I'm so excited to be taking accelerated English in your class this year! I've heard so many good things about you and your class. I'm not going to lie though, I'm more of a math and science person than an English person. I feel that this year with a fun class, I'll be able to accelerate in English.
Each school year is always a very big adjustment for me. I have a hearing loss in both ears that requires me to have hearing aids. Ever since I can remember I've had to communicate with my teachers to figure out the best way for them to help me.
As soon as I was born the doctors checked my hearing to see if there were any abnormalities. They knew right away that something was wrong. Both my mom and my grandma are almost deaf in both ears, so they
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They put me in a box and connected me to a bunch of wires. I felt like an alien that was getting tested on, but I soon came to find out it wasn't as awesome as I thought. When I finished the series of testing I stepped out of the box and we were given the news. I needed hearing aids.
As I'm sure you know, hearing aids aren't cheap. My family couldn't afford to get me the hearing aids I needed. We made some calls, and I ended up doing a commercial. In exchange for the commercial they paid for my hearing aids.
When I was little having hearing aids was the coolest thing ever. Everyone wanted to see and touch them. We thought that I had robots in my ears. As the years have gone by from elementary school to my first day at Borah that has changed a lot.
I am so scared to let people know I'm different. I get horrible anxiety when we have discussions as a class because I can never hear what anyone says. People always laugh at me now because I always have to ask them to repeat themselves. My immediate default setting is to use this as my weakness. I rely on my mom or my dad to communicate to people when I'm too scared
Like I said before I was unaware deaf experienced audism. By educating others they will be more aware of this ongoing issue resulting in preventing audism from occurring. Another way to reduce audism is to spread the word to friends and family. Explain to them about this issue and have them spread the word as well. Lastly, if you see someone being an audist, kindly ask them to stop as well as explain to them about the damage they may inflicted on someone. This will be a learning experience for you as well as the other person
Marie Jean Philip was born on April 20, 1953, in Worchester, Massachusetts. She was the first-born child. Although she was born to deaf parents, Marie’s deafness came as a surprise for her parents. She had two sisters whom were also deaf. Deafness was hereditary in her family, however not everyone in her family was deaf. Marie’s father had one sister who was deaf and her mother had two siblings who were also deaf. When Marie was 11 months her parents noticed that she wasn’t responding to all noises. Her parents decided to test her hearing one day by creating noises behind Marie to see if she would respond. When Marie responded only to the loudest of noises, such as pots banging together, they found that at times she could hear with her right ear, but she could not hear anything out of her left.
In support of Gallaudet University's, “Deaf President Now!” protest, Rev. Jesse L. Jackson once said “The problem is not that the deaf do not hear. The problem is that the hearing world does not listen.” (Lee) This concept been seen throughout Deaf history; Today it is especially noticeable now that technology has been developed to restore some hearing to many who are deaf. However these seemingly miraculous devices such as hearing aids and cochlear implants (CI) are a gilding for the real problem. CI’s in particular are thought to be a miracle cure for deafness, this misconception causes a great friction between Deaf and hearing culture. Deaf people should not be expected to get CI’s to “cure” their deafness for three primary reasons: CI’s promise more than they can deliver, they are an affront to Deaf culture, and ASL is a more effective way to insure development.
If you had a fear only you could understand would you tell people? Would you think other people would find it silly? Fear is something everyone has, Mary Seymour writes about her fears of sharing personal information in her story “Call Me Crazy But I Have To Be Myself.”I also have fears that have stopped me from being myself. It takes a long road to recovery from fears to get where you want to be.
A hearing loss can present many obstacles in one's life. I have faced many issues throughout my life, many of which affected me deeply. When I first realized that I was hearing-impaired, I didn't know what it meant. As I grew older, I came to understand why I was different from everyone. It was hard to like myself or feel good about myself because I was often teased. However, I started to change my attitude and see that wearing hearing aids was no different than people wearing glasses to see.
At a young age, I witnessed my younger brother lodge an eraser in his ear and later have it removed by a doctor. A year later he had tubes inserted and a year or so after that, I saw those tubes fall out of his head. Besides thinking that my younger brother was really a robot with metal parts falling out of his brain, it was where my fascination of the human ear began. Since then I’ve helped my grandfather and father with their hearing aids, especially replacing the small batteries which was difficult for their large farmers’ hands. I’ve also observed my older sister, an Audiologist in California, for two weeks as she worked with patients, letting me do hearing aid cleanings, help with sales, file patient records, observe ear molds being
According to Chapman et al., (2000), the loss of hearing appears to be a chronic issue through...
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
The current hypothesis is that one of my genes is a mutated gene, that mutated gene is what is causing my hearing loss. If this is the real reason why I have hearing loss, there is also worry for what other problems does this mutated gene cause. With finding a mutated gene, they will most likely be able to predict how much worse my hearing will get. Another possible but not likely cause is a tumor, currently, I have to get an MRI to make sure that there is no growth inside of my head. If there is a growth, that will lead to some serious issues. The last possible cause is that loud noises have damaged my hearing, but it is even more less likely than a tumor. I am almost never exposed to loud music, concerts, or anything of that nature, which would causes hearing loss. Since I've been losing hearing since I was 5, they have practically ruled that one out because it makes no
The start of a new school year as a freshmen in high school away from my hometown. Everyone is anxious for this new and fresh start meeting new people and friends. I’m on my way to school very nervous and worried that they might laugh at me. As soon as I enter the class late, everyone stops and stares at me; I walk down the aisle to the nearest empty seat. I sat down quietly throughout my classes in fear that they might notice I’m a, “funny talker,” or that they laugh at me. Everyone avoided talking to me, seat next to me, or even do projects with me. I don’t have a contagious disease; I’m like every other ordinary girl in school. I work hard for my grades, I join organizations, I have no disability, I have control of my body, but I can’t control my stuttering. I’ve had this speech disorder since I was younger. I always had trouble making friends because I stress out and get anxiety trying
Overall, I have learned so much in English 111 and I have really enjoyed being in your class. Everything I have learned will help stay with me in my continuing years of college. I hope I have proven to you that the things you taught actually did help, and I gained so much knowledge about myself as a writer and a communicator. Your lectures were very interesting and you made them pleasant to learn. Thank you for a great semester.
Today is Tuesday, I was awakened by my brother leaning over me his cold fingers brushing over my unkempt hair, he whispered softly in my ear telling me to wake up.
Many people do not seem to be aware that there is a Deaf culture and many hearing people often assume that those who are hard of hearing desire to hear but unfortunately this is not the case. According to My Deafness – Deaf culture facts, (2015) “Deaf people often consider positives of being deaf such as
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.
In middle school I was diagnosed with a disability with the way I expressed myself through writing. Ever since, I have gained multiple values and learned several lessons about self confidence. I was taught to push past my limits, in order to be successful in reaching my goals along with my dreams. Today I am a senior in high school who was once thought to struggle, but was able to succeed beyond expectations. To some, a disability may seem like a setback from achieving goals, but to me I used it as a challenge for myself. I accepted myself for who I was and looked at my disability as a unique trait of mine. I was able to provide a message to others that anything you set your mind to is possible with dedication and hard work. It might take