Born-deaf Dunbar second-grader wins UIL prize for storytelling

Miss-Delectable

New Member
Joined
Apr 18, 2004
Messages
17,160
Reaction score
7
Born-deaf Dunbar second-grader wins UIL prize for storytelling - The Lufkin Daily News: Local & State

To win a medal in a University Interscholastic League (UIL) academic competition is viewed as an accomplishment for any second-grader.

For Kade Carr, 7, his fourth-place medal in storytelling is a testament to years of speech and auditory therapy for the boy who was born profoundly deaf.

Carr’s parents, Jason and Beth, discovered their son was deaf at 13 months old. Four months later he received a cochlear implant in his right ear at the Houston Ear Research Foundation. For the next two and a half years, Carr went through intensive and regular auditory verbal therapy to learn how to use the device and rely on his newfound ability to hear.

“Auditory verbal therapy teaches parents how to teach their kids,” Beth Carr said. “There’s a misconception that once the child receives a cochlear implant you’re done. Everything we did every day was a lesson in hearing. Toys became learning tools. It was constant for us.”

The storytelling competition requires students to hear a story that is read to them and then repeat it with as much accuracy and emphasis as possible, Carr’s Dunbar Primary teacher Kathy Goehring said.

The precocious child said he enjoyed competing and likes to tell the stories.
“I like my medal. I was a little nervous, but it was good,” Carr said.
Beth Carr said for her son to accomplish something like this is beyond her wildest dreams.

“He doesn’t see himself as different, but he doesn’t realize how huge this is, either,” Beth Carr said. “This is not just about him, but about what is possible for kids with cochlear implants. Early intervention is key.”

The Carr family moved to Lufkin from Houston two years ago. During their time in Houston, Beth Carr said there were resources all around them.

“When we found out that Kade was deaf, I didn’t know anyone who was deaf,” Beth Carr said, “but we had such a great support system. Had we not been there, I don’t know where Kade would be right now (in his speech abilities). Knowledge is power. I learned everything there was about it. I found that I knew more than some of the ‘experts’ because I did so much research.”

Carr is now a member of the Dunbar Primary Destination Imagination team and in the Tiger Tunes singing group. He is a purple belt in taekwondo and loves to play soccer. He made all As last year.

Goehring said the second-grader is an exceptional student.

“He is a very strong reader and very bright,” Goehring said. “He works hard and is very social. He is reading chapter books and sailing through them.”
Carr relies on his cochlear implants, which send digital pulses to stimulate the auditory nerve, to participate in the world around him. Goehring wears an FM system that directs sound specifically to Carr’s implant.

“It’s important to him, because he is so smart, to do a good job,” Goehring said. “He’s getting something out of it. He learned how to be successful at an early age and that will carry through his life. He’s no different than any of my other kids. He is conscious of listening, and he lets me know if he doesn’t hear something.”

Beth Carr encourages any parent with a deaf child to seek out help and information constantly.

“Fight for what you know is right,” Beth Carr said. “Don’t be afraid to reach for more. What you expect is what they will reach.”
 
When we found out that Kade was deaf, I didn’t know anyone who was deaf,” Beth Carr said,
Doesn't it seem like a lot of parents who chose oral only have NEVER had any real exposure to dhh as kids people?
 
Doesn't it seem like a lot of parents who chose oral only have NEVER had any real exposure to dhh as kids people?

Considering how rare profound childhood deafness is, that is a given.

What is the point of your statement?

If he was not an implantee, the story might be about him winning an ASL storytelling contest.
 
Considering how rare profound childhood deafness is, that is a given.

What is the point of your statement?
Ummm not just talking about profound childhood deafness. I am talking about dhh kids in general. It does seem like a lot of parents who really have NO CLUE about the real lives of honest to god dhh as kids folks, take a gander at the stats and get freaked out (oh noes...deaf school and Sign mean that our kids won't be able to "acheive"
 
Ummm not just talking about profound childhood deafness. I am talking about dhh kids in general. It does seem like a lot of parents who really have NO CLUE about the real lives of honest to god dhh as kids folks, take a gander at the stats and get freaked out (oh noes...deaf school and Sign mean that our kids won't be able to "acheive"

It's just really redundant.

We all know hearing parents don't know much about deafness.

If you want them to know, you need to go out and educate. Harping on it on a deaf forum is an impractical way to spread the word.

I like ASL storytelling too, Jillio. :)
 
It's just really redundant.

We all know hearing parents don't know much about deafness.

If you want them to know, you need to go out and educate. Harping on it on a deaf forum is an impractical way to spread the word.

I like ASL storytelling too, Jillio. :)

Go out where? Readers' section in the newspaper?
 
Go out where? Readers' section in the newspaper?

Go out and find the parents. Volunteer with Early Intervention, go read stories with the kids at the Deaf schools, help at toddler playgroups, join the groups that parents join, help the parents to see that their kids can be successful adults.
 
Go out and find the parents. Volunteer with Early Intervention, go read stories with the kids at the Deaf schools, help at toddler playgroups, join the groups that parents join, help the parents to see that their kids can be successful adults.

Those are actually good suggestions for people young and healthy enough to do it.

Take note, DD. You could have a real impact.
 
Go out and find the parents. Volunteer with Early Intervention, go read stories with the kids at the Deaf schools, help at toddler playgroups, join the groups that parents join, help the parents to see that their kids can be successful adults.

Thank you but I'd rather reach them before they implanted their baby.
 
Ummm not just talking about profound childhood deafness. I am talking about dhh kids in general. It does seem like a lot of parents who really have NO CLUE about the real lives of honest to god dhh as kids folks, take a gander at the stats and get freaked out (oh noes...deaf school and Sign mean that our kids won't be able to "acheive"

Well, in all defense of those parents who "have no clue" -- my parents probably didn't either, but they tried their best. I guess I'm with Botts, I don't understand the point of your post?
 
Well, in all defense of those parents who "have no clue" -- my parents probably didn't either, but they tried their best. I guess I'm with Botts, I don't understand the point of your post?

Thanks! We lived , survived, and have some measure of happiness.
 
I didn't read her to say anything there about implanted babies.

And here I am attempting to help, and still my post is met with animosity. I guess they would rather be angry with me than actually help deaf kids and their families :dunno:
 
Back
Top