Cochlear implants are used for people who are completely Deaf, not being able to hear a single noise or hard of hearing individuals as well. Sound waves go into the ear, entering the ear canal, then hitting the eardrums in which vibrates. Vibration from the eardrum pass major parts in the ear, them being the bone called the Malleus, Incus, and Stapes. These three main parts in the ear amplify the pulse, and then are picked up by small hair-like calls in the cochlea. Moving as the vibration hits, evidence is then sent through the auditory nerve then to the brain, the brain processes the data and in which we describe as sound. A cochlear implant is a highly invasive procedure where the surgeon drills a small hole into the individual’s skull; opening the Malleus bone then a small hole is drilled into the cochlea where the electrodes are inserted. This procedure takes about 2-4 hours, and surgeons use general anesthesia. Having a magnet under the skin/skull for the receptor to hook to, and also have to shave out all little hairs around the cochlea, and spending $40,000 for this implant. Deaf children should not get the cochlear implant because it’s a dramatically change in ones life and affects the way they feel and see themselves.
Cochlear implants can affect many children from the age after birth to twelve. This implant does affect children emotionally. Infants to toddlers don’t even know what is going on, they are to young to understand that they are deaf. Parents not accepting the fact their child is deaf and does not want to be part of the hearing world. Many parents whose child are born or become deaf do not want any contact with the deaf community; they just want to “fix” their child. Sad part is that the child has no idea is...
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...f their child. Agreeing that the CI cannot cure deafness, not saying all hearing parents don’t get involve with the deaf community and learning sign language but for the parents who do the exact opposite is what upsets many deaf individuals.
Parents that have deaf children believe the implant is beneficial for themselves and their child. In 1990 CI was first approved for many children at the ages from 2-17. So parents too the chance and did what ever is possible to have their baby hear. Strongly convinced the implantation is key to living life to the fullest. Kids with CI would be allowed to play with hearing kids around them and grow up hearing everything around them. Having their kids attend “regular” hearing schools and not having anything to do with deaf schools, because they believe deaf school are not taught at the same standard as regular speaking school.
The movie that I watched is named Sound and Fury. The movie follows the Artinian family, which is distinguished by two brothers. One brother, Peter, is Deaf and has a Deaf wife and three Deaf children, one of which is Heather, the focus of the documentary. The other brother is Chris, who is hearing, along with his hearing wife, Mari, and their twin sons. One son is hearing and other one, named Peter, is deaf. The family is at odds over the debate of cochlear implants. A cochlear implant is a surgically-implanted device for profoundly deaf or severely hard-of-hearing individuals. It provides the individual with a sense of sound by stimulating the cochlear nerve. A situation arises when Heather wants to have a cochlear implant and her parents do not really understand why.
This issue is important because if you try to force the Deaf to hear, they might not grow because they will have no form of communication to use with other people. Even though the doctors might say to not use ASL, this will greatly hinder your child's well-being in the long run. I learned a lot about Deaf people, ASL, and/or Deaf Culture after reading this book. Deaf people are normal, just like anybody else, and they should not be treated any differently. Some people treat deafness as a disease that needs to be cured, but it's not.
The movie “Audism Unveiled” was a very interesting and powerful movie. I never realized that deaf individuals are discriminated against. This could be partly because I have never been immersed in or educated about the deaf culture until this year. One of the things that struck me the most while watching “Audism Unveiled” was the many heart wrenching stories about children being unable to communicate with their own non-signing hearing families.. The deaf child would have to ask their family members, why everyone was laughing or what’s going on. The family members would just tell them “I’ll tell you later” or “Nevermind. It’s not important”, resulting in the individual feeling isolated. Personally, I agree with people saying that if a parent has a deaf child they should learn how to sign; communication is what brings families together. As a result, the most intriguing thing to me was the stories of family members never learning American Sign Language; leaving their family member isolated.
While the benefits for the hearing are great, there are better benefits for those who are Deaf. Jarashow stated that it was essentially frowned upon if a Deaf child was using sign instead of trying to use what ability they had to hear. This seems counterproductive and if they emphasized more on teaching Deaf children ASL, there would be better outcomes for them in the future. Instead of focusing on trying to make everyone the same, they should focus on giving these children the best opportunity possible despite their
Cochlear implants are amazing feats of biomedical engineering, and have helped many people regain the ability to hear. While there are some ethical dilemmas that go along with them, there is no denying just how amazing these implants really are. By understanding how the ear works, what causes it to stop working, and using science and engineering to fix that problem, there is now a way to give someone a sense they might have never been able to experience. It can be costly, but it could drastically change someone’s life. Some people may say for worse, but there will always be someone else to say it was for better. Overall, cochlear implants are an incredible invention and will continue to grow and only get better with technology.
Is acquired deafness more traumatic psychologically than developmental? Does being deaf have positive characteristics? How does being deaf affect relationships with family and
One excerpt mentioned that the idea that Deaf people are left with the burden of fitting into a hearing world was a product of “laziness” on the part of the Hearing. Instead of making adjustments to accommodate the Deaf, Deaf people are doing all of the work to accommodate the Hearing. Notwithstanding the major alterations that include learning to speak and wearing hearing aids, hearing people merely have to learn sign language. I’ve witnessed this in my own home. When my brother stopped speaking, it wasn’t ever a concern for the rest of the family to adjust to him, we continued on as if nothing changed. It’s true, Deaf children practically have no say in how they would rather communicate, it is left up to the parent and in most cases, Hearing parents. I’m just glad that I have an opportunity do the work to learn ASL and make strides in breaking down barriers that have hindered communication between the Hearing and the
In chapter seven, the one thing that stood out to me the most was the fact that the children would have a cochlear implant but still didn't feel like part of the hear or deaf. I the one sentence in the book that this was in was “the child's developing a social identity, a partially successful
Deaf and hearing impaired individuals are know longer an out cast group. They now have there own deaf community. Deaf individuals do not consider themselves having an impairment, handicap, or any type of disability. They believe that through the use of sign language, other communication skills, and technology that there deafness is the way they are supposed to be. Many people who have perfect hearing can not understand deaf people and why they embrace there deafness instead of trying to receive hearing and get rid of there handicap. However not all deaf people have th...
In the United States today, approximately 4500 children are born deaf each year, and numerous other individuals suffer injuries or illnesses that can cause partial or total loss of hearing, making them the largest “disability” segment in the country. Although, those in the medical field focus solely on the medical aspects of hearing loss and deafness, members of the deaf community find this unwarranted focus limiting and restrictive; because of its failure to adequately delineate the sociological aspects and implications of the deaf and their culture. Present day members of deaf culture reject classifications such as “deaf mute” or “deaf and dumb”, as marginalizing them because of their allusions to a presumed disability. (Edwards, 2012, p. 26-30)
The deaf community does not see their hearing impairment as a disability but as a culture which includes a history of discrimination, racial prejudice, and segregation. According to an online transcript,“Through Deaf Eyes” (Weta and Florentine films/Hott productions Inc., 2007) there are thirty-five million Americans that are hard of hearing. Out of the thirty-five million an estimated 300,000 people are completely deaf. There are ninety percent of deaf people who have hearing parents (Halpern, C., 1996). Also, most deaf parents have hearing children. With this being the exemplification, deaf people communicate on a more intimate and significant level with hearing people all their lives. “Deaf people can be found in every ethnic group, every region, and every economic class” (Weta and Florentine films/Hott productions Inc., 2007). The deaf culture and hard of hearing have plenty of arguments and divisions with living in a hearing world without sound however, that absence will be a starting point of an identity within their culture as well as the hearing culture (Weta and Florentine films/Hott productions Inc., 2007).
From a deafness-as-defect mindset, many well-meaning hearing doctors, audiologists, and teachers work passionately to make deaf children speak; to make these children "un-deaf." They try hearing aids, lip-reading, speech coaches, and surgical implants. In the meantime, many deaf children grow out of the crucial language acquisition phase. They become disabled by people who are anxious to make them "normal." Their lack of language, not of hearing, becomes their most severe handicap. While I support any method that works to give a child a richer life, I think a system which focuses on abilities rather than deficiencies is far more valuable. Deaf people have taught me that a lack of hearing need not be disabling. In fact, it shouldn?t be considered a lack at all. As a h...
Hearing loss is a major global public health issue. Hearnet (2017) defines hearing loss as “a disability that occurs when one or more parts of the ear and/or the parts of the brain that make up the hearing pathway do not function normally” (para. 1). There are many different types of hearing loss, which can have multiple causes, giving each individual experiencing the issue a unique hearing loss case. These types include Auditory Processing Disorders, when the brain has problems processing sound information; Conductive Hearing Loss, a problem with the outer or middle ear which prevents sound making its way to the inner ear; and Sensorineural Hearing Loss, when the Cochlea or auditory nerve is damaged and cannot
I think it is obvious to see how the people who are hearing are for the cochlear implant whereas the deaf community is more against, or hesitant, in regards to the implant. I will never begin to understand what it would be like to be in a minority group, like the deaf community. I come from a place of privilege where I do not need to fear about my identity being attacked. I can not begin to understand the fear of losing one’s culture and identity. However, I do believe that disabilities and conditions, like deafness, do inhibit one’s ability to succeed in the world – not because the person is unable to succeed but because of how negative stigmas affects one’s ability
First of all, when I was a baby, my Mom noticed that I was not responding when she called my name. Each time Mom took me to the doctor, the doctor said everything was fine. One time the doctor clapped behind my head to test my hearing. I turned to the doctor and the doctor told Mom, “See, he can hear.” When I was 18 months old, Mom asked the doctor, “shouldn’t he be talking by now?” The doctor said,” Boys are slow. My son never talked until he was 2 ½ years old and then he just started talking in sentences.” But, Mom didn’t give up. She took me to an audiologist to have my hearing tested. The audiologist diagnosed me as being deaf. This is where I was truly my own body, being deaf without a cochlear implant. My parents showed they loved and cared about me by not giving up when they thought something was wrong. This is kind of ironic because I was my own body and my parents wanted to change it for the good. Meaning that they want to give me a cochlear implant so I can hear.