
The earphones are tight and the chair is tall, so tall my feet dangled in space.
I am in a booth, a plain one, tan, four walls and one window, that’s it. They could have at least hung a poster.
I hear a noise in the earphone, he is speaking, the doctor that my parents found. He has a funny mustache, all curly on the ends. I don’t know what he is trying to tell me so I sit still. They will tell me again if it is necessary.
The words make sense this time; he wants me to repeat anything he says from now on.
I nod.
I can see him in the window now with a microphone.
He waves.
I wave.
I hear something.
Is it a word? I try to figure out what he is saying. It is like a puzzle sometimes. I listen carefully, I am close to it, but another word comes. I try to form this one and lose the first one, my head hurts.
I am going to sound stupid if I don’t speak soon. He repeats it, this time I hear it. “Hotdog,” I say aloud. I am happy, but no time to rejoice as another word comes. I try to form it on my tongue, I can’t.
I begin chewing my lips. I do this when I fear failure. My fingers tuck a loose strand of my hair from my ponytail behind my ear.
“Superman,” I repeat. The funny tingle runs through me again. Then a few more words come, they are clearer. I can say them now.
My eight-year-old mind scrambles to keep up again as parts of the word fades. Parts no longer coming through again.
Why do they go away sometimes?
My blue sneakers bang against the stool legs as metalic sounds vibrate out and tease me.
I know some sounds are words, but they hide from me, just giving me little bits to let me know something is there.
The man opens the door and I look to him, he doesn’t speak now, the adults always stop talking after awhile.
He waves his hand for me to come out.
I am relieved to be done and yet scared that I failed something, someone.
He hands me a lollipop. I am embarrassed but take it. I’ll give it to my little brother later.
My parents come in and I can leave now.
The door closes and I walk over and sit in a chair.
I look around; the walls are bare, except for a window. I look beside me and an older lady is there, she is talking to me I think, I nod as I chew my lips and my feet bang against the chair legs.
*******************************************************************
Reflecting on this memory I remember how things were small and confined in my world. I was between the hearing and deaf world, and without technology I would have been lost to it, but the results came back and the doctors found that with some minor operations I would be able to hear normally, with the exception of a few tones.
In school I was cooperative, kind and labeled a daydreamer. One of the teachers moved me to the front of the class and took note that I wasn't hearing many things. This was how my loss was discovered.
My dad felt bad, he is hearing impaired, his one ear has always been deaf from childhood and his right is no where perfect so we learned to talk in louder voices at home, thus my deafness was not discovered.
I can recall that after the operations the world was filled with all these missing sounds. Bees did buzz, refridgerators made a hum, fans a whirr and jets high up were actually not soundless. I spent many of my waking hours finding the source for new noises, right down to someone chewing gum nearby.
I still struggle some as I have some hearing loss to this day, minor infractions really. I have 75% of my hearing after years of operations. I had a relapse in my late 20's where I lost my hammer in one ear and half of my tubes closed in the other, I lost the ability to talk on the telephone for 6 months, but corrective surgery brought most of it back. I can only be grateful.
I think I get my attitude from my dad, he never made his hearing loss an issue in his life.
I will put on caption with my television, my father won't. He insists on just turning it up louder.
Once when he visited he had the volume at an extreme rate, I came in and said "dad, can you hear it?"
He says, "I like this movie but I can't understand it." I then informed him that he had it on a spanish channel.
He says, "Well that's okay, I seen it before," and continued to finish the movie at the same rate.
I never knew when I was saying, "Can you hear me now?" that I really was saying, "Can you hear me now?"
When I talk to your Dad, I should say REAL LOUD, "NO HABLO ESPANOL!" but he's probably heard that before.
Seriously ... very touching piece ... just playing, you know!
Huggggggggggggggggz,
Taylor
P.S. Don't forget ... Dawn Dishwashing Liquid cures POISON IVY!
I appreciate your kind words.
ice
Its true, we should appreciate what we have in senses. The lack there of doesn't make a lesser person either. You are right, it is important.
LOL
You are too funny.
You know I am going to have to play on that from now on when we talk!
Dad is a riot isn't he?
Don't ever stop joking around, you are one my favorite playmates!!
(besides, if you behave, then I will have to behave too)
Its amazing how we learn to cope.
Bob H
I was raised to not see things as a 'problem'. My dad had a hearing issue, and I had a hearing issue. If I concentrate on the things wrong or see these types of things as a problem, then they are one. I know some deaf friends of mine that function in life very well.
I think the thing to realize is that we all have our 'things to deal with' but don't make them an issue, figure out how you can deal with it and move on.
For instance, my middle child has dyslexia, we have to figure out how to make it work for school, but the beauty of dyslexia is that the most creative people who walked this planet is dyslexic. That means that my daughter is highly creative. (I also have dyslexia )
I have a blog about it in my archives.
She is considered learning disabled by school's standard. She is an amazing artist in life's standard. We concentrate on that, she will be just fine.
I am very ADD, I learned I had it, read what triggers I should be aware of and figured out how to function with it. It works for me.
My youngest takes edicine on school days as she has it as well but I am teaching her the coping techniques as well.
With a hearing loss, having dyslexia and ADD, I could sit on my hands and whine and mope or I can get a good tutor, study up on things and move along. I chose the latter, it's all up to us.
Its funny, I have ADD and so much of my childhood seems to be skattered images, like leaves in the fall in the woods and I wonder to which tree they belong.
But some memories are vivid, this one is like that.
I love how I was raised, my family stay full-bore-ahead and don't focus on the negatives, but when I had the operation, the day I went to go home, hit my parents in the gut. I stood outside the hospital and couldn't move for a while, there were so many new and unusual noises and I was trying to decipher and place them all.
I like sharing here. It seems a soft background to prop against, you know?
I didn't find your comment offensive anymore than I was trying to correct you. I was explaining how wehandle things in my family is all. Nothing you said was wrong or taken that way.
So cheer up girlie!
Love how you expressed yourself it this writing.
Being the parent of a child who became deaf at age nine, I can empathize with you. I hated that tiny cubicule of a room, filled with dotted holes in the ceiling that they placed him in. I hated that they wouldn't let me go in with him so that he wasn't so scared. It angered me that even though he couldn't repeat the words back to the person in the correct manner, the test continued...making my son feel like a failure. I wish this was one area that I could say that things have improved on in their techniques of adminisistering these tests but it hasn't......it's all pretty much the same. I'm sorry you had to go through that.
(P.S. did you get my pm)?
thank you for this insight into your life and also the insight into the life of a person who lives with these kinds of issues. reading your blog and CMs comment gave me a new appreciation for how blessed I am,
I think some of my teachers thought I had hearing loss in junior high. I was sent to an audiologist - but she declared me ok. so maybe I just had a certain teacher deafness
A most poignant memory, vividly recaptured. Not so strangely, I have found my hearing fading as I grow older. Strangely, I have suffered tinnitus for as long as I can remember and that danged noise is as loud as ever.
The funniest thing is that I feared that teacher, she was the roughest one I ever had but she did notice and was a big help in a time of need.
Amazing what medical science can do.
Thanks
We can be so amazed at the miracle of science and how far they have come. Without them I would be deaf today, not that I wouldn't have managed, but it is easier with my hearing.
I am glad you found the strength as well.
Thanks
Did you get my reply?
Too funny, I think we all suffered that wih certain teachers, I am sure.
It is a blessing to appreciate things that at times are taken for granted.
It has, I hope yours has been as well.
I have heard that tinnitus is terrible to deal with, my heart goes out to you.
I thought you were gone, I am grateful to find myself proven wrong.
I am visiting and book marking you again.
It appears that you have great coping skills.
PROFILEFANTASY.COM
Thanks, I never seen it that way. I have to actually remember I have to cope. Which makes me giggle because many others never forget for me.
I can mope which accomplishes nothing or I can adapt and move on in life.
This is going to be fun!
You deserve it, you are a great mom.
I hope you have an awesome Mother's day!
I was raised to not see things as a 'problem'. My dad had a hearing issue, and I had a hearing issue. If I concentrate on the things wrong or see these types of things as a problem, then they are one. I know some deaf friends of mine that function in life very well.
I think the thing to realize is that we all have our 'things to deal with' but don't make them an issue, figure out how you can deal with it and move on.
For instance, my middle child has dyslexia, we have to figure out how to make it work for school, but the beauty of dyslexia is that the most creative people who walked this planet is dyslexic. That means that my daughter is highly creative. (I also have dyslexia )
I have a blog about it in my archives.
She is considered learning disabled by school's standard. She is an amazing artist in life's standard. We concentrate on that, she will be just fine.
I am very ADD, I learned I had it, read what triggers I should be aware of and figured out how to function with it. It works for me.
My youngest takes edicine on school days as she has it as well but I am teaching her the coping techniques as well.
With a hearing loss, having dyslexia and ADD, I could sit on my hands and whine and mope or I can get a good tutor, study up on things and move along. I chose the latter, it's all up to us.
Such an amazing comment... such profound thoughts... if only all children were raised by such loving hearts
Your children are truly blessed to have you as a mom.
I am glad for the compliment. I will remember to thank my dad for my attitude,because that is from where it derives.