Rarely do children born with Down syndrome receive the warm welcome
they deserve. Their births are often accompanied by grief, denial
and disappointment. As new parents learn more about life with Down
syndrome and shed their own misconceptions, they must still face the
outdated stereotypes and ignorance of family, friends and society
at large.
Society’s attitudes about Down syndrome support a subtle barrier
that becomes clearer as we grow with our five year old son Nick.
While there may be many ways to describe it, much of it distills
to something Nick asks constantly as his older brother and sister
leave him behind for soccer practice, to go play with friends, or
to do those things that older kids do. “How ‘bout me?”
We fear that Nick’s presently innocuous question will cut deeper
as the years pass, for people with developmental disabilities too
often are left wondering the same thing as they try to participate
in our community in ways we all take for granted. How ‘bout me?
More and more doors are opening for the developmentally disabled.
But simply opening the doors is not enough: weaving them into our
churches, our schools, our community requires more than a willing
attitude. It requires effort. It requires work. It requires active
support.
We know that you here tonight are willing to embrace people with
Down syndrome, but how do we answer those who ask why the community
should take the time, effort and, yes, expense to really include
them. The answer is simple. We should work to include them because
they are worthy human beings that need a little support, because
they are amazing people who, if given a little extra help, will
blossom into joyful, truly capable members of society, because it
will enrich the world.
Thank you for joining us tonight to support those affected by Down
syndrome. With your assistance, we can work to change attitudes
about including the developmentally disabled in our community. Perhaps
one day we will see a time when our children no longer have to ask
“How ‘bout me?” |