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Experience with hearing loss
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Every day for the past 2 years I think about why I lost my hearing. My life changed dramatically that day. My hearing loss has been a big impact on my life. I remember the day because it was my sons 11th birthday.
That morning, I began my regular routine; cooking, cleaning and setting things up for my son's birthday party. I began to feel pressure in my ears like if I was on a plane that reached a high altitude. By that evening my ears were blocked and the sounds around me were very faint. I was like a hypersensitive sound. I went Kaiser a couple of days later to try to get a walk-in in appointment, but instead received an assumption that I had wax build up, and was advised to buy a wax removing fluid. As days went by and I had no improvement I rack my brains on what could have happened.
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Spending time with my family became harder to do with; with them asking questions, engaging in conversation with me, my son would call my name, my phone was ringing, but I could not make out what anyone was saying or hear my phone.
My hearing loss was overwhelming. It really was hard on me because not hearing my son was something I could not comprehend.
I was stressed and overwhelmed with anxiety. I was panicking and felt isolated. How could I possibly be a mom with my hearing as diminished as it was? I sobbed with raged and sank into a deep depression as the days went by. So I went to the emergency room where they implied that I had fluid buildup inside my ear and could have been from a cold I had or allergies. And was told to go home and let the fluid dry up, which could take up to 3 months.
The thought of not hearing for 3 months was overwhelming for me, so I visited an ear, nose, and throat doctor 2 weeks later. And they check my ears and found no fluid inside, now I'm confused. A hearing test confirmed the worst. I was told that hearing was gone and hearing aids would most likely not help. What made it even harder was that they said my hearing never get
better. I struggled every day, pretending to myself that the doctors were wrong. I’m a not a good lip reader, which made it even harder for me. I am so clueless about my hearing loss. I was embarrassed to have lost my hearing at such a young age. I hide my hearing aids and I try my hardest to make out what is being say to me. It's even hard on my family because it is just as new to them as it is to me. When I think about my impairment I get a great deal of sadness. When I have to go out and conversing is required I have to bring my son just so he can repeat was said to me. I have encountered people that become frustrated because I constantly have to ask them to repeat themselves. It's as if no one understands me when I tell them I am hearing impaired. I guess they assume that all hearing-impaired people have no speech as well. It is still taking my family time to accept the fact that I can no longer hear as well as I did. I seem to always get "Oh never mind you can't hear me" I find myself engaging in conversations less and less every day, because I become more depressed that in a matter of hours I went from hearing everything to hearing nothing. And as of today, I refuse to believe that this is permanent. This misfortunate has truly impacted my life, but I refuse to let it define it.
Mark started losing his hearing when he was about six or seven years old. This was manifested in confusion in music class, misunderstanding the words that the choir was singing, and discombobulation in noisy rooms. Eventually, it was noted that Mark’s hearing was deteriorating.
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
These symptoms include: two or more episodes of vertigo lasting approximately 20 minutes each, tinnitus (ringing or buzzing of the ear), temporary episodes of hearing loss, as well as a feeling of “fullness” in the ear. In terms of assessment, the NIDCD asserts that some physicians will implement the use of hearing tests to determine the extent of the hearing loss that has occurred due to Ménière’s disease
Finding out about my grandmothers death was the saddest moment in my life . I didn't understand . I didn't expect it to happen , not to me . I wondered why god had taken an important person away from my life , ad for that i felt confused and miserable . I cried for hours that day . Nothing could have brought me joy that day but the presence of my grandmother , but she was gone and i found it hard to overcome the situation.
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.
Being the second oldest of eight children, there was never a dull moment in our house. Personality differences were common but the love we had for each other was obvious. With this being said, I am the only child out of those eight that has not only graduated high school but I am now working towards my Bachelor Degree in Elementary Education. We were a poor family and education was not on the top of the list of priorities. The first four of us were like stair-steps and seven years later came another set of stair-step children. My closest sister, Evie, was deaf and my mother sent us both to a school for the hearing impaired to ensure someone could communicate with her. I have fond memories of this school and the time Evie and I were able
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
Hearing loss affects approximately 17 in 1,000 children under the age 18. However, it is more common in older adults. Approximately 314 in 1,000 people over the age 65 have hearing loss issues. Hearing loss can sometimes be fixed but other main types of hearing loss can not be fixed. Hearing loss is a serious subject that affects many people throughout the world, young and old.
Hearing loss and/or hearing impairment occurs when there is an issue with one or more parts of the ear. Someone who has hearing loss may be able to hear some sounds or nothing at all. About 3 in 1,000 babies are born with hearing impairment, making it the most common birth defect (Morlet 2012). There are ways to determine if your child has a hearing impairment at birth, not to prevent your child from having a hearing impairment, but to determine if there is a possibility that your child may have the most common birth defect. Newborn hearing screening focuses on identifying hearing loss early (Listen 2013). In other words, if a newborn were to get a hearing screening shortly after birth, then there would be less percussions than if the parents waited to get a hearing test later on.
Congenital hearing loss is described as hearing loss that exists at birth. Factors responsible for this condition include those present during pregnancy (such as hereditary factors), as well as factors present after pregnancy. An inherited congenital hearing loss could be conductive, sensorineural, or even a combination of both. The amount or progression of this type of hearing loss varies according to each individual’s case. According to Richard Smith, congenital hearing loss is “syndromic (associated with malformations of the external ear or other organs or with medical problems involving other organ systems) or nonsyndromic (no associated visible abnormalities of the external ear or any related medical problems)…” Over 400 genetic syndromes are associated with congenital hearing loss. These include Treacher Collins, an autosomal dominant disorder and Down syndrome, an x-linked hearing loss. Although congenital hearing loss can be difficult to live with, hearing aids, surgery, and therapy are all available as forms of treatment. Hearing loss must be treated as soon as possible to prevent as many delays in the child’s language development as possible.
I was born deaf, but my parents don’t know until I was a little under two years old. Good thing that now the technologies and ear doctors/specialists in medical field are catching up to analyze the baby in order to inform the parents about their infants’ hearing level. It is known as Early Hearing Detection and Intervention aka EHDI. Early Hearing Detection and Intervention program is “a process of identification and intervention for newborns with congenital hearing loss.” The meaning of EHDI is very medically and I remember that we discussed in class about medical and deaf terms and how it can be very scary for both deaf person and parents. The terms are range from hearing loss to intervention. The doctors should tweak the medical terms and approach to parents of deaf child to make the situation less extreme as it sound. Those terms tend to affect the parents’ decision because they feel rush and overwhelm by it.
An 11 years old kid lying on the ground in a dark room crying, shaking, and trembling with intense pain in both of his ears. The pain was similar to as if someone was hitting with some sharp object inside his ears and every time he would feel the shock of pain, he would pull both of his ears while enduring the pain. The pain would raise every couple of second and with each shock of pain, the kid would lose part of the hope that he had of surviving. He would experience so intense pain that he had never anticipated and all he could think of that “he is about to die.” This was the experience that I felt when I had a severe ear infection in both of my ears.
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
My instructor had informed us about people with hearing impairments and disorders, but I never thought much about it. After this assignment, I realized how hard it is to have your hearing impaired. I had the luxury of being able to take out my plugs and fix my impairment if I became to overwhelmed or stressed. Those who are impaired do not have such luxury. I did not expect as much of a psychological element to this assignment as there was. There were times where I felt anxiety stirring inside of me. I became anxious if I missed something. The first day back with un-impaired hearing was memorable. I kept thinking to myself how hard short conversations would be if I was impaired. Moving forward, I have a better grasp of what hearing impairment really is and how hard it is to live with. I will be more conscious of my hearing because I never want to experience fulltime