parents know their children best

A year and a half ago, my husband and I sat with a group of educational “professionals,” discussing the downward spiral of our eight year old son. A child with disabilities, he began an early intervention program when he was two years old. Now, at grade two, he was halfway through his sixth year of school, and for the first time, he was absolutely hating it. His reading and spelling had regressed, his mathematics skills were failing, and his focus and attention was non-existent.

“He has always been a happy, generous boy,” we said, “who tries to please, and who loves being a part of the social network around him. How could this change so radically within a few months? Now he comes home in tears. He doesn’t want to go to school, insisting, ‘Mom, I’m not smart! I can’t do this work! My brain is broken!’” As the meeting progressed, things started becoming clear.

“It is actually a good thing that your son is seeing this,” said the school psychologist. “The sooner he realizes that he is not going to succeed like his peers, or be as smart, then he can accept and live within his limitations.”

To say we were in shock would be an understatement. All our other children have been taught to reach for the stars, to dream, to figure out ways to overcome their obstacles. I have never heard them told to simply compare themselves to their peers and accept their limitations. Do children with disabilities not deserve the same encouragement?

Unfortunately, the individuals around the table were unable to move beyond their perception of our son’s limitations. As a result, two weeks later we decided to move him to a new school. Today he is reading at grade level, has seen fantastic improvement in independence, focus, and is on a far better academic and social track. It’s been a full year and he loves his school.

Every family wants the best for their children. If you are the parent of a child with  disabilities, you are no different. You want your child to succeed within the parameters of their skills and talents, and you endeavour to secure the resources for them to do so. But no matter how well you equip and challenge your child to succeed and to overcome the impossible societal images before them, someone will try to thwart or undermine your authority. You will have to advocate on your  child’s behalf. And that is no easy road.

You will face someone with power who underestimates or overestimates your child’s potential, and you must, for your child’s sake, be wise, strong, even angry, to get the support they need. Children with disabilities need to be both challenged and assisted while they are young, to gain the personal tools to achieve and reach their potential.

No one can better advocate for a child with disabilities than the child’s parents. No one knows them like you do. Sometimes, though when a parent speaks up they are viewed with suspicion as if they are trying to scam the system. They are told that they need to “settle” for what can come to them, and they should not get their hopes up. Balderdash! People may say they are your advocate, but if they are also handing out the funding, they’re just gatekeepers. Gatekeepers invariably shut people out who need to assistance.

If you know a parent of a child with disabilities, let them know you admire their tenacity. They are heroes, and their children, as with all, are well worth fighting for.

St. Albert Gazette | ‘Dec 16, 2009, 2010 06:00 am | Dee-Ann Schwanke

(See more of Dee-Ann Schwanke’s thoughts at .)


4 thoughts on “parents know their children best

  1. Our 2 year old son was just diagnosed with Autism and the doctor after giving us this diagnosis proceeded to tell us that our son will never be “popular” and never have more than a couple of friends. She essentially had already given up on our son and was trying to convince us to accept that same. This is the person that we are supposed to trust to help our son become the best person that he can be…that scared me to death. So thank you for your article and reminding me I am not alone and that we as his parents are the ones that need to believe in him and help him achieve his kind of greatness:)

  2. Nicole,

    The doctor was wrong. Yes, even highly educated people can be wrong. And you are so right when you say “this is the person that we are supposed to trust to help our son become the best person that he can be.”
    We put our faith into the professionals, while doubting ourselves so often!
    No one knows what sort of social skills your son will learn, because they will grow from his own personal skills, tenacity, resources available to him and the support group around him. You’ll find there will be experts that know about education, psychology, gross motor, fine motor, social, speech, everything, but no one will be an expert on your son but you.
    You will glean your own Phd over the years, and you will need to trust it.
    Well done on a good start … at recognizing the dangers of accepting a “professional’s” words without question. You will grow to love some of the people who work with your son because they’ll “get it.” Others, you will need to train. Still others, you’ll pressure or even reject.
    It doesn’t matter if you’re always right. It doesn’t matter if you know any more or less than they.
    You’re the mama bear, and they would be wise to not get between you and the boy.

  3. It is amazing that there are parents out there that will fight, challenge and persevere for their children. I am a result of 2 of those parents and believe me I would not be the wife, mother, and have a successful career if it were not for them. Thank you to all those parents who know their children enough to know they are meant for more in this world than just a diagnosis. You parents are the super hero’s in this world and to
    your children.

  4. Well said, Jodi.
    You are the perfect example of someone who’s parents’ commitment changed their child’s life.
    You are an inspiration to me.
    Thank you!!!

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