Yes You Can! How to encourage your blind child without pushing too hard

"Devastated."

I hear that word a lot. "When we first discovered our son was blind we were devastated..."

I understand that. I've experienced it myself. But it's funny how, now over two years after the so-called devastation, it's so hard to imagine that I ever felt that way. My son Ivan just seems so perfect and so full of potential and possibilities.

But there certainly was a time when all I could think about were all the things Ivan would not be able to do as a blind child. He'll never blow bubbles, fly a kite, or watch Sesame Street. Probably because coloring was always a favorite activity for me as a child, I kept returning to the thought that he would never color in a coloring book. How could a blind child possibly have fun with colors?

Eventually I realized that I was really stuck in the world of can't, so I began trying to think more positively. I started to say to myself, "Ivan can do anything he wants to do!" He can color, fly a kite, go to the movies, play sports, and whatever else he puts his mind to!

This is a much better attitude, but it also has a dangerous down side that I almost got caught up in. It's hard to remember that it's possible to be too positive. Not only will Ivan definitely face limitations, I also risked pushing him into activities just for the sake of proving that my blind child can do all that a sighted child can.

I suddenly pictured myself forcing Ivan to play soccer or color in that coloring book just because that's what all the "normal" kids are doing. It made me shudder.

I didn't want to foster the attitude that Ivan can do things simply because I desperately need him to. I see this with parents of blind children every day: They push their child to fit in or to participate in activities that don't interest them simply for the benefit of the parent. I think it's very important to remember:


My child will do what he wants to do because he wants to do it or because it benefits him in some way.

Now I try to be more realistic in my expectations of Ivan. With coloring, for example, I still think that this is something Ivan can do, but now I think about how we can make the activity as entertaining and beneficial for him as possible.

Activities like coloring and painting are good for Ivan because they strengthen his hands, encourage grasp, and facilitate wrist rotation. They're fun because there are more elements to coloring and painting than just the visual; crayons and paints, for example, have a distinct smell and feel.

Also, since Ivan is blind, we can experiment with different ways to make coloring and painting exciting for him: We can finger paint with pudding, then eat our art; we can draw with scented markers; we can place sandpaper under our drawing paper so that the crayon marks are raised; or we can make art with strings, buttons, curled lengths of paper, and other three-dimensional objects. Whatever we do, it will be beneficial because we will explore Ivan's other senses while encouraging him to participate in those "normal" childhood activities. And most importantly, it will be fun because we'll only do it if Ivan finds it enjoyable.

I do believe that Ivan can do almost anything and that nearly any activity presents some sort of learning opportunity. The only way Ivan will learn about the world is through interacting with it. Of course, Ivan may not be interested in art at all - he may be more of an action kind of guy, and that's fine, too. We won't discourage him from running or riding a bike any more than we would discourage him from playing with paints and crayons!

Remember that your child is a child first. Don't think of your child as a blind or handicapped child. Their disability is an integral part of who they are but does not define who they are as a person. Some kids like to draw and others don't; some kids like to run and others don't. Let your child explore the world in their own unique way, encourage this exploration, but don't push them into activities just because it will make you feel better about their disability!

Thank you so much for your articles, I really enjoy reading them and they make me feel a lot more optimistic about my son's vision impairments. They make me realize that, you know what I'm not the only one going through this, and I know I can make it through. There were so many things that I always thought, he can't do it, but now I see he can do whatever he wants to do, I just have to let him try. I hope you keep updating, so I can learn more, again thank you so much for your insight and knowledge. Jenny

Thank you for the great advice. I am a teacher aide at the River Performing and Visual Arts Center for children from 2-19 with special needs. I work with the toddlers, and I find it difficult to describe colors, or to entertain them when it comes to the small art projects. Do you have any other suggestions in how to help them have fun when it comes to art? OR describing their surroundings?

Thank You

My son, Ivan, actually loves art projects. It took us a while to get to this point because he used to have quite a bit of tactile defensiveness and hated touching anything sticky, soft, mushy, etc. He liked hard plastic or wood toys and that was about it. After working with him to desensitize him to other textures, we started playing with a lot of art projects.

You can read about how we helped him get over his sensitivities here: http://www.wonderbaby.org/articles/make-your-own-sticky-box

And more about sensory art here: http://www.wonderbaby.org/articles/sensory-art

I've also posted individual art projects here: http://www.wonderbaby.org/articles?topic=17

You also say you're having trouble describing colors. Have you seen this really neat book: http://www.amazon.com/gp/product/0888998732/ref=as_li_ss_tl?ie=UTF8&tag=...

It's called the Black Book of Colors and each page describes colors in interesting non-visual ways, like "yellow tastes like mustard, but is as soft as a baby chick's feathers." Each page also has tactile drawings that you can feel. It's very cool.

Thank you so much! My daughter is 17 months old. I have had only a few months to cope with my own "feeling of loss" for her vision, and it helps so much to know that I am not alone in how I feel. I cryed for a long time. Kept thinking, "but she will never see pink, or a flower, or so many of the beautiful things this world has to "see". My daughter is my miracle. She was born 3 months premature and had to overcome so many obsticles and challenges in her little life. Then I found out that after corrective retinopathy surgery, that she actually was born with congenitive disease called septo optic dysplasyia. Basicly her optic neverves never connected to her brain.
This site has given me insperation, and I thank you for that. Misty and I have a long way to go, but we are going to have a happy, wonderful life.

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