society's_child
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- Sep 27, 2006
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I simply choose not to have it for myself if my hearing has degraded to the point where HA is useless.
Has your hearing deteriorated that badly?
I simply choose not to have it for myself if my hearing has degraded to the point where HA is useless.
again - direct your complaint to FDA at 888-463-6332 to clarify its statement regarding risk
and I'm not opposed to CI at all. I simply choose not to have it for myself if my hearing has degraded to the point where HA is useless.
you are free to do so. I merely chimed in for other ADer. beside - you and Faire have already provided the benefits of it. it's important to show the risk, right?If you're not opposed to CIs, why not mention the benefits instead of the risks?
that's cool.As far as the FDA is concerned, I don't need to call them. I'm a bilateral CI recipient and have done plenty of research in regards to risks, etc. and am quite happy with the choice I've made to be implanted.
Has your hearing deteriorated that badly?
oh no not yet. but yes it has been slowly declining. Must be my age! I'm just saying if it does, I'm not going to opt for CI. I'm perfectly happy with the way I am - with residual hearing or none
Ummmm, HELLO! The device and surgery is NOT cheap. The more people opt for it, the more insurance rates will rise due to the fact that health care costs are SKY HIGH!
Ummmm, HELLO! The device and surgery are covered by insurance. The more people who opt for it, the less insurance rates will rise due to the fact that less money is spent on audiological and ENT services not to mention hearing aid programming. A CI may cost $50-60,000 initially, but after that, the expense is lessened since a person only requires a mapping every 6 or 12 months. Compare that to a hearing aid user who requires several visits for tweaking, annual hearing tests and a consultation with an ENT when problems arise with their ears.
Healthcare rates are sky right right now due to the expenses doctors charge for their services overall. Don't pin it on CIs because CIs have nothing to do with it.
If you're going to cite a source, then you need to back up your statement instead of making a generality about risk. You didn't indicate what degree of risk. You simply stated that there was a risk. I also said there was a risk of me crossing the street and getting hit by a car. So? Does that mean I shouldn't leave my home? Just because there's a small risk of facial paralysis, does that mean I shouldn't take the chance of being able to hear better? If you are opposed to CIs, that's fine, but don't exaggerate risks where little to none exist.
you are free to do so. I merely chimed in for other ADer. beside - you and Faire have already provided the benefits of it. it's important to show the risk, right?
that's cool.
She seem one of the few CI user here who are not trying to push it for everyone.
I never heard of a safe surgery.. There's always a risk.
I'm not pushing the CI. In an earlier post I said that I encouraged people to use whatever communication technique or techniques worked best for them.
But either way, you still have to go for adjustment rather it is for CI or hearing aids if your hearing is changing.
I know. I am saying it badly.
I mean she does tell the risks and non sucess stories too.
I know you are very sincere.
Typically CI hearing does not change over time.
Having said that, most CI users have annual or bi-annual mappings which is still less than the amount of programming, hearing tests, etc. that hearing aid users have. When I used to wear hearing aids, my hearing aid audis required me to have hearing tests every 3 months.
Every three months? wow.
I know. I am saying it badly.
I mean she does tell the risks and non sucess stories too.
I know you are very sincere.
DD,
I don't understand why you think doctors are promoting CIs to everyone who walks in the door because that simply isn't true.
I went to an Audiologist recently hoping to obtain a tactaid7. I was even willing to fund it myself. I just needed an Audiologist to purchase it since they don't sell directly to the public.
Anyway they recomended a CI instead. Since a Tactaid7 is much cheaper, I can't understand why. I don't want a CI because I like being profoundly deaf. The tactaid would just alert me to environmental noise through tactile means.
I also do talks at my CI centre to potential candiates. My centre puts people of similar deafness (profound deaf since birth, good speech and CI in adulthood) as me in my group.
I have a question... is there anyone on the site that did not benifit from CI. I know one Travis (smithr) he had his removed due to on going headaches but i can't recall anyone else?
Another thing is that when i say that i am CI user some deaf people do get quite negative about it and we haven't done anything wrong, we have nothing against deaf people who believes in strong deaf culture/keeping the deaf community alive... so am I...but they are the ones who pushes us out.