Special Kids Needs Special Parents
From Manila
Standard, July 22, 2000
I.
SUMMARY
Romeo
Conrado, a 10-year old child was diagnosed in 1990 with cerebral palsy
diplegia. According to his mother, Mrs. Ana Libunao she haven’t faced any
difficulties with her pregnancy. The only thing she noticed was the kicking of
her baby and moved nonstop intervals during the pregnancy. And when she gave birth, Romeo came out reed
thin because he is a pre-term baby at seven months. There is quite different in
Romeo according to the nurses. They found out that he clutched for air that’s
why he kicked hard and the umbilical cord was found all tied all over his neck,
causing in insufficient maintenance of air.
When Romeo was an eight month old, they’ve noticed that
he could not carry his head well. He moved it endlessly in a counter clockwise
manner. The pediatrician recommended
them to see a neurologist to better assess Roco’s ailment and the assessment
resulted in having a cerebral palsy diplegia. Roco’s brain suffered from
central and peripheral atrophy resulting in damaged motor skills. At first his
parents had a denial and could not imagine the magnitude of negative feelings
but it took them some time before they are able to move on. Because his parents
don’t have a stable job so his parents struggle to gathered free or cheap
services to render in their son’s condition.
II. REACTION
Cerebral
Palsy is a range of neuromuscular disorders caused by injury to an infant’s
birth sustained during late pregnancy, birth, or any time during the first two
years of life. Cerebral Palsy causes a
wide range of difficulties, from a clumsy walk to an inability to speak,
swallow, caused by faulty messages sent from the brain to the muscles.
In
the case of Romeo Contrado, son of a very loving mother, Ana Libunao who faced
unto this situation. Roco was a pre-term baby at seven months old causing to
brain damaged from central to peripheral atrophy, resulting in damaged motor
skills. In the article mother had a denial stage wherein she asked God for
letting this happened. Living in a
simple way in such both parent don’t have permanent work to sustain the needs
of their child, they are bothered on the future of the child. We all know that
educating the child nowadays with exceptionalities is a very tough thing to do
because of lots of expenses from diagnosing, assessing a child a letting him to
be in school.
As we all know, the population of the Philippines is increasing every
year. It also means that there is an increase of special children with
special needs like those who have cerebral palsy, mental retardation, ADHD
and autism. A lot of teaching techniques have been introduced and are being
used in SPED schools. As we can see, the
education of special children here in the Philippines is really expensive.
Before a child is enrolled, they still need to observe, assess and evaluate him
as each kid has different needs.
The main question is: What if the parents of
the special child in the Philippines do not have enough money to send their
kids to school?
The usual answer: Consult a Public School
Today, we usually hear news reports about the shortage of
books, school supplies, classrooms and the like in public schools. What
more for public SPED classes? (I can imagine a worse scenario.) In countries
like England there are public schools which are supported by the government to
render free services to children with special needs held their free tuition fee.
We know parents who would enroll their kids to normal schools in spite
of the fact that they know that their child has special needs. Ok, you
enrolled him in a reputable school and the administration gladly accepted him.
Do you think he will do just fine? Do you think he can meddle easily with his
classmates?
I am not saying this to make the parents of special children feel bad or
to discourage to enroll their kid in a public SPED school. I’m just trying to
say that this make an appeal to the concerned individuals to also focus on
SPED. The increase of children with special needs is alarmingly growing.
They have the right to educate and a right to live a normal life. Parents do
want the best for their children so work on the program that are best for these
kids and follow them correctly. There may not be any cure available for their
conditions now, but they can possibly improve for the better.
In
case of Roco, his parents can’t afford even the wheelchair to help him move
because his motor skills damaged and the therapy needed by him. In this
situation, the parents should give him the same amount
of both love and discipline you would to any child. Having Cerebral Palsy
doesn't mean they need sympathy and create a stimulating learning environment
in the home. Don't be disheartened with no answer or no repetition from the
child. Keep continue stimulation. She need to be patient and to provide
different clues for the stimulation is needed and enjoy and respect her child's
individuality.
It
is important to take care of one’s health most importantly when pregnant
because their might be complications that will affects child’s condition. Good
sources of professionals are very helpful in sustaining the good health of the
child in the womb. I can’t misjudge the reaction of both parents when they know
the condition of their child because every parent wish a healthy child but then
a special one is given to them by God so they should take it as a gift for
them. Parents should be strong in front of their child so it will give them
hope to dream and continue their lives.