How I feel about Deafness...
Here my thoughts on deafness… It shouldn't
define who I am. It shouldn't be a prideful thing. Yes I am deaf but only for a
short while. I should be working towards defining myself as a daughter of God.
Yes, I am happy and should have a good attitude while working through this
physical trial that I have been given. I was given this trial to learn how to
see overcome obstacles that deafness has given me. Deafness does not define who I am. I am a
person who loves my family. My family helps defined who I am. Not only does my family but my friends.
Deafness is only a small part of who I am.
My story…
I was born hard of hearing. I was born with my left ear completely deaf
and my right ear with a 30 percent hearing loss. I was finally fitted with a hearing aid when I
was three. My parents decided that it was best for me to learn how to talk than
signing. They felt it was best because of how much I could hear. I went to the
Deaf and Blind school in Utah for a year. There I learn how to talk and have
good speech.
My parents decided to pull me out and do home
school. To this day I am so grateful for my mom for teaching me how to read,
write, and talk. Not only did she teach me all the academic stuff but she
taught me that I can do whatever I wanted to do. She did not tell me I could
only do certain things. She had me do piano lessons and encouraged me to learn
to play the flute.
When I was 16 I became lifeguard and a swim
instructor. I struggled with getting that job because I was hard of hearing.
They were concern on how a hard of hearing person can hear the whistle or a
person who is struggling. I told them to give me a two week trial. After that I
became the best lifeguard they ever had.
When I became 18 I was having a wonderful
year. Until I notice something different with my hearing, it became quieter. I
notice the piano sounds different. I notice my family voices did not sound the
same. I had just gotten a new hearing aid. I felt like it wasn't working. I went to the audiologist they figured it out
they compared my hearing test and found that I had lost hearing. I went from 30
percent to 80-85 percent lost. I was in shock. Lost for words.
That day driving home from the audiologist
was really hard and a blur. I don’t remember talking much with my mom. I
remember being really annoyed that I couldn’t hear what I wanted to hear. I
remember feeling like what am I supposed to do.
I was running question after questions through my head. For example, how
did this happen, why is this so sudden, why now? Etc. I felt so alone. Because I
knew my parents had no idea what I felt like.
My parents and I began to do some research
on Cochlear implants. Not only that they were trying to track down my favorite
audiologist that I saw since I was 3 years old. I was seeing doctors after
doctors. I was getting sick of it. I hate going to doctors. We went to Cochlear
implant doctors asking questions. We
were trying to figure out what the next step would be.
At this point I had given up playing the
flute, the piano and even the guitar. I had acted like everything was okay. I
shut everyone out about how I was feeling inside. I was not happy. I was sad.
Everyone around me was trying to make accommodations for me. I acted like that
was okay but really inside of me I felt like I had lost my independence. They
were trying to do what they felt was best. Not only was I shutting people out.
I lost friends. I became different to them. Most of all I think they didn’t
know how to interact with me because I couldn’t hear as well as I used to. I
wanted to scream and shout but I didn’t know how. I was lost.
Luckily I found this great audiologist who
cares about his patients. He found a great hearing aid that worked perfectly. I
was still considering an implant. I applied for one with my insurance. My insurance
turned me down. I was frustrated as to why they would do that. However, the
more I got used to this hearing aid I had the more I realized I did not want
cochlear implant. I didn't want to have to retrain my brain on how to speak. I
hate speech therapy so why would I want to go through that again. Not only that
I had a fear. That fear was if I do the surgery there is a potential that it
might not work and I have lost all the hearing that I currently have. Plus it didn't feel right to have one. So I
decided not to get one.
I am not against implants at all. But they
are not for everyone. Everyone has a choice and I chose not to get one. Eventually
I started taking sign language classes through the community. I wasn’t really
learning much. I really wasn’t using it much because I had not practice.
In 2005 I decided to make a move. I moved
to Buffalo, New York. I wanted a new start. I wanted to find something new. I
did. I found a school NTID: National technical institute for the Deaf. I did a
tour with my Aunt. I felt at home the minute I touch campus. I met teacher that
were signing. I met some students who were going through the exact same thing
as me. I felt like finally I met people who understood.
I was learning how to sign, I had deaf
roommates and I had deaf teachers. For the first time I understood math because
it was visual language. However, I became confuse again. Who am I? I am in a
world that has a culture. At first I didn't know who I was. There was all this
talk about identity how I should introduce myself etc. Slowly I began to accept
that I am Deaf. I was happy. I felt normal. I didn’t have to hide anymore. I
felt home. I felt like I was free because I felt secure in learning ASL to be
able to communicate.
Elizabeth, this is wonderful! Thank you for sharing this! I wasn't aware of all the hardships and adventures in your life, and I'm excited to learn more. Love you!
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