Socrates said:Red Rum and Liebling, please take your personal attacks at each other in PM. You both have a precious friendship, value it please!
Socrates said:Red Rum and Liebling, please take your personal attacks at each other in PM. You both have a precious friendship, value it please!
coffeeeeman said:I am hearing so I can not appreciate the deaf communities feeling towards the CI. I do however have an opinion.
It is in my opinion that being deaf is a handicap. Not a handicap where being deaf prevents you from functioning but non the less a handicap in that you function as a minority in a world that is primarily geared towards hearing people. A handicap in that it's kind of like eating ice cream..when all you have in the store is vanilla you are comfortable with vanilla you know of nothing but vanilla. When offered something with a flavor to it..something that tingles the senses allows you a different perspective it is shunned at first. People in general are resistant to change when they are comfortable. Why have chocolate ice cream when vanilla is perfectly fine?
People who are born with non functioning legs rely on wheelchairs, crutches etc to minimize the impact of being a person who is handicapped, as I define handicapped as a minority.
The CI to me represents the wheelchair or chocolate ice cream. It's an alternative.
It was designed and in use to minimize the barrier of being a minority not to take away from the deaf community, but to allow them to feel less isolated when dealing with the hearing world. It levels the playing field. Granted Chocolate ice cream doesn't level out any inequalities but it sure as hell tastes good from time to time.
Mike
Opinions are like assholes everyone has one.
Originally Posted by Socrates
Red Rum and Liebling, please take your personal attacks at each other in PM. You both have a precious friendship, value it please!
Red~Rum said::-o I, Red~Rum gave up DAYS ago. Don't you start!!
I understand both viewpoints. On one hand Early Intervention is key....on the other hand, it is VERY hard to accurately tell how well a baby hears. That's why even up to a few years ago, the average age of dx (even for profound and severe losses) was something like 2 1/2 years old. I know we have ABR tests, but I know I read somewhere that even with those, a lot of dhh kids were still falling through the cracks. I also hear that the ABR is kind of unreliable...I've heard of kids who test as profound on ABR who test as hoh for traditional soundbooth/play audiotremy. I've also heard of kids who are hearing but who don't pass ABR.The issue of implanting deaf children with CI's at such a young age, remains very controversial. I'm not really for CI's to be implanted in kids under 7, but I cannot decide for every parent who wants their child to be implanted at a young age. I do acknowledge the decision should be based on the child's desire to get one or not.
Loomis said:hey sweet kj tell that to my son who was born deaf implanted at one and now speaks just as well as hearing chilren his age. He never knew what sound was till he was implanted. WAY TO GO ANOTHER STUPID COMMENT!!!!
Yes, even today there are still a significent number of kids who go through oral programs/ auditory-verbal therapy who while not "classic" oral failures, (can't speak at all) still can't pick up enough spoken language to commuicate in speech alone. I'm highly skeptical of the claims of oralists. They now claim that almost all dhh kids can learn to speak and hear, but they were claiming that many years ago too! (in the '70's and in the '60's too!)It's just that the success rate isn't as high as in those who have experienced normal hearing. Your son was one of the lucky few. Congratulations.
kristy said:i beleive that the doctors are trying to pull deaf peoples are not involved with deaf culture...
kristy said:I need to defend the doctors. They did not tell me about getting a CI. I am very involved in deaf culture yet I have a CI.
There is a growing acceptance of deaf folks getting CI s on their own, whether they are a part of deaf culture or not.
I made this very own decision on my own.
Meg said:kristy said:i beleive that the doctors are trying to pull deaf peoples are not involved with deaf culture...Same here, I researched on CI for 2+ years and decided to get one, that was AFTER I was a anti-ci person. I have CI now.. Doctors does not play a role in pulling those deaf people who do not relate to deaf culture.kristy said:I need to defend the doctors. They did not tell me about getting a CI. I am very involved in deaf culture yet I have a CI.
There is a growing acceptance of deaf folks getting CI s on their own, whether they are a part of deaf culture or not.
I made this very own decision on my own.
Boult said:I researched on CI for 2+ years and decided to get one, that was AFTER I was a anti-ci person.
I also researched for 3 years. My older brother, his wife and their daughter all got CI s at the same time. I was furious and angry at them. I refused to talk to them for a long time. I felt betrayed by them.
Looking back, I know it was silly but I was very antiCI and was feeling threatened by it.
Over the years, I have mellowed out and did research..thus came to the conclusion that life is too short not to try anything - we all need tools to make our lives easier.
Of course I wont give up signing - its my language but CI will help me cope better in other situations.
Meg said:Agreed!Boult said:I researched on CI for 2+ years and decided to get one, that was AFTER I was a anti-ci person.
I also researched for 3 years. My older brother, his wife and their daughter all got CI s at the same time. I was furious and angry at them. I refused to talk to them for a long time. I felt betrayed by them.
Looking back, I know it was silly but I was very antiCI and was feeling threatened by it.
Over the years, I have mellowed out and did research..thus came to the conclusion that life is too short not to try anything - we all need tools to make our lives easier.
Of course I wont give up signing - its my language but CI will help me cope better in other situations.
but I do not try to prevent my friends from getting one, When they told me how they experienced and corrected me my spewing misinformation years ago, I realized and started researching it. Although, I liked to hear and wore hearing aid all the time. So, after getting it, It was best thing I ever done! almost everyday, I would snap fingers as if it is music to my ear. with my HA, I can't hear it in slightly noisy environment! But with CI, I can hear no matter where!
So far, I really enjoyed my CI. best decision I ever made!
Very healthy attitude to have! I think more Deafies will stop criticizing those Deaf who decide to get CI, when they realize that it doesn't make you a hearie but it's just a tool that might help deafies cope better with more hearing world situtions.but CI will help me cope better in other situations.
deafdyke said:Very healthy attitude to have! I think more Deafies will stop criticizing those Deaf who decide to get CI, when they realize that it doesn't make you a hearie but it's just a tool that might help deafies cope better with more hearing world situtions.
DeafSCUBA98 said:I have been thinking of getting an CI myself. and been researching for near 2 years. I have been told some friends about myself thinking of getting one.. some of them seems like disappoited that i choose to get one, however they didn't turn against me. some of them support my idea. but i will say 1 out of 7 people turn against me. however they told me " you're 24 years old and it's too late for you to get one" i was thinking nah.. 24 is never too old.. there's 50 years left of my life..
i knew when i get one.. probally next year.. i have no clue how long it takes to get one. they might change their mind.. since i'm not planning on leaving deaf culture.. i'm staying with deaf culture.. but be more involved with hearing culture because that's a normal lifestyle. working with hearing, son's hearing it'll be lovely to hear him say "i love you" and so on.