An open letter to my friends;
Parents ~ it starts with us.
Ethan has had an increasingly difficult couple of weeks at
school this year. Yes, I know the year just started, but when you have a child
who doesn’t want to attend class, it seems infinitely longer. For the last few weeks (and even prior to
school starting) we have had several painful conversations with Ethan where he
has said that the children at school “make fun of him, are mean to him, tell
him he has a tiny head, laugh at him, and hurt his feelings.” It is absolutely heartbreaking dialogue to
have with your child.
Before I had Ethan I only knew a handful of people with
disabilities. I wasn’t exposed to it
growing up. Very much like Sherwood, I grew up in a community, which albeit
wonderful, was not very diverse. We are
afraid of what we don’t understand. When
we received Ethan’s diagnosis of microcephaly I was afraid. When we took him to
his medical appointments and under the section reason for visit it listed “mental retardation” I was afraid. But knowledge is power.
We have all been teased or ridiculed at some point in our
lives. Maybe because you were poor and didn’t have a lot of clothes (a painful memory for me,) perhaps you had glasses, or braces, or freckles. It hurt and it cut deep. Multiply that times one hundred when it comes
to your own child. Worse than having a plethora of medical appointments where
your child is constantly poked and prodded, worse than therapy several times a
week, worse than not knowing your child’s future. As
parents, you know that seeing your child upset and not being able to do
anything is pure agony. However, in this
case, we can do something.
Talk to you kids. It begins with us. Tell your children it is
okay to be different. Discuss inclusion and empathy with them. Encourage them to have a diverse group of
friends, to be independent thinkers, to stand up for those who can’t stand up
for themselves. Lead by example. Start with a simple conversation. Start
young. And repeat.
Your child could be the one to make a difference in another
child’s outlook on school or even on life.
Have a question… ask! Need help starting the conversation? I will assist
you. Let’s begin to spread the knowledge to our children now!
Thank you, on behalf of Ethan, and all the other children that I know feel the same.

2 comments:
Beautifully put.
From Another Mother with a Child with Microcephaly (among other things)
Great post Lindsey! I have a few close relatives with disabilities so it's always been a soft spot for me. From the time my girl was able to understand made it a point to teach her that being different isn't a bad thing, and that she needs to stand up for anyone being picked on. I'm so very sorry he has to go through this at school. Hopefully this post will touch the hearts of many parents who hadn't thought about teaching their children these lessons. <3
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