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The Wonderful World of Autism

Neuro Developmental Pediatricians, special education, therapy sessions, Persons with Disabilities

These are some of the words I first heard when I learned that I have two kids with autism.Sidney and Red were born full term.I never had problems with both when they were born.Both were
breastfed. They fed,wailed and laughed like any other babies. No problems  with psychomotor abilities
either. They are not picky eaters. They love pasta, fruits and veggies especially Sidney who enjoys
munching carrots and potatoes. They look normal, even good looking as what most people have told
me. It seemed nothing can be wrong until they became toddlers.

When Sidney turned 2 years old,  her speech was delayed. Though she was able to catch up just like the other kids, it seemed  something was not right. Her words were advanced for her age and she  learned to  read and speak  fluently in English even before she went to school.  She also loves to read and tinker with computers, that her ability to absorb words, places and phrases including online games are  faster compared to kids  of her age.

SaraB-autism-children

With Red it was different. His vocabulary was  limited, until now though that had improved because he goes to a special school. His music is his language. He hums, sings like a jazz singer, and never off key. Before,  he does this when he is agitated or nervous like when we visited  his pediatrician or had his head stitched due to a playing accident. Now he sings for no reason at all. While at play, on his way to school or when he wants you to follow him sing with his new learned tune.

Odd looks. Cold stares. Annoyed glares. Angry neighbors and sometimes misplaced sympathy. These
are the reactions we  get when I take them to the mall or for a short stroll even before I ‘ve learned about
their disability. Perhaps one can not find fault in that. Autism, to some, maybe a less interesting subject
until one gets hit with it. One may take the blow hard, others may go into denial, thinking it may just be
a virus, a disease that got one infected and can be cured by a shot.

We have gotten used to it. We have grown accustomed to such questions like “Where did it come from?””Why you let it happened twice?” worst “what have you been doing when you were pregnant?” thinking maybe  that knowing the answers can make a difference.

There must be a reason to all of these that most of us may not be capable of understanding and that there will always be questions. Lots of it. But if one continue living this life with such questions, one may not live enough longer to that day when one finds the answers.

Doors, windows opened. Opportunities knocked. Interviews. Stories. Insights shared. Learning to
look at the world differently,  enjoying the simple things in life, seizing those moments. Like Sidney’s
saying “I love you,” out of nowhere and Red’s constant act of wiping your tears, uncontrollably shed.
Such are these milestones, making you smile and think things may not be that bad after all and eventually will turn better, if you choose to look at it that way.

I have come to realize that there was so much that I have gained when I accepted them as they are and learned to live my life day by day. Respect,  admiration, understanding even from total strangers, now turned into friends. Meeting parents and relatives who share the same struggles like I do. Teachers, gifted beings who take care of my kids when they are in school, giving them the same tenderness and caring especially at times  when they need it. Becoming a member of an advocacy which continuously look for ways to make this world a more forgiving place,  knowing that  now,  I am no longer alone.

I hope that one day, more people would stop, listen and care to know more,  this wonderful world of Autism.

About Sarah Mallari Bucu

Sarah Mallari Bucu

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