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A journey into the deaf world
Reflection about people who are deaf
A journey into the deaf world
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Perspectives of individuals with/without hearing impairments: Heather is the young girl who the documentary is surrounded around. She is deaf but wants the cochlear implant. She wants to belong in the hearing and deaf world. She wants to be able to communicate with non-deaf friends and talk on the phone, as well as support her family when it comes to communication. Heather’s father is deaf and without a hearing aid or cochlear implant. He does not have access to the hearing world as he only communicates through sign. He does not agree with the implant as he believes it is a scary and invasive surgery that creates robots. He believes that verbal speech is void of emotion whereas sign is natural and full of meaning and emotion. However, he admits …show more content…
They wanted to provide every opportunity in the world for their son. They had witnessed the first hand struggles that their immediate family members went through and did not want their son to go through the same things. Heather’s aunt’s parents are both deaf. They are afraid of the cochlear implant because they believe that the implant would eradicate the deaf community as a whole. 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 …show more content…
Kelsay and Tyler (1996) conducted a survey that asked parents to identify what they believed were the disadvantages and advantages. Several advantages identified include: awareness of environmental sounds, improved perception of speech, and improved production of speech. Some disadvantages listed were: equipment maintenance, slower rate of progression of auditory and speech skills, and the child resisting wearing the implant. After implantation, parents were asked to complete follow-up surveys to identify advantages and disadvantages of the implant. The study found, through progressive surveys done at 1-year post implant, 2-years post and 3-years post, that there was an increase in advantages and a decrease in reported concerns about disadvantages as time progressed (Kelsay & Tyler, 1996). Considering that this study was done in 1996, I think it is safe to say the the medical procedures have progressed and have been become more widely known and accessible and therefore, have had growing positive reports post-implant. I think it is important to critically reflect on this study. Obviously, to every parent who wishes that their child would receive a cochlear implant, there are parents that do not want their children to receive this surgery. This study only surveyed parents who
She longs to understand her hearing friends and have the ability to hear. Chris’s family, however, has opted to give their deaf son, Peter, a cochlear implant against the wishes of Mari’s Deaf parents and the Deaf community around them who feels it as wrong. Peter and Mari wish to give their deaf son the same opportunities as their hearing child because they are twins. Peter’s family investigates more about the cochlear implant by visiting families who have opted to give their children cochlear implants, but also go and visit the Maryland School for the Deaf to explore all sides of the argument. All the while, Heather’s father is against the idea, Heather’s mother is supportive at first but then changes her mind. Heather’s grandparents fight for Heather’s choice to receive the implant, but ultimately, the family decided that it wasn’t the right
Overall, I enjoyed reading the book because it opened my eyes to the deaf community and all that they go through which hearing people take advantage of. The autobiography doesn’t just tell you what his life was like; he makes you feel his emotions through every journey by explaining with countless details. The author wanted to stress how he had failed as a hearing person, and he just wanted to be appreciated as himself. As his eyes open to the deaf world, mine did too.
In the following chapters, there is an extensive amount of knowledge to learn about how Deaf culture is involved in our modern world. The pages assigned give us an outlook of how Deaf people are treated in our daily life, and how we should learn from it. Its gives a clear line between what are myths and what are facts, to those who are curious about the Deaf community or have specific questions. This book has definitely taught me new things that I could put to good use in the near future. In specific chapters, my mind really opened up to new ideas and made me think hard about questions, like “why don’t some Deaf people trust hearing people,” or “do we need another ‘Deaf president now’ revolution?” I realized many new things in the course of reading this book, and have recommended this to my family.
What I found most interesting about Jarashow’s presentation were the two opposing views: Deaf culture versus medical professionals. Within the Deaf culture, they want to preserve their language and identity. The Deaf community wants to flourish and grow and do not view being deaf as a disability or being wrong. Jarashow stated that the medical field labels Deaf people as having a handicap or being disabled because they cannot hear. Those who are Deaf feel as though medical professionals are trying to eliminate them and relate it to eugenics. It is perceived that those in that field are trying to fix those who are Deaf and eliminate them by making them conform to a hearing world. Those within the Deaf community seem to be unhappy with devices such
It was painful to see how hard the parents worked to get Lynn to be normal like the rest of the family. They spent so much of their time focusing on getting her to talk and read lips that they overlooked one huge factor: that no matter how hard they tried, Lynn was deaf. It was so frustrating to see how much resistance they had towards using sign language. It was sad to see how disappointed the parents were when they learned of Lynn’s deafness even though it was easy to see they loved their child very much. I feel as though this book was a great look into how the world wants to fix, and repair people with disabilities and how strong and proud the deaf community is that they would rather consider themselves to be special and of their own culture than to be considered less abled than a hearing person. I like that the story started off with the parents frantically trying to fix Lynn, and ultimately led to their love, acceptance, and celebration of their daughter’s deafness. In the beginning of the book Thomas and Louise are told not to treat Lynn like she is deaf because then she will act
Marika Kovac-Houlihan’s TED Talk hurt me. Hearing her stories first hand truly reveals the discrimination Deaf people face. It’s an easy to listen and understand the definition of discrimination but to experience it or witness is different. Kovac-Houlihan’s intention was for the audience to be stunned by her experiences, I imagine most of those people feel the same way I currently do. Her understanding was that most hearing people see Deaf people as disable or inferior, not every hearing person thinks that way, but most do. Kovac-Houlihan believes hearing people’s assumption is “that a deaf person may be isolated, uneducated or without language” (2:29 Kovac-Houlihan). I slightly disagree with her, but there are exceptions to every rule, one individual does not always impact the thoughts of the mob. I choose this video because of my reaction to Kovac-Houlihan’s primary discussion topics: the phonocentric ideology, loss of identity, and the divide between hearing and Deaf
Many people never realize or take much notice on what deaf people go through in life, but by watching the movie "Love is Never Silent", hearing people are able to have a clear view of what it is like to be deaf in the hearing world. Many different perspectives towards how deaf people live, socialize, party or work are built by many distinctive types of people. As the movie "Love is Never Silent" shows, Margaret and her family are isolated from their community. They aren 't allowed to sign in front of the hearing because it 's strange and abnormal. Seeing a deaf person sign during a time where being different can make a person look like an outcast makes hearing people pity the deaf and end up treating them as ignorant people. Although deaf
Lane, Harlan (1992). “Cochlear Implants are Wrong for Young Deaf Children.” Viewpoints on Deafness. Ed. Mervin D. Garretson. National Association of the Deaf, Silver Spring, MD. 89-92.
Me being pregnant and taking ASL has made me think a lot about life. Think about what would it be like if I was deaf or my baby was deaf how it would be hard to communicate if I have not talking the ASL class and how others would view me. I still really don't understand why the FDA could put out the cochlear implant out for children and adult when they haven't done the long term effects. The way people view others who are not the same as the norm don't really now what the world is like out there and sometimes I think that people do that to make themselves feel better. Know that I have realized that the hard life that people in institutions went through makes me want to go to the NYSARC and listen to all the stories that I kind didn't really listen to in the first time. I also take time when I am at work and talk to the deaf people even if I don't understand everything that they say but it feels good to be helping them find things and just listening. My thought is that people don't want to know what is different from them and that for some people its all about the way you are
The documentary of “Through Deaf Eyes” has open my eyes to the deaf culture. The movie has made it “click” that deaf people are just that people and individuals like me. Deaf community has its struggles just like everyone else. They struggle with growing into who they are as a person, harmful situations, and feeling a sense of belonging. They just speak a different language like Italians and Hispanics. Communicating with a different language does not make them lesser than a hearing person. When able to learn to communicate, the deaf are able to learn and gain knowledge just like a hearing person. The only difference is they have to learn more and work harder to achieve their goals and gain knowledge, which a hearing person learns just by hearing their surroundings.
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...
In this paper, I will be discussing Sharon Duchesneau and Candy McCollough’s thoughts on creating a deaf child. I will first explain Sharon and Candy’s argument for creating a deaf child. I will conclude by explaining and responding to a possible objection that could be made to their argument.
Getting my first cochlear implant was a very big deal for me and one the biggest event that has happened during my 17 years of life. The process that lead me to being diagnosed bilaterally profound deaf and if I would be eligible to get a cochlear implant also tie with this significant event. I do not necessary remember how I got diagnosed as deaf but I do remember wearing hearing aids when I was around two or three but I was not catching everything my parents or other people were saying. For example, I have one vivid memory of me and my mom in my house on the staircase leading to the second floor and I remember mom talking to me but I did not know exactly what she was saying. However, as my hearing continued to decline the hearing aids were
With cochlear implants it will allow the hearing impaired to live an average life. People obtain cochlear implants have intensive testing and evaluation to see if they are the right type of candidate for the implant. Some candidates even have to go through psychologist assessment. Finding the perfect candidate for this type of surgery is particular. People that do benefit from hearing aid are not good candidates. Audiologist want patients to have completely no ability to hear. Patients that receive the implants are have to undergo speech therapy to understand language.