Hey, My name is monica and i am attending WSU. im interested in doing an interview on growing up deaf and understanding some experiences. if you're interested email me at mons_40@hotmail.com or let me know on here.
Here are some questions
How old were you when people first found out you were deaf?My mom found at age 3 that I had a profound severe hearing loss.
Did your parents share their reaction with you when they found out?Mom tackled it head on. She worked for 7 years to have doctors fit hearing aids one me. Mom didn't have a negative reaction.
Have you ever noticed differences in dciplining in siblings?Nope. I am the middle of 3 girls. My mom is hard on all of us.
what is your education background?B.S degree in Early Childhood Elementary Education/History, M.S. in Special Education
Where do you work? Do you like it?Special Education Teacher for a local school system. I love it.
ARe there communicaiotn barriers at work?of course. There are barriers everywhere. I have an amplier phone. E-mail is the favored for of communications. My school system is very welcoming and understanding.
Is there fair promotion advancement?Yes, I was selected for my current position even before I finished my degree.
Are there any other deaf employees?Guidance Counselor is hard of hearing. the computer lab teacher is deaf. Her mode of communication is ASL.
HOw do you communicate at work?I am oral.
Do you use a hearing aid and if so what is your experience with it?I wore a hearing aid for 27 years. I did benefit earlier in my life. My hearing is progressive and around 7 years ago my benefit began to decline.
How old were you?When I lost my hearing - either at birth or age 3. We don't know the details. I am trying to find out.
Do You have cochlear implants?Yes, bilateral Advanced Bionics since July 19, 2007
Do you encourage others to try?To try cochlear implants? Depends on the person. I let others know it is a personal choice and my benefit is the same as they will have.
Do people communicate differently when they find out you are deaf?They use to before my CIs. My fellow teachers use to make sure they had eye contact and not yell down the hallway to me. Just a respect of me.
if you had a deaf child what school would they go to?Up to my parents.
Do you have any suggestions at all for improvements?respect and understanding.
Where do you go for help?Help???
How do you feel about the services for the deaf where you live?I have not used any services here in my town. I used disabilities services at the local college. I know we have league of hard of hearing and deaf located in my town.
iHere are some questions
How old were you when people first found out you were deaf?
3 years old
Did your parents share their reaction with you when they found out?
My parents were very accepting of my hearing loss -- especially my mother who made sure my needs were met in school (i.e. front row seating, etc.)
Have you ever noticed differences in dciplining in siblings?
No. My parents were strict raising my sister (hearing) and I.
what is your education background?
Attended public schools in a mainstreamed program; am currently in my final year of study working towards a Bachelor's degree in social work.
Where do you work? Do you like it?
ARe there communicaiotn barriers at work?
Is there fair promotion advancement?
Are there any other deaf employees?
HOw do you communicate at work?
Do you use a hearing aid and if so what is your experience with it?
I wore hearing aids from age 15 until the time I received my first CI (December, 2004). When my hearing loss was moderately-severe, my experiences with using hearing aids were beneficial. When my loss reached the severe-profound range, I used an FM system for 6 years until speech discrimmination was no longer possible. From that point on, I began to learn alternative communication techniques for the deafblind and later received CIs.
How old were you?
I was 3 years old -- although my former hearing aid audis believe my hearing loss/deafness may be congenital given the fact that newborns weren't given hearing screenings in the late 60s/early 70s.
Do You have cochlear implants?
Yes. A Nucleus 24 Contour Advance (left ear) and a Nucleus Freedom (right ear) both manufactured by Cochlear.
Do you encourage others to try?
If someone asks me questions about CIs, I am happy to share my experiences. However, I do not force my decision to be implanted on others. If a person chooses to receive a CI, great. If they do not, that is okay too. Making the decision to receive a CI is a personal one.
Do people communicate differently when they find out you are deaf?
Yes. Prior to receiving my CIs, people used a variety of communication methods with me including tactile sign (PSE, SEE or ASL), print on palm (tracing block letters into the palm of the hand), TeleBraille (Braille TTY), Teletouch (a typewriter-like device with a QWERTY keyboard on one side and a single Braille cell on the other; when a key is depressed on the QWERTY keyboard, that particular letter appears on the Braille display), typing information in MS Word or Notepad so I can read it on a Braille display, Braille/raised print alphabet card (where my finger is placed on individual letters to spell out words), Screen Braille Communicator/SBC (a device that works similarly to the Teletouch except that it also has an LCD screen for sighted-hearing and a Perkins/Braille keyboard for input), Braille realtime captioning (a captionist's laptop is connected to my BrailleNote -- a PDA for the blind -- information typed by the captionist appears on the BrailleNote's Braille display) and Fingerbraille (tapping out letters of the Braille alphabet on one's arm, lap or back).
if you had a deaf child what school would they go to?
I would initially place them in a school for the deaf so they can learn ASL. Once they've mastered ASL, I would transfer them to a mainstreamed program in a public school setting.
what method would you use? ( oral, speech theropy)
ASL and oral (provided that my child isn't having too much difficulty learning how to speak...If my child were struggling a great deal with oral/speech therapy, I would remove them and place full emphasis on ASL communication.
Do you have any suggestions at all for improvements?
Where do you go for help?
After my hearing loss reached the severe-profound range, I attended my local deafblind center to learn alternative communication techniques. Once that training was completed, I no longer required any assistance from others (with the exception of using an SSP for shopping and other errands) because of my deafblindness.
How do you feel about the services for the deaf where you live?
While I've never used their services myself, we have a Center for the Deaf and Hard of Hearing which provides sign language classes, early intervention programs for deaf/Deaf/HoH children, audiology services, etc. I've been told by many of my d/Deaf and HoH friends that the services they provide are excellent.
Here are some questions
How old were you when people first found out you were deaf?
Did your parents share their reaction with you when they found out?
Have you ever noticed differences in dciplining in siblings?
Where do you work? Do you like it?
ARe there communicaiotn barriers at work?
Is there fair promotion advancement?
Are there any other deaf employees?
HOw do you communicate at work?
Do you use a hearing aid and if so what is your experience with it?
Do You have cochlear implants?
Do you encourage others to try?
Do people communicate differently when they find out you are deaf?
if you had a deaf child what school would they go to?
what method would you use? ( oral, speech theropy)
How do you feel about the services for the deaf where you live?