(Ch. 60 of my storyblog of my journey into Deafhood…)

Deaf parents have been successfully parenting for ages. The majority of us have done so without adaptive baby care equipment or professional guidance. Being deaf does not prevent a person from becoming a parent. Nor does it mean that our parenting will be deficient or not up to standards. Hearing people should take note: We, deaf parents, learn quickly how to build on our personal and family strengths. We, as well as our spouses and children, learn to adapt.

For example, when my son was in his crawling stage, if my back was turned and I could not hear him cry or laugh, he would stop what he was doing, crawl or scoot over to me until he was in my view, and then once I could see him, he would begin to emote as he was doing just a moment before. Hearing children with deaf parents learn to adapt.

My son would also exaggerate his expressions to clue me in to what he was feeling. Babies with facially expressive deaf parents tend to be very facially expressive themselves. The children learn from birth that eye contact and facial expressions play a big part in the expressing and understanding of communication between the themselves and their deaf parents.

When my son was about 18 months old, he came toddling into the living room where I was folding some clothes. He tugged on my pant leg and began toddling toward the kitchen. I didn’t think much of it until he came back. He was trying to say something to me, but I couldn’t read his lips yet or understand his gibberish. I picked up on the fact that he wanted me to follow him, so I did. He led me into the kitchen and then pointed his finger up at the sink. I looked up and saw that I had left the water running! He was already alerting me to the environmental sounds around our home that I could not hear. I found that remarkable!

Today, Paul will still alert me to the microwave ding, the oven timer, the doorbell, or the phone, regardless of the fact that I have visual alert systems in place for these environmental sounds. He has just taken it upon himself to help keep me connected to my world. Though it’s not entirely necessary, it’s still pretty wonderful.

I began exposing my hearing son to sign language when he was a baby. He was signing before he was talking. All his babysitters were Deaf, native ASL users, or hearing people who knew and used sign language. I wanted him to continue to be exposed to sign language while I was away at work.

However, there were times when I got lazy and did not sign as much as I spoke with Paul. Being that spoken English is also my first language, I relaxed into this habit when I was at home, even though I knew it was not the best idea if I wanted to encourage Paul to sign. As a result, the sign language comes and goes with us. My bad.

For a while, my son struggled with a fine motor delay, which made tieing his shoe, holding a pencil, and signing difficult for him. Clearly, it was easier for Paul to speak than to sign. However, as he has become older, this has started to change. I am seeing him use more sign language with me because it has become more important for him to be understood. He will choose to turn off his voice and sign to me on his own.

With the advent of the TV cartoon program, Naruto, making hand signs has become quite popular among the boys at my son’s elementary school. My son’s exposure to sign language has put him ahead of his peers with the ability to make these hand signs. He prides himself on being one of the fastest “Jutsu” signers around our neighborhood!

Exposing him more frequently to my Deaf co-workers and their signing children, and taking him to more Deaf community family events, has helped him value signed communication. He is capable of reading some of the signs my Deaf friends use, but he is not always able to make the signs back. This has improved though with practice. This summer, I have been teaching Paul new sign vocabulary and he is now using signs and finger spelling more often. The key is to use it daily with him here at home. I use ASL all day at work. When I come home, I tend to switch over to using speech instead of signs. Again, my bad. This, however, is changing.

To his credit, Paul has become an articulate speaker, which I am most grateful for. He knows he needs to look at me when he speaks and to enunciate clearly so that I can read his lips. He has learned to be patient and repeat things for me when I am unable to follow and with encouragement, he will use his signs or finger spelling when I am unable to lip-read him. We laugh a lot at the funny things I think people are saying. Humor helps us all cope with my hearing loss.

Sometimes, Paul will ask my husband to interpret for him, as my husband knows and uses sign language. This works sometimes, but I prefer it when Paul signs or communicates with me directly rather than through another person. I try to make this a communication rule, relying on my husband to communicate only when the communication is urgent.

Eye contact has become another important communication rule in our family. Out of habit, my hearing husband and son also speak clearly and slowly while looking right at other people when they speak, whether they are deaf or not. Giving eye contact has just become a natural part of our lives. Eye contact is a wonderful interpersonal skill to have. It makes people feel connected. In the deaf world, the breaking away of eye contact is considered very rude. It’s like hanging up the phone or turning someone “off” so they can no longer communicate.

When my son was in pre-school, I remember having a parent-teacher conference where I had to explain our family dynamic of eye contact. The teacher said that my son would call out to her and tap her until she stopped to look at him. Only then would he feel satisfied and begin to tell her what he needed. She would answer him with her head turned away, but this wasn’t enough for Paul. He knew from our deaf/hearing family dynamic that communication only started once eye contact was given. After learning this, the teacher went from being slightly annoyed to being supportive and understanding of this occurrence.

As children with deaf parents grow, they begin to distinguish the difference in their parents and those of their friends. They recognize that one parent uses sign language to communicate and another doesn’t. They become aware when one mom responds and another misses the message. If I had hidden my hearing loss from others, my son might feel embarrassed that his mom was deaf.

But I have embraced my deafness, and my sense of deafhood has evolved over the years as I identify more and more comfortably with my deaf self. As a result, my son has actively joined me in teaching people what they need to do to communicate successfully with his deaf mom.

I have helped my son accept my deafness by sharing my story with our neighbors, his teachers, his friends and their parents. I began teaching all the kids in the neighborhood some sign language and made it a cool skill to have. I went regularly into Paul’s classes and taught his classmates different ways to communicate with deaf, hard of hearing or late-deafened people.

I even taught them how to sign some songs. One year, I lead Paul and his 3rd grade class in 2 signed performances of the songs Imagine and Beautiful Boy, by John Lennon for the school’s multi-cultural festival, with Paul at the microphone, and using ASL to introduce our family’s language of signs.

By embracing my deaf self and making it cool to learn how to sign, Paul and his friends were able to accept his mom being deaf, rather than tease or make fun of him because his mom could not hear. We continue to model and promote a healthy view of deaf people and the use of sign language in our home, in our neighborhood, and at Paul’s school.

(Footnote: You have been reading the final chapters in my summer storyblog entitled: My Journey Into Deafhood, which tells of the first recognition of my deafness and waking up to a world of silence, 26 years ago. It also tells of how I grieved, coped, adapted and then thrived as I learned to embrace my Deaf self. Thank you for reading! The final installment will show on August 8th, 2007. More coming soon…)

5 Responses to “My Journey Into Deafhood: Hearing Children of Deaf Parents Adapt ~”

    :) I am not surprised that a sensitive, thoughtful boy came from you and Brent.

    LaRonda,

    I love how you explained about CODAs (that is…if you refer your son as one) because now I can hold onto ideas that will help me in future when fatherhood arrives. a question: on top of what you just explained, what would be the top 10 (or 5) things Deaf parents should be aware of in raising hearing children? I love your telling tribute of performing signs in concert. :)

    Josh, I love this question and will take some time to think about it and perhaps make a blog post in response.

    ~ LaRonda

    I would like to tell you that it was a beatiful poem and an inspiration to me. I am having a hadr time I became deaf later in life. I am only 34 years old. I found out in high school I had 5 % hearing loss. As you know nothing can be done for that as time went on I k=noticed there was a problem. However, I blamed it on other people saying that they were mumblling. It was really me. I found out in 2002 that i was hard of hearing and I need hearing aids…then after 4 years of the in the ear hearing aids…I thought they were broken. I went to the doctor and audiologist and they told me the hearing aids were fine but I still could not hear with them. They tested me hearing and it ws worse. The dr. said if my hearing was as bad as it was I could not understand him. I told him I could read lips and get the idea. He said it was not possible. I knew that reading lips was not full proof but I knew enough. I found a new dr. I got new stronger (the strongest)hearing aids but gradually me hearing got worse. In july I had to have the frequency upped as high as it could go…then in september i noticed they were not helping things were not a clear. The audiologist said that could happen but she could not say for sure. My right hearing aid does not work at all. My left one helps but nothing is clear enough to understand. After I graduated from College I wentto the local community college to learn ASL to become an interpreter before I knew I had a hearing problem. Like I said I thought it was everyone else was mumbling. I had to have a physical to teach and I failed the hearing test in 2002 that was how I found out. Now that I have lost all of my hearing I am so happy I learned ASL. I prefer to use ASL then speak because I have noticed then people do not believe I am truly deaf. I have lost friends because i cannot talk on the phone….firiends I do have live so faraway and I cannot talk to them on the phone. I mean i can through the videophone relay and tty relay but ti is not the same. My problem is notw that I have accepted it…and a lot has to do with the deaf community that I have come to know…they supported me when I learned ASL and they continued supporting me and helping me accept loosing my hearing. I am writing to you becuase I am looking for help. My parents are hearing…I had to stop teaching because i could not hear the hearing students. So I became an assistant teacher for students who are deaf…I had to take a step back in order to take some steps forward…I am going to go to graduate school inthe summer for 6 weeks for 3 years to get my Master’s degree in teaching students who are deaf. My problem is that people that have known me growing up and even for 10 years have known me as hearing. My mom is trying to learn ASL but my other family is a different story. My father refuses to let me relay him. He hangs up. I have known one person for 10+ years and I know at first I was hearing to her but now she gets frustrated when she is calling me and I do not hear her. She is a Sister that is the supervisor for the Deaf apostolate for my church. We are very good friends but what upsets me is that sometimes I feel like she does not accept me any more. She tells me all the time that there are better ways to communicate then using the relay or using the VP which she has. I emailed her a long email one day saying you have no clue how hard this is for me. You get frustrated but how do you think I feel. I am frustrated when people do not believe me becuase I have a good voice. I get angry when people who I am close to get frustrated when I do not hear or understand them. She told me she understands…I said you can never understand until it happens to you. My mom gets frustrated as well…she also says if it is frustrating for her it must be frustrating for me. I told her too you will never know or understand how frustrating it is for me…she says she does but I said you don’t because untill it happens to you you will never ever understand…I can’t talk to my friends when they call you have to talk and translate for me the best you can. Two friends will accept the relay and so will my mom but I am so angry. Do you know of a book or something I can read to feel comfort about how other people feel when they lost their hearing. I am only 34 so the books I have seen are for people who lost it with old age. I am not old and I am scared. My friends who are deaf accept me as culturally deaf because they have known me for more the 10 years now and because they were my influence and support when I was learning ASL. Why is it so hard for people to understand that it is not about them. I have tried to called Drs. offices my self anf they refuse the relay so who do I have to have call my mom or a friend. Sometimes the teacher where i work…I am her assistant she became such a good frined since I have meet her in August…we have similar personalities…she is not deaf but she has even had to make calls for me. Is this what it is like to be deaf and not be accepted or is it because i have lost my hearing recently. I feel like I am on a fence…tilting one way to hearing and one was to deaf culture. I am scared and frustrated. I want people to accept me. So many people have said oh I am so sorry it is ashame. I do not see it that way. I am me and I cannot change that…I love who i am. Now I have people telling me to get a Cochlear impant so I can be fixed. I refuse…i do not like the idea nd I feel I do not need to be fixed. Is that wrong becaue i am thinking about myself and not other people and what is best for them in order to communicate with me. I also know that a cochlear implant is not a guaranteed fix and if I had it done and it does not work then I am stuck with some chip in my head for nothing. Cna you give me advice? I know other people who really do not want me to go through the surgery of the CI…please if you know of any books or advice you can give I will be happy to have it. I want people to know I am not diffferent i am still the same person but with a different way to communicate now. I am sorry this is so long but you seem to be so confident…I have talked to my friends who are deaf but it is hard becasue they are close with the sister that is my friend and other people. They tell me it will take time…Anything suggestions would help. Thank you…oh I love the quote you have from Saint. Benedict…

    Maureen,

    Bless you, Dear One. I’ve been in your shoes. Thank you for your sharing.

    I invite you to view my entire story of becoming Deaf.

    http://www.earofmyheart.com/wordpress/2007/07/13/want-to-know-how-i-became-deaf-ch-1/

    It is my story blog. I believe you will find solace and advice there.

    I also encourage you to check out http://www.alda.org for ore information about support to Late-deafened adults.

    I welcome your ongoing dialogue.

    ~ LaRonda

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Copyright 2006-2008 by LaRonda Zupp