3/21 -World Down Syndrome Day.
Today, I am celebrating with my son who reads, writes, is never sick, and happily works a grueling program with me everyday while typical peers achieve the same thing without effort - and in the process can do many things “typical” 5 year olds can not. Our goal is not fitting in with peers, but rather to emerge as a leader. Lucas will join his peers when our work is through, he will sit for entrance exams to private high schools and he will go to college.
Today is not about bringing awareness to my son and finding a way for
him to fit in the world. It definitely isn't about the cute little
"special" category into which prejudiced people like to fit my son. It
isn’t about “tolerance” because society has no right to arrogantly
decide they have the choice to “tolerate” my son - or any member of the
human race - as if the random chromosomal alignment that shaped my son
couldn't just as easily been you or your child.
This day isn’t about my child, it is about yours. Will your children accept Lucas
as a peer or look at him as less? Will your children accept his
accomplishments as valid, or dismiss them as a fluke? Will your children simply see his almond shaped eyes as part of him like skin color or
orientation - or will they use it as a means of segregating him. How
will you feel when Lucas sits next to your child at the induction
ceremony to National Honor Society? Or asks your daughter to the prom?
It isn’t about “inclusion,” because arrogant school systems who fail children like my son have convinced parents it is their child who can not learn, instead of a system that can not teach. It isn't about specialists ingrained in the past who call my son "high functioning" when he can do things his typical peers can't. I have never asked the world to see my son as special, or to make special considerations for him, nor will I ever. He is a member of the human race with strengths and weaknesses - the same as your child.
This day is about equality, respect, fairness, and humanity.
You have my word that is how Lucas is being raised to treat your child.
A place where achievement, expectations and dreams for babies and children with Down Syndrome thrive! This blog was started by an Occupational Therapist and mother of a 3 year old boy with Down Syndrome (hereafter referred to as T21), who refused to believe the stereotypes and set out to form her own action plan. Armed with a Master's degree in Occupational therapy she set out with an insatiable desire to redefine the reality of what it meant to receive a diagnosis of T21 today.
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