Sunday, August 23, 2009

5 Little Monkeys Jumping on a Bed


Cole is now 2 1/2 years old and he still can not talk.

I love this video of him playing the “5 Little Monkey’s Jumping on a Bed” game on the Dynavox. You can see he is so excited and he wants to interact with it. He is squealing in delight.

As you may know, if you have read previous posts, we have been teaching Cole ASL as taught on the Signing Time DVD’s.

Cole is very bright and it is obvious he knows what WE are signing to him. There are even some signs that I think he is attempting. But, we don’t want to close any doors and will try ANY means of communication with Cole.

The above video is from when the Dynavox representative came to see if she thought Cole would even be able to use this device. She (Neala) was very kind and patient and feels like Cole is very capable of using a communication device.

With this particular device we have SO many options that would assist Cole. We first tried using the eye scan method. This was very cool. A ‘scanner’ (of sorts) was attached to the bottom of the device and could read both eyes and Cole would be able to scan/choose what he wants with only his eyes.

Well, he would be able to use this IF his abilities made this his only option. This method will not work for Cole as his head is too floppy and he would not be able to hold his head up straight enough to consistently look at the box to choose what he wants.

Another option would be to use a ‘switch’. This looks like the big red ‘Easy’ button that you may have seen in the office supply commercials. Typically this may be located around the head area. Again, I’m not sure this would work for Cole due to lack of head control and….he is a bit claustrophobic about things around his head and would probably completely freak out. Although, we could use the switches for his hand and/or feet. He loves to use his feet so that may be an option for him.

We prefer, and think Cole does too, the last option of Cole simply touching the screen to choose what he is wanting the device to say for him. He does tend to drag his hand and is not completely accurate right now. We think this will improve with practice.

In any case, it is very obvious that Cole is a very smart little boy and he WANTS to use his hands to use this device.

The Dynavox is awesome! It can start out very simple and can grow with him as he learns to talk/form sentences. We can download books (which he totally LOVES) and music (LOVES just as much) and videos, etc.

We are praying that some day his mouth and head and trunk muscles (very low tone) will some day be strong enough that he will be able to talk. If this never happens, then we just want him to be able to communicate his needs and wants and thoughts…in whatever manner that may be.




8 comments:

  1. THIS IS SO WHAT IT'S ABOUT! Whatever it takes for these kids to communicate!

    It is a beautiful thing to read about families like yours who work tirelessly to benefit their child who needs extra help. Keep telling the world...because special kids are here for a reason; they are smart & important too!

    I wish you lots of continued success, Cole! With your family beside you, you can do anything!

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  2. Awesome! You are such a great mom.

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  3. We got ours on Friday too! I am trying to figure the thing out and get going with it. We meet with the ACC coordinator at therapy tomorrow to see if they will get the ball rolling for Jack too. I'm so excited for them both! Smooch my little buddy for me---the more slobbery the better!

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  4. I can't tell you how excited I am about the Dynavox for Cole!!! I truly can't wait to "hear" what he has to say. I really think this is going to open him up. It's SO cool!!!

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  5. I love that you are willing to try anything for him, there is something out there and I can't wait to finally "hear" him! I love and pray for your family!

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  6. That is so cool! You can see his excitement all over his face!

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  7. My son Ethan is eight and we only got our chorea DX a few weeks ago. He uses a DV4 for communication. He started out with the eye gaze pointer, but also really wanted to use his hands. After struggling with activating so many buttons he finally got some key guards, which helped immensely and now he rarely activates a button he did not intend too. This video of your son reminds me so much of my own son at that age!

    Becky

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  8. Cole is such a handsome little guy!! I found your blog by researching RSV. My little Logan will be starting the vaccination soon. Logan has Down Syndrome and is almost 5 months. My other little guy is 18 months and is a great 'lil' big brother;) Looks like Cole has the big bro's to look after him as well...such a sweet face, I just want to give him a huge hug!
    Kireta Nye

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