Today
I visited my little boy. Little? Well, not really. He’s all of 17 years old
now. He’s tall and well built and he needs to shave from time to time.
The problem is – he never got to grow up.
I
watched him run down the corridors when he was in class 8, his laughter
trailing behind him as he dodged his best friend. He had come off the football
field and he was grubby, his face glistening with perspiration, his face alight
with mischief. He looked like he had worked up an appetite, but I
wasn’t in the least worried – if he’d finished his own Tiffin, he’d probably
just nab someone else’s. That’s how it goes – a way of life In St. John’s.
Gradually,
however, one began to notice a change in him. The light seemed to die. Was I
imagining it, or was his gait less steady, his speech ever so slightly blurred?
I prayed I was wrong. But then his mother came in to meet me. It seems Adi was
suffering from the rarest of rare medical dilemmas – his body had ceased to
produce an enzyme.
“Just
one enzyme?” I asked hopefully. “Then it couldn’t be so bad, could it? Surely
there’s a synthetic one available that can be injected as a substitute?”
The
answer, however, left me bereft of words. It seems that there was no substitute
and that this enzyme is responsible for the white and grey matter of the brain
responding to each other and triggering the motor reflexes of the muscles.
Adi
was losing control of his body.
Despairingly
we watched our little boy struggle. His steps slowed, his speech slurred and gradually
he faltered to a brave halt. Adi was now confined to his bed. He could no
longer respond to auditory or any other signals, no matter how bravely he
struggled to do so. The frustration and pain were palpable – the desperate need
to answer - willing his useless limbs to work and the soundless cry of despair
as even his voice failed him and silence filled the vacuum of his life.
Soon
he was confined to a hospital bed, tracheostomy in place. Even his eyes had
ceased to obey him – rolling violently around as his body convulsed with the
effort to remove the accumulated mucous trapped in his windpipe. I watched, my
heart pounding out its own rhythm of fear, as it was suctioned out and his
thrashing subsided for a brief period only to begin again when the slime
collected once more and the whole sad story repeated itself in a terrifying
cycle of hopelessness.
And
then something strange happened.
I
spoke to him, calling his name out loud. They had told me he did not respond to
such signals any more. But I could have sworn he heard. A stillness came upon
him, the rattling cough diminished and a sense of peace seemed to steal across
him. Was I imagining it? I don’t know. But I continued to call out his name,
stroke his face gently and speak to him of everything and nothing. I told him
we loved him and had not forgotten him. I told him his friends often spoke of
him and they missed his cheerful presence in the class. He was never very
talkative, but he had a calm presence that made his peers take notice of him and
I told him how the class missed him. Then I hugged him and left.
Later
that day his mother called to say that Adi had had a peaceful day after a long
time.
I
hadn’t imagined it.
From
then on I tried to visit Adi as often as I could. His class organized visits by
the boys and when the class photographs were taken, Adi’s image was morphed
into it. His friends were unwilling to leave him out. “It won’t be complete
without Adi, ma’am,” they said. I agreed.
His mother wept when they presented it to her.
Adi
lay and listened.
Christmas came around and I dropped by
to say ‘hello’ to my little boy. Our church was praying for him regularly and I
wanted to tell him that. To my surprise, I heard Christmas Carols playing in
the room. His mother told me how Adi had always loved Christmas and had
insisted that a Christmas tree be put up each year. I noticed a tiny Christmas
tree on the ‘fridge. I offered to bring in some friends – we were in the middle
of doing our caroling rounds. Three of us came to sing for him. We sang his
favourite carols and said a quiet prayer for him. Adi quietened down
immediately.
The
medical experts can say what they want. I knew our child could hear us.
The
years have rolled by since then. Adi’s classmates are in Class 12 now. In
between I have gone to see my little boy and watched him grow. The selfless
love with which his mother waits on him, leaves me humbled. Her unfailing
cheerfulness and her belief in the prayers being said for her son, are a lesson
to me in faith, patience and fortitude. She tells me how she has grown as a
person and I have watched fascinated as she has counseled the attendants of
other patients with a calm assurance and wisdom that has made a distinct
difference in their demeanour.
So
today I visited my little boy again. To my shame, it has been almost a year
since I have seen him. I have no excuses to offer. The fault is mine and mine
alone. But what I saw made my heart sing. Gone is the terrifying restlessness. His
eyes don’t seem to roll so violently. He seems to be waiting for something.
Then the door opens and Adi’s father walks in.
He
hugs his son.
And I see Adi smile!
They
say the age of miracles is over. They lie. I know with absolute certainty that
Adi hears me. I also know that someday Adi will walk again.
Because
I believe in prayer. I know there is a God in heaven who listens when we speak
to Him. I also know He answers.
Will
you pray with me?
Beautiful, inspiring and touching ... And yes, I will pray with you and Adi's family ... for Adi
ReplyDeleteThank you. He is such a special child.
DeleteYes I will pray for him..no words to express how each word stirred me..will continue to pray for him ..
ReplyDeleteYes, he is one of our own young ones and how often we have been privileged to see the miracle of prayer restore our children to us. We have seen it happen far too often to doubt that God does answer prayers.
DeleteBeautifully expressed! May God continue to reveal himself to this family. We continue to pray for him.
ReplyDeleteAlmost & about to got tears out after reading this....Could be the way the so far journey is explained....Dont know personally this kid but got attached.He is Fighter and we pray for his well being and good life ahead..Thanks to you Kavita Ji!!!
ReplyDeleteThank you Ravi. Please do hold him in prayer. God's ways are strange and mysterious but I have seen His grace time and again and I know with absolute certainty that He is good.
ReplyDelete