Meet our son Jameson.
He's not scary. He's a little boy.
I'm Alice Ann Meyer.
We’ve had some encounters recently that have inspired me to write
this post.
This is something I hope everyone can read.
This is
a message that doesn’t just pertain to Jameson, but to all children who
are made fun of and singled out for their differences and I'm pretty
sure their parents feel the same way I do.
I want to begin by saying that I don’t hold anything against these
children,
or their parents.
I understand that it can be extremely
awkward when your child is the one making fun or being mean to another
child. But, the next time this happens I hope these parents do more.
Because although I cannot take offense,
I would be lying if I said it
didn’t hurt. It does.
It hurts to see my child be made fun of,
knowing
that this will be a big part of his world
for the rest of his life.
By now you might be wondering what happened to prompt these words.
Jameson's Journey. The Blog...
Showing posts with label syndromic craniosynostosis. Show all posts
Showing posts with label syndromic craniosynostosis. Show all posts
Wednesday, October 15, 2014
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