concieve of. I realize that the claim is that implants are SAFE. But ya know, they said the same thing about electric shock therapy to cure depression, and the same is true of breast implants and lypo suction. Ya know, they use to promolgate LABOTOMIES too, until someone decided that it was unethical to experiment on people by giving them an irreversible and life-changing operation,, just so they would not be a drain on society.

Can you guarantee me that if we were to seek an operation to remove my granddaughters nodule, with only a slight hope for success, can persoanally guarantee me that she will not contract an untreatable staph infection or flesh eating from the surgery? These germs are mutating faster than we can create medicines to combat them. I know this is true because I just lost my husband from a staph in fection that he contracted in the hospital during a minor back operation. It ate through his spinal cord, and he had a massive stroke that made him brain dead, and on our anniversary, they pulled the plug. Any major invasive surgery can cause death due to the above mentioned complications, a blood clot or any number of reasons.

I want people to hear. But if they can't, I love them just the way they are. They don't need to undergo a painful and unpredictable surgery to accomodate me. I hope this doesn't sound crass, but it is on topic: If your child would have died from a secondary complication, what would you feel...especially if he were not old enough to express his desire or lack of desire to have the surgery inspite of the potential risk to his health?

Did you even read the FDA website??

After you do, please return and lets have a civilized discussion about this. Like I said, at least I care enough to try to be sure that people have access to all of the information available before making such a huge commitment. I was not trying to offend you for your choice, nor am I trying to do that now. I just want to be sure that comprehensive alternatives to the surgery are presented, and the risks are rightly represented. If we are looking for a happy story, the implant industry has already provided lots of glowing accounts for us to access. Unfortunately, I have not yet been able to find their accounts of the not-so-gowing experiences.

You are apparently an intelligent and educated man. You made a decision based on what you believed to be true after you were presented the facts. I am not sure that all hearing parents have done there research as thoroughly as you and I want to encourage to do so. Again, I apologize if my typing does not reprsent my whole thought.
 
Hey Bill, how ya doin this fine day... LOL,, we just had a hail storm and snow. That never happens this time of year here.

I think I addressed the misconceptions that I was referring to, but you also asked for documentation concerning the fact that I believe that the implant industry has not compiled a list of people who have expereinced a problem due to implant surgery.

It is also hard to find statistics on the amount of people who have chosen to have one removed due to the relentless noises in their head or infection or equipment failure. This information is pretty much protected by the medical privacy laws.

I have not found a CI site that discusses how many people have failed to benefit from an implant, or the NOT successful stories. I have also not heard them address the oral-only controversy. They leave that up to the oralist to do. I do believe that I had an article saved that said that the oralists have actually partnered with the audiology industry to lobby for earlier implantation. As a general rule the age limit is 12 months, but we do know that imlants have been authorized at even younger ages. Logic would dictate that the FDA did not lobby themselves on this issue, and it was not a God-given inspiration that made them authorize earlier implantation. So, I assume that what I heard was true; the CI industry and the oralists lobby the FDA.

I feel hurt that you would think that I would rob a child of their right to hear. I understand that you are adamant about implanting your own child and that you think you made a good decision for him/her. I pray to God that you experience nothing but the best from your decision and that your child grows to have a full life and reach his potential.

I understand that the oralists and some other researchers believe that early aquisition of sound will encourage language development better; thus, we must implant babies as soon as the screening shows a hearing loss of any sort. Is there an age limit that you feel is appropriate? Should they automatically implant children who are HOH, or only deaf in one ear? How much hearing loss must a child display before he is automatically wheeled off to surgery so he won't be a drag on society? I am truly curious to see where you think the line should be drawn.

Do you have any statistics from a LONG-term data collection that shows the absolute effects of sending electrical impulses into someones head? A whole lifetime of say, 60 to 100 years of electrical impulses invading the brain has not been documented to my knowledge, but if you have the data, please share.

I am curious. If an implant does not benefit a person or is causing a problem, does state insurance pay for a new surgery to have it removed? Is that saving the tax payers money? I am confused.

Have you heard of human error during and afer surgery in hospitals? Is it not possible that a tiny baby with the smallest of ear canals and nerve system might be accidentally injured during a surgery? Is that terribly hard to concieve of. I realize that the claim is that implants are SAFE. But ya know, they said the same thing about electric shock therapy to cure depression, and the same is true of breast implants and lypo suction. Ya know, they use to promolgate LABOTOMIES too, until someone decided that it was unethical to experiment on people by giving them an irreversible and life-changing operation,, just so they would not be a drain on society.

Can you guarantee me that if we were to seek an operation to remove my granddaughters nodule, with only a slight hope for success, can persoanally guarantee me that she will not contract an untreatable staph infection or flesh eating from the surgery? These germs are mutating faster than we can create medicines to combat them. I know this is true because I just lost my husband from a staph in fection that he contracted in the hospital during a minor back operation. It ate through his spinal cord, and he had a massive stroke that made him brain dead, and on our anniversary, they pulled the plug. Any major invasive surgery can cause death due to the above mentioned complications, a blood clot or any number of reasons.

I want people to hear. But if they can't, I love them just the way they are. They don't need to undergo a painful and unpredictable surgery to accomodate me. I hope this doesn't sound crass, but it is on topic: If your child would have died from a secondary complication, what would you feel...especially if he were not old enough to express his desire or lack of desire to have the surgery inspite of the potential risk to his health?

Did you even read the FDA website??

After you do, please return and lets have a civilized discussion about this. Like I said, at least I care enough to try to be sure that people have access to all of the information available before making such a huge commitment. I was not trying to offend you for your choice, nor am I trying to do that now. I just want to be sure that comprehensive alternatives to the surgery are presented, and the risks are rightly represented. If we are looking for a happy story, the implant industry has already provided lots of glowing accounts for us to access. Unfortunately, I have not yet been able to find their accounts of the not-so-gowing experiences.

You are apparently an intelligent and educated man. You made a decision based on what you believed to be true after you were presented the facts. I am not sure that all hearing parents have done there research as thoroughly as you and I want to encourage to do so. Again, I apologize if my typing does not reprsent my whole thought.


That risk of infection or human error is just not worth it for me. If I had a deaf baby, I wouldnt subject him/her to those risks for the sake of hearing. I know that he/she will get language via ASL and dont need an implant to develop oral skills as myself was able do that successfully without implants. If I went ahead with the surgery and my baby died or had complications, the guilt would consume me. I know that the risks are small but they are there.
 
I am referring to your comments about saving the taxpayers money by not sending your daughter to the Deaf schools. When I read that I recalled a woman of a deaf daughter with CIs blog about how her goal is to get all the Deaf schools shut down cuz it would save taxpayers' money.

To me, that kind of view shows that money comes first. If all the deaf schools were shut down, where would those deaf kids who fell so far behind academically in the public schools go? Guess it doesnt matter cuz that woman's and your daughters are fine being mainstreamed. Doesnt matter if those other children return to the very same schools that failed to meet their needs and they end up worse off.

That is what I mean..in addition to the goal of cochlear implants saving money for the general taxpayers. Just like with cutting all kinds of programs that serve people with mental illness, addiction, youth advocating, and so much more.

I totally agree with Shel! I have read,, no first hand knowledge,, that many children who are implantees can't master oral skills. For whatever reason, no matter how many grueling hours they spend in speech classes, at the risk of their other academics failing, such as literacy, they still can't learn to talk in a way that doesn't come out so measured that they sound ,forgive the term, retarded.

As a result of this, they feel totally depressed and lose self esteem because they feel hopeless to ever fit in with their family or society. They hate to disappoint their parents, and they also hate being left out of every conversaton that they can't understand let alone respond to verbally.

There have been Deaf schools who report that they have enrolled imlanted children who are transfering from a mainstream school, most of these children are way behind in all of their academic studies especially literacy.

So, for the ones who only get a small amount of sound, and their is no burning -bush -miracle such as your daughter experienced, where would you suggest that they gain access to an education and social life? How many years should they be forced to repeat grades in public school before you are willing to allow them access to their own language and their own peers?

Rick, forgive me asking this, but I gots to know: Are you so ashamed of deafness in general, and your own daughter's deafness that you would disallow her the benefits of a loving Deaf environment where she recieved a means to communicate and socialize, and to learn? What if her implant had not worked? Who would you have turned to then? What if she was not cognitavely able to learn English skills? What then? Would it still be a waste of the taxpayers money to offer her an education in a Deaf school?

Your daughter happens to be very lucky, and maybe even an exception to the rule. Because she has the capabilities, and her implant was successful, it by NO means indicates that other children share her capabilities, implanted or not. I personally think that you should be thankful for all that she has been given, nurture her and provide all that you can for her... But please don't forget.... If the implant fails, or some other injury or illness were to force it's removal,,, and at night when she sleeps, or in the morning when she showers, or when she is near airport screening equipment etc,,, Any time that her implant is turned off... She is still DEAF. And we would love her and welcome her implanted or not... Can you say the same?
 
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