Home › Forums › Special Topics › Special Topics › update on kaden's dev ped assessment
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May 17, 2008 at 7:54 am #51537AnonymousInactive
Hi!
Another long day yesterday! Finally we are getting somewhere!After the dev. ped. spent 2 hrs with Kaden, she seems to know what is going on and it makes sense!Kaden has mild neuromotor abnormality that directly affects his eating and speech. He also has dyspagia (swallowing difficulty) and mild hypotonia that also affects his jaw/facial muscles also making it difficult for him to pronouce words correctly and his eating.It’s really funny b/c I had his speech checked a couple of months ago through the state and they said it was fine, but their test is saying 1 word at a time and having the child repeat it back. Kaden can say 1 word just fine and pronounce it correctly, giving him the normal to above normal speech. But if you ask Kaden to say a sentence (or if he is trying to tell you what he wants) the neuromotor abnormality that he has makes it very difficult for him and he has VERY poor articulation of speech. He knows what he wants to say but his mouth cannot get it out correctly. this is why he is so hard to understand and gives up after a few tries of saying it. This causes tantruming which is the only real behavioral concern we had. She said this abnormality affects being able to get the mouth to work together to chew and swallow. This is why he limits himself to things that are really easy for him to eat and why he is petrified to eat anything new or of any kind of “texture”.They referred him to their speech therapy dept and to their behavioral psychology dept. so they can start working with him on his behaviors toward food. She said he is very intelligent and well-rounded and some of the things he has are hard to indentify bc they are mild. She said it was good I was persistent to our pedi that there was a problem. 🙂I will keep you posted on his therapy and how he does.jilly78 2008-05-17 07:56:50 May 17, 2008 at 8:32 am #51538AnonymousInactiveWow Jill!! How awesome to have answers finally!! I am so excited for your family to continue this journey and start to see some real results. Congrats on a great visit!!!
May 17, 2008 at 1:49 pm #51540AnonymousInactiveI am glad that the dev ped was able to figure out what was going on and I hope that the therapy helps alot
May 17, 2008 at 9:09 pm #51541AnonymousInactiveThat is wonderful news. I am so glad you are starting to get some answers. Keep us posted. I am anxious to hear how he progresses.
May 17, 2008 at 10:25 pm #51542AnonymousInactiveYaaaaaay!!! Glad to hear the great news!!
May 18, 2008 at 8:36 am #51544AnonymousInactiveThat’s great! Hailey also has/had the same issue. We’ve heard that the eating and speech are often related… if there are eating problems, sometimes the jaw/face muscles aren’t well co-ordinated or weak and you see speech and feeding issues. I guess it’s a chicken and egg thing. I’m glad that you have answers now and can get help. He’ll probably do really well with treatment.
May 19, 2008 at 2:16 pm #51575AnonymousInactiveYayy!!! I’m so happy to hear that things are heading in the right direction! I’m still to hear back from the Developmental Ped to get Tay in for an appointment! But you truly have given me extra hope and encouragement as well as many other moms on this forum! Thank you!
May 20, 2008 at 8:27 pm #51616AnonymousInactiveThat’s great news, Jill.. and what a relief to finally get some real answers and direction and plan for the future!!
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