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Just found the doctor's email on internet and let's hope it doesn't bounce.
I'm kinda embrassed to say this but I want to let my doctor know what implant I want and my parents are like let the experts decide. They aren't being of much help on this.
Well what do the experts know of what sort of situations I have to deal with on a daily basis? I have no idea how to contact my doctor or my audie. I tried to email a member of my doctor staff but my mail bounced.
I want to let them know that I want the Nucleus Freedom and that the HiRes is my second choice.
I really hadn't expected to hear from Dr. Pillsbury so soon and I'm really glad I got the answer from him. I'm impressed with the UNC people.
Well I'm glad you and I agree Hear Again!
Do you also think that people should experiment with different technologies before opting for bilaterals? I just think that bilaterals should be reserved for the absolute worst cases, and that most implantees should experiment. !
Well I'm glad you and I agree Hear Again!
Do you also think that people should experiment with different technologies before opting for bilaterals? I just think that bilaterals should be reserved for the absolute worst cases, and that most implantees should experiment. There are some people who are "right off the bat" canidates.....like I believe that people with auditory nereopathy should automaticly get bilaterals, no questions asked. I just think that b/c results are so indivdual, that bilateral implantee canidates should experiment with other technology in their better ear, unless of course testing indicates absolutly NO benifit whatsoever from traditional( hearing aids) and alternative (eg body worn aid, those high frequncy transponders) I mean I know a girl who had NO benifit (not even enviormental!) from '80's (including body worns!) and 90's types of hearing aids. She recently tried hearing aids again, and she's been getting SPEECH perception from her aids!
R2, I know that in countries with universal health care, they tend to be VERY conservative about implantation. Unfortunatly, the US tends to be totally market driven as to implantation. A lot, if not most implantations are legitimately needed. But having a market driven health care system can lead to a segment of the market being totally convinced that they GOTTA have the latest high tech gadget, whether it be the latest digital hearing aid or the latest CI, that can do everything but bake cookies. But don't you agree with me, that it's worth it to experiment?
I've never had any success using digital HAs. They never seemed to provide enough amplification and always seemed to distort speech more than my analog aids.
I'm sure that sometimes it happens - like the case that Hear Again mentioned of the person with the ITE hearing aids but a snapshot of this forum here shows that this is the exception rather than the norm. And yes I do agree that experimentation with other technologies before a CI should be done as a matter of course,QUOTE]
Yes -- CI criteria vary from CI center to CI center. Where one person with moderately-severe hearing loss in one ear and profound loss in the other may be implanted, another person with severe-profound hearing loss may not.
When insurance companies decide whether or not to pay for a CI, all kinds of supportive documentation is included such as a person's audiogram (aided and unaided), speech discrimination scores (HINT test -- sentence test in noise; sentence test in quiet; single word test) as well as observations about the way a person is/has been communicating.
The CI application my CI center required me to complete contained a multitude of questions including whether or not I could hear on the phone with both ears, left ear, right ear or neither, if I experienced difficulty communicating with others in a one-on-one situation and/or in noise, how my hearing loss impacted my ability to communicate, what kinds of daily activities were negatively affected by my hearing loss, what kinds of strategies (written communication, sign, FM system, etc.) I was using to communicate with others, how I felt about my hearing loss emotionally, why and how I thought a CI could benefit me, etc. If I remember correctly, the application was 6 pages long. So, at least as far as my CI center is concerned, people are evaluated thoroughly before they are considered a CI candidate.
Some CI centers (such as the example I gave of the person who wore ITEs before being implanted) may be more lenient than others, but generally I think all CI centers do everything possible to help anyone who walks through their doors to hear the best they can whether this means recommending the use of stronger HAs or a CI.
To my surprise, my CI audi told me that she has seen people with moderate losses (moderate across all frequencies) submit an application to be evaluated for a CI. In those cases, stronger HAs are recommended and people are advised to return for a CI evaluation in 6 months if they experience further hearing loss.
To my surprise, my CI audi told me that she has seen people with moderate losses (moderate across all frequencies) submit an application to be evaluated for a CI. In those cases, stronger HAs are recommended and people are advised to return for a CI evaluation in 6 months if they experience further hearing loss.
That doesn't really surprise me. There are some people are who don't really understand what a CI is about and think it's the latest hearing aid on the market that they have to have to paraphrase DD. As soon as you tell them that their residual hearing gets destroyed in the process though they have second thoughts.
That is what the screening process is for - to ensure that only those who need CIs get them.
That doesn't really surprise me. There are some people are who don't really understand what a CI is about and think it's the latest hearing aid on the market that they have to have to paraphrase DD. As soon as you tell them that their residual hearing gets destroyed in the process though they have second thoughts.
That is what the screening process is for - to ensure that only those who need CIs get them.
R2D2,
Good point. Even people with very, very little residual hearing are frightened of losing what they have.
One of these days I'm going to check out the Hearing Exchange website so I can see what DD is talking about.
I must say I don't like the idea of my CI being visible to all but hey I think the benefits outweighs a little vanity!
deafskeptic,
You'd be surprised at how many people *don't* notice your CI. I have long hair and like to wear my hair in a pony tail or braid. While I get comments and questions about my CIs, it doesn't happen nearly as often as I thought it would. Most people think my CIs are the "latest and greatest" Bluetooth headset. LOL!
As for Hearing Exchange, I'm going to check out the website later this evening. Perhaps there will be more people in the chat room at that time.
There are usually people in the chatroom in the evenings, like say around 7ish pm or so.
Oh agreed.....but I think that part of the reason why health insurance initially covered CI is b/c initially a relatively small number of people were eligable to be implanted. It was expensive yeah........but it was cost effective since in those days, only a small number of people were eligable to be implanted.I question as to whether health insurance companies wherever they are located would simply nod at unnescessary CI operations. I'm sure that it happens in a small number of cases but private health insurers have their shareholders to report to and as such they want to maximise profit by spending less