They Hear You

They Hear You

Let me tell you a story about a common misconception: when someone doesn’t respond, they haven’t heard you.

Especially when that someone is autistic.

“Krishna, blue coloured ball!” CLAP!

The ball was bright, shiny blue. It bounced and rolled in front of Krishna, but he resolutely ignored it.

Krishna was about four. It was his first speech therapy session.

The therapist was trying hard to get his attention. He scattered toys. He sang songs. He blew bubbles. The ball was his brahmastram.

Alas, that too failed.

Despite the resounding clap after each attempt, Krishna refused to even look at him.

“Why are you clapping?” I asked.

“Krishna must look at me. The loud noise will attract his attention.”

And he clapped again.

And again.

And again.

No use.

“Is he hearing impaired?” he asked.

“Not at all,” I replied.

This was seven years ago.

It is a different story that Krishna hasn’t uttered a single word in all these years. Nor has he been able to consistently express what he wants through other means.

However, in these years—did he listen, observe, learn something?

Anything?

You tell me after reading this.

A couple of days ago, my husband and I were driving Krishna home from therapy, talking about something mundane. Home repairs, I think.

And quite arbitrarily, I said, “Give Krishna a thousand kisses.”

The same deadpan tone I used while discussing the blocked drain.

“Ha! Ha! Ha!”

Krishna’s immediate glee startled both of us.

I hadn’t expected any reaction. He was curled up in the backseat, hiding under his comforter, as usual.

Back home, he dashed upstairs to his room, to curl up under his comforter there.

I was still downstairs, telling my mother, “You know what happened today! We were talking about something and in between, I randomly said give Krishna a thousand kisses—”

“Ha! Ha! Ha!”

The little eavesdropper startled all of us again.

Hearing impaired?

Hardly.

Once again, I had proof that Krishna’s receptive communication is intact.

Both times, I was speaking in normal, complete sentences—not simplified instructions.

And Krishna does not laugh merely on hearing his name, or when I babble endearments at him.

So, dear parents and caregivers, your child may be absorbing and understanding far more than they can express or demonstrate.

Please be mindful of what you say—and how you say it—in their presence.

Be careful when expressing your disappointments.

Be mindful when discussing them with doctors, therapists, or teachers.

Sometimes, it is best to keep them engaged elsewhere during such conversations, because you may not realise how deeply they are impacted.

And if you are stuck in a blue-coloured-ball-CLAP situation:

First, the child needs time to connect with the therapist or teacher.

Second, the “what’s in it for me” for any task or activity must be made very clear—especially for autistic children.

If you manage both of these, watch the magic happen.

Share this post:

Recent Posts

Look Beyond the Label

I am an author—an award winning author of fiction and this is the identity that I own with pride. Incidentally, the process of getting here involved quashing a few widely held myths about non-speaking autism and this is something that I have learned to take in my stride. It is also something that made me think about the ways in

Share this post:
Read More »

To Be Seen and Heard

The Invisible Weight of Autism Caregiving About four or five years ago, I was on the phone with Krishna’s psychiatrist. I remember I was walking around the garden while I spoke to her because the house was too noisy to have the conversation inside. We were talking about Krishna, of course. I don’t remember exactly what we were discussing that

Share this post:
Read More »

Am I Doing Enough for My Autistic Child?

When “enough” becomes an impossible question—and how to ask what is needed now Am I doing enough? It is such a familiar question in autism parenting that we can almost skip past the word doing and land directly on more. More therapy, more teaching, more research, more doctors, more effort, more money, more patience, more advocacy. Perhaps more sacrifice. But

Share this post:
Read More »

Autism and Medicines: What Every Parent Should Know

“Will my child need medicines?”“What can treat autism?” These are among the first questions many parents ask after their child is diagnosed with Autism Spectrum Disorder (ASD). It is a natural concern. Parents want to do everything possible to help their child, and medicines often seem like an obvious solution. Unfortunately, there is no medicine that cures autism. More importantly,

Share this post:
Read More »

What Happens After Us? (Part 2)

Where Do I Begin? How to plan for your child’s future—one thoughtful decision at a time In my previous article, I shared how Ravi and I came to realise that providing for Shravan’s future would require building a dedicated corpus to support him throughout his lifetime. The realisation was overwhelming. And then came the question every parent in our situation

Share this post:
Read More »

Send Us A Message