Would
you ever dream of allowing your son or daughter to receive an education that is
less adequate then his or her peers? Would you deny your child something that
would allow them to be successful now or as adults? The answers to these
questions are obvious to anyone, but all too often it happens to children who
have a disability without their parents ever having any intentions of letting
it take place.
Often
times when parents learn of a child’s disability, especially in the case of
mental impairments that don’t present themselves until later into adolescence,
they are warned to “be realistic” when it comes to the child’s abilities and
future potential. This precept is, however, very flawed. If you as a parent
don’t have big dreams for your child, who will? Children thrive on the
encouragement and support of their parents, so you are in a prime position to
influence your child to be the very best and to succeed. If you have low
expectations for your child, that is probably the level of success that they will
reach.
If we
as parents of children with disabilities truly want our kids to succeed, we
must not only dream bigger, we must also fight harder. If we are told to “be
realistic” then let’s do just that. The world of jobs and employment is a
competitive one. A person with a disability faces an extra challenge of beating
out the competition despite a disability. They must prove that they are better,
smarter, more qualified, than all the other applicants. If we want our kids to
grow up and be successful in the job market, we must not only make them aware
of this fact, but prepare them for it. We must provide them every opportunity
to succeed and push them to do their best even if they have an impairment. We
owe no less to any of our children, disability or not.
The
article that I drew my inspiration from, written by Kathie Snow and also entitled
“What We Owe Our Children” has some great advice on creating high expectations
for our children so that they will one day have high expectations of
themselves.
She says, “. . .let’s be really
realistic about what we, as responsible adults—parents, teachers,
therapists, and others—owe children with disabilities:
·
We owe them an unwavering commitment to have
high expectations for them and to support their dreams, so they can dream big
dreams for themselves.
·
We owe them more than an “appropriate” education
that’s as good as, or better than, the education of students without
disabilities, because they have a harder row to hoe, now and in the future.
·
We owe them an age-appropriate, inclusive
education, as well as participation in inclusive community activities, so that
they can benefit from the ordinary and precious childhood opportunities to
learn reading, writing, and arithmetic; to know how to get along in the real world;
to make friends; and to acquire many other skills that can only be learning in
real world, inclusive environments . If the current public school can’t full
this requirement, parents should explore other public schools , private
schools, or homeschooling.
·
We owe them whatever assistive technology
devices, supports, and modifications they need to enable them to be successful
now, and in the future, at home, school, and other inclusive environments.
·
We owe them every opportunity to experience all
the ups and downs and privileges and responsibilities of a “normal” life: to
try and fail and learn from mistakes, to experience the dignity of risk, to
receive an allowance and blow it on junk, to do chores at home, or other
ordinary childhood experiences.
·
Finally, we owe them our solemn promise that we
will protect them from those who would cause harm through low expectations,
sub-standard education, segregated environments, and/or other malignant
influences.”
This article
provides some insight into raising a child with a disability, and has helped me
to better understand the importance of not letting my son’s disability be a
“crutch” or excuse for him to get by in life, but instead to encourage him to
be great. I hope you enjoyed it and that it has helped you as well. This
article and many more pertaining to the topic of disability can be found at www.disabilityisnatural.com.
Hello Ms. Buchanan. I just saw your video of your sweet son today while looking over yahoo news. You are a brave young woman and your son is a great treasure. I even played it again to have my 6 year old son watch with me to help him understand that we are so much more than what we look like. My own daughter has cerebral palsy and is now 11 years old. I'm sure Christian will grow in acceptance as my Buggy has with her "palsy problems" as she calls them. You've made a great impression on the world. And hearts and prayers now join you in loving that sweet little boy. Blessings and love. Eurydice
ReplyDelete