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My experience when I was deaf
Reflection on deaf culture
My experience when I was deaf
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The documentary “For a Deaf Son,” delineates a young boy, Thomas Tranchin, who was born deaf into a hearing family, and the battle his parents endured to decide to teach Thomas in sign language communication, strictly communicate in English, or both. The documentary is educational for the hearing world to shape their own particular opinions on what type of technique would be better for their child in the event that they were to ever be in a comparative circumstance. As Dr. Carlos Erting expressed in the film, 93% of hearing impaired children have hearing parents; therefore, this documentary gives a glimpse at both perspectives of nonverbal communication and oral communication. However, as I viewed the short film, the clashing feelings of Thomas’ …show more content…
mother left a solid effect on me. Thomas’ mother strived for techniques similar to those used in Oralism; while, his dad became open-minded to Bilingualism for Thomas. As a mother, I would have considered a similar method as the father in showing my child ASL and English joined until he could determine the choice for himself. There appeared to be four occurrences throughout this film which captured my attention. The initial event happened when Thomas' older sibling, Matthew, articulated his emotions on Thomas' deafness.
In an overwhelmed hearing world, it was comprehended that Thomas would need to strive to convey what he wanted to express himself; however, I was not anticipating that Matthew would have the same amount of challenging time. When he illustrated that he would get harassed by different children for having a profoundly deaf sibling appeared to bring on an uneasy feeling to me. I feel that Matthew required as much love and acknowledgment as Thomas during this time, which he might not have received it to its fullest degree. He clarified that he was sad and cried for three days after the of discovery that Thomas was deaf. This was greatly heartbreaking to hear because although Thomas was not sad to be who he was, his family seemed to mourn what he was not going to be able to hear. In my opinion, at first the family made Thomas' inability appear to be difficult to work around instead of embracing it and showing Matthew all the positive things that could rise up out of having a deaf sibling. The second occurrence was during Thomas’ speech therapy sessions and at home with …show more content…
his mother. Thomas seemed to be frustrated with therapy and at some point conveyed to his father that he would not like to do the session. It appeared to have a great deal of stress for the family to do these hour-long sessions day by day with little to none advancement in his speech. Thomas’ inability to communicate his thoughts, feelings, or his personality to his parents affected me since I also have a four-year-old son. At four-years-old, he already has an enormous amount of personality and I know things such as what’s his favorite color, what toy he adores, dislikes and likes. In my opinion, I feel that if sooner or later I was not able to know these things than I would utilize nonverbal communication and signing because having that connection to my child would exceed a troublesome technique I believed was best for him. I however, cannot judge Thomas’ parents in their decision to try all they could with strictly oral communication because I have never been in their situation and I know as a parent it is difficult to see your child go through any obstacles in life. The third occasion was during the meeting amongst Myrna and Luis Orihuela.
In my view, I feel that I would have taken a similar form of instructing method that parents of Kenny Orihuela did. His mother desired to give Kenny choices so that he would be able to decide for himself in the future which led towards bilingualism. If he decided to sign later on she would approve of his choice and that seemed to draw my attention and convey my thought and feelings if I were in the same situation. During the interview, Kenny's father explained how rewarding he felt knowing that Kenny was able to hear a little more than before and that joy was directly shown through the interview. I my opinion, I feel that they are attempting to make the right decision to benefit Kenny, and they acknowledge that he is deaf and need to accommodate his needs instead of attempting to change him to suit their own needs. I firmly opposed the therapist’s thoughts that without practical speech, deafness determined what a person could do in their life. The reason behind why I differ from her opinion is because there have been many hard of hearing individuals who have not utilized functional speech and have still turned out to be exceptionally successful, for example, Leah Katz-Hernandez and Marlee Matlin. Lastly, the final event that caught my attention was the point at which the man was narrating to the children. What I think truly got to me was the interview with Nancy Shook, she stated Thomas is learning
words yet he is not learning concepts and ideas through signing. To watch the children, comprehend and remain intrigued by visual communication was an astonishing thing to view. The actor expressed he would love to see more parents acting thoughts out with their children, it reminded me of a few books I received for my son little while back. These books had no words just illustrations and the story dependent upon us to create. In my opinion, I believe doing these stories with Thomas would have given him a significant advantage as much as it would a hearing child. Imagination is an important key to child development and I think he would have had some sort of approach to express his thoughts and feelings through visual storytelling to his parents, perhaps this would have lessened the great a barrier between them. In conclusion, the documentary, "For a Deaf Son," was hard to watch because arose clashing purposes of perspectives for me; however, it was extremely educational for me not knowing anything about signing, oral communication and bilingualism. If by chance that I had a hard of hearing child, I would show him as much English as could be expected, thoroughly working with him, yet in the event that I can't comprehend what makes him frustrated and sad or things that he appreciates doing then I know I must learn ASL regardless of how tough it might be for me, I know it is similarly as tough for him to learn English.
Mark Drolsbaugh’s Deaf Again is a biography about his life between two dimensions of the Deaf world and the Hearing world as well as the implications he faced throughout his journeys’. Mark Drolsbaugh was born from two deaf parents and was basically forced to adapt to the hearing world even though his parents are deaf. When Drolsbaugh was born he was hearing, however, by first grade his parents and teachers discovered he was losing his hearing. As time went on Mark realized the issues he faced from trying to adapt to the hearing world. Mark Drolsbaugh quotes in his biography, “Deafness is bad. I am deaf. I need to be fixed. I must be like them, no matter what, because deaf is bad.” However, no matter what his family believed that he
Have you ever felt like there was nothing that you can do for your child? In this book, Deaf Like Me, by Thomas S. Spradley and James P. Spradley, I can see the journey that Lynn’s parents took to get her help. (Spradley & Spradley, 1978). This book was an excellent read. I really liked the way that they described the ways they tried to help Lynn to understand the world around her. The book, is a great asset for any family that might be unexpectedly put into a situation that they know nothing about such as a deaf child.
At this time in history, those who were deaf were tried at best to be converted into hearing people. Doctors, speech therapists, and audiologists all recommended the use of speaking and lip reading instead of sign language. Since Mark’s grandparents were hearing, they were closer to the parental position instead of his deaf parents. His grandparents provided him with the best possible education he could get, startin...
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. If a parent comes to learn that their child is deaf they react very crazily and act like their child is dying and that deafness is some fatal disease. Deaf people should be treated just like anyone else and no differently. They are not disabled and can do great things in this world.
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.
Kimmy Bachmann A Journey into the Deaf-World Chapter 1 The narrator begins this chapter by introducing himself as well as his colleagues and co-authors. Ben Bahan, the narrator, is a deaf man from New Jersey whom was raised by deaf parents and a hearing sister. After spending an immense amount of time studying American Sign Language (ASL) he moved on to now become an assistant professor at Gallaudet University in the Deaf studies Department. His colleague Harlan Lane, a hearing man, is a specialist in the psychology of language and having many titles is a key aspect of this book as he believes, as does most of the Deaf-World, that they are a minority language and takes up their point of view to the hearing world.
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
His parents have different opinions on what’s best for him. His father thinks that he should learn to lipread to be as normal as possible as well as wearing a hearing aid. His mother wants him in a ASL cassroom where he can learn at his pace and understand more things then he is in the classroom he’s currently in. As maybe with other hard of hearing characters in film, the mother can sign but the father cannot as a result of this he is totally out of touch with his child and his needs.
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 this article, “The Deaf Body in Public Space,” Rachel Kolb explains how interacting with people who do not understand sign language could be difficult. With her hearing disability she struggled to communicate with her peers. Kolb further explains the different situations she has encountered with people and comments that are made with first intercommunications. Going further she also mentions how she struggles with two languages and two modes of communication.
Watching this film has made me realize that Deaf Culture has come a very long way. In 1800’s, Deaf people were very misunderstood and were often seen as strange or mentally retarded (ASL IVC). People thought this way because it was something different than what they were
With that knowledge the deaf character gained more confidence when communicating and was able to achieve bigger goals in their life then when they had little to no knowledge of how things worked in society. Reading about these characters just gave me a small insight into the deaf community but with the documentary ”Through Deaf Eyes,” has open my mind and eyes that they are people who can thrive in and change the world just as anyone can when they put their mind to
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...
Imagine seeing people speaking, moving their mouths and not being able to hear anything. Welcome to the world of deafness. The journey for someone who is deaf can be challenging, but those challenges can be overcome with perseverance. Today I am going to share with you the story of my journey with deafness and see that if I am my disability. It is an experience that has shaped my life through body, mind, and spiritual matter.