windy135
Posts: 437
Joined: 10/17/2005 Status: offline
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Hey everyone I did some reading and I found a persons opinion that pretty much matched my concerns so I'm going to copy and paste it. I'll also leave the address. Just so everyone know's I'm not saying this is the right opinion I thought it would be interesting to post and let us get a different view. Notes to take: this is over ten years old and I know many things have changed including the implant. But do you think that what she say's about how parents are approached has changed? (Contributed by Katherine C. Morehouse (Casey) [email protected] at 5 Jan 1994.) "Let me say here briefly that one of the reasons I have such strong opinions against cochlear implants in children, especially prelingually deaf, signing children, is that as an educational audiologist at a school for the deaf, I see and hear from parents constantly about the misinformation that they are given about cochlear implants,the misconceptions that they derive from the information they get, the lack of information that they are given about the deaf community, the tremendous pressure that is put on parents to get cochlear implants for their kids, the tremendous pressure they, in turn, put on their perfectly fine, well adjusted Deaf kids to get implants, the power struggles that are set up by this, between deaf kids and their parents, the kids not wanting to disappoint the parent, and the parent always expecting that "miricle". The anger the kid feels that "My mom not accept me deaf". And dispite what any one will say they tell parents about the pros and cons of cochlear implants, I have yet to meet a parent who was given(by the cochlear implant team) a list of the "failures" to call for opinions. The Deaf adolescents who actively decide to stop using an implant put in when they were 10, --they are never asked to talk to parents, the mother of the kid, whose implant failed due to ossification of the cochlea around the electrodes,---- she has never been asked to speak to perspective parents, the child with the drooping cheek, due to a a damaged facial nerve during the implant surgery, ----she was not on TV or in the newpaper.. I really could go on and on.. but....It seems these parents are given the list of "successes" ( a short list which is used over and over again.,as there are not actually a huge number of kids with these implants...so far) I have yet to meet a parent who was actively introduced to deaf adults, by a cochlear implant team, so that they could hear the other side, Actually, I have yet to meet a member of a cochlear implant team who know more than rudimentary sign language or who has any kind of active relationship with the Deaf community.. That is not to say thaty they are not out there! " http://www.zak.co.il/deaf-info/old/ci-opinions.html#unfavorable
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