A little later we found that his speech was not developing into
sentences. The words were there but no progress. This sounded the alarm bells for
us. Apart from this, well wishers, neighbors, and relations started asking why he
wasn’t talking, And so started our visits to the doctors! When they said, “Nothing
to worry…it will come. It looks like a delay,” we came home happy! All this was when my son was two and
half years old. At three years of age it was time for school. The school wanted
us to go for another review of tests—this was also was to our relief. At school
we found he could do the writing and mathematics but verbally he was way, way
behind his peers. So he repeated the class.
We started the next round of assessments as the school was very particular to
get him tested again. NOW we found various doctors giving him a wide range of diagnosis—from
mentally retarded to hearing loss, with strong advise to put him in special
schools.
Way back in the late seventies and early eighties there weren’t
many special schools and most of those were far below in the matters of hygiene.
This made me advocate for regular schools. At that time I happened to meet a Reverend
Sister who ran a school for children who are deaf and/or hard of hearing. She said,
“It looks like he has Aphasia. That is a language problem…an inability for the
brain to learn language.”
In the meantime my son started in a new school and he did extremely well there. Everything was fine till seventh standard. The school was very nice to him—they encouraged him in sports level, drama, etc and he was happy with friends. At this stage he had problem learning new words and remembering them. We started giving him pictorial clues and he was able to recall well. We also got language exemption and and things started looking fine.
Even though his speech was not great he was able to manage
to travel alone by bus, get his things done independently, etc. He had speech
therapy for a short period. In my opinion it was a waste as they were interested
only in the money and not his language
development.
With the language exemption in our bag that year, I thought we'd
won the battle. I was happy that he didn’t have to struggle to learn a second
language. My hope came crashing down when we went to get the exemption from the
department of education. Well, only when
we applied for it did we come to know that it is time consuming and money had
to be given at all stages to get the exemption. Not only that, we had to get the exmption
every time he appeared for a public exam! In our country people try to make hay
even out of someone else’s misery. I guess that is a different story for a different time.
In this manner, my son finished school and then got into the university for his graduation course. He took visual communication and got through with flying colours. The three year course was like a roller coaster ride for him as well as for me. There were a lot of hiccups along the way like running around for the exemption, being ridiculed by his peers, not finding a good friend, plus the pressures of college life, etc. The list can go on and on.
We sailed the stormy oceans and one fine day he graduated and got into a job with one of the best companis in
I asked for this narrative even though the writer's son doesn't have any mental health issues...to highlight the fact that any child with a disability can have periods of extreme stress because of how the community responds to his/he need. School officials and teachers should be aware of the needs of the specific disabilities and also the social/emotional needs of all the students. Many children develop coping skills and adapt to their learning needs; but having good friends and supportive peers go a long way in developing positive self image. Parents can look for various resources to supplement intevrention but where do children send most of their awakening hours? At school! Our schools have to address this need deliberately.
Good post... and good blog
ReplyDeleteThank you Ketan:)
ReplyDelete