Life in progress

At a Loss for Words

19 Comments

Where’s your communication book? I’ll ask your teacher to tell you.

It’s the most common phrase that is signed in my household, aside from, I love you, and Go to sleep already.

The problem is, of course, that my son Alex doesn’t ‘speak’ the same language as I do, and sometimes I’m the one at a huge disadvantage. I, whose life consists of putting words together to make meanings clear, am unable to communicate with my own offspring. What kind of sick force in the universe came up with this irony?

Tonight I had to try to explain to Alex why he wasn’t able to eat from my plate. It’s something that I allow him to do on occasion–not something I allowed my other two sons to do–since he doesn’t eat much more than one piece of anything, being that he’s tube fed. But now, since I’m not sure I’m completely over this bug, it’s a no-no. Germs are not something I often talk about, and so once again I’m faced with my lack of knowledge, and my incompetence in being fluent in American Sign Language.

Can you fathom the frustration at not being able to say the simplest of things? With a hearing child, the conversation would be over in four or five sentences. “I’m sick, and if you eat from my plate you might get sick. Why? Because there are these things called germs – tiny things like bugs crawling around in my food. You still want some? I thought not.”

Instead? It’ll have to wait until tomorrow.

Don’t get me wrong – I’m grateful that I have the resource of the Deaf school to back me up when I need it, and especially that they are teaching my son to communicate with his peers. What scares me are the stories I was told by a few different Deaf people of their hearing families – that they grew apart. The Deaf have their own community. In fact “Deaf” is capitalized when the word is used to describe a person in the same way American is – because it denotes that very community.  It’s only by virtue of the fact that Alex has a global intellectual delay that I might have to care for him well into adulthood.

In the meantime, I’ll keep trying to learn his language. Because once he’s twenty-one and has to leave school, I won’t have a communication book to write in. And I’ll be at a complete loss for words.

Author: Linda G. Hill

There's a writer in here, clawing her way out.

19 thoughts on “At a Loss for Words

  1. You are truly inspiring for so many mothers Linda. 🙂

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  2. I imagine that it is highly frustrating at times, but this also shows that you’re a great mother. You use the tools you’ve been given and that is a wonderful thing.

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  3. I’m pretty sure frustrating doesn’t cover it for you – it would be difficult.

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  4. What a scary thought… to be without the words you need to express something to your loved ones. As an ESL teacher, I can understand a lot of the frustrations (my students are typically in the 4-5 age range, and know no English when they start), but I hope your fears––that you two will grow apart because of the community––never come true.

    Keep working at it; by the time he’s old enough, it’s more than likely you’ll be fluent! You can make it happen. 🙂

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    • I suppose if anyone can sympathize it’s got to be an ESL teacher. It’s like immersion; I’m the one immersed and he’s the teacher. But of course, he only teaches me what he wants me to know. Unfortunately there are no courses to be had in the area, so it’s a very slow learning process. But as you say, I’ll get there.
      I need to start my own dictionary.
      Thanks very much for your kind words, Alex. 🙂

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  5. This is a beautiful post. You sound like an amazing mum to Alex. He is blessed to have you.
    And I love how he puts his hands over his eyes. How cool is that!

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  6. I found that strange about the deaf community. Don’t get me wrong, I understand it’s a difficulty, but there was one college that when a new technology was announced which could cure several forms of being deaf, they fought back and said they don’t want to hear. Keep him close. Love him. You’ll be fine 😉 It sounds like you do a lot for him, and I doubt he’s going to forget that.

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    • It’s true, the Deaf community is very protective of its culture. The way they see it, they’ve been able to make lives for themselves just as they are, and in many ways, asking them to give that up is like telling them they’re ‘abnormal’ to be the way they are and do things the way they do them.

      Thanks for your support, Paul. And for caring. I appreciate it. 🙂

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  7. Life does have its way of presenting this challenges, doesn’t it? What can we do but face them, hopefully with the support of family and friends?

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    • Exactly. Face the challenges and do my best – it’s what I’ve done since their dad and I broke up, and it’s what I will continue to do.

      Family, friends and thank goodness, teachers.

      Thanks for the moral support, Nav. 🙂

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  8. What courage. My niece has a deaf child and I know how difficult it can be. But also she has told me that her daughter sometimes uses her deafness to tune out what she doesn’t want to deal with. Smart kid 🙂

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