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#1
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#2
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![]() Go Kaylee! I don't have any any answers for your questions. I'm sure others will.
__________________ New to CWE? I suggest reading the proactive prescription and epilepsy 101 threads. Also check out this chart of alternative epilepsy treatments and this page on EEG Neurofeedback. More great stuff can be found in the list of the best forum threads. Would you like to help support this forum? |
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#3
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| Does she understand what you say to her? If yes, that is the first step and she will catch up eventually. Have you tried baby sign language with her? I had my eldest daughter ( now 11) who had severe development delay she was diagnosed with epilepsy at 9, but we believe it's been going on for years before that. She communicated with signs until she was 5 1/2 when speech just burst from her. sign language can take away a lot of the frustration. Speech therapy may help also. She was also very delayed with her motor skills and even now she is 3 yrs behind in her english work at school and 5 years behind with her maths, but she is slowly catching up. She started to read 3 letter words when she was 8. She is in a mainstream school with extra support. She is just going up to secondary school in a few weeks. If your daughter can point to a picture in a book when you ask her to i.e. if you say point to the doggy and she does, then she will eventually get there. It just may take a little longer. Have you ever read the poem 'welcome to holland'? If not then PM me and I will send it to you, it's a brilliant poem. |
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#4
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| I totally forgot about using sign language. We did that with our kids and they made up their own signs for things before they were verbal. It was really cool.
__________________ New to CWE? I suggest reading the proactive prescription and epilepsy 101 threads. Also check out this chart of alternative epilepsy treatments and this page on EEG Neurofeedback. More great stuff can be found in the list of the best forum threads. Would you like to help support this forum? |
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#5
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| Rebecca was delayed. We began free speech classes in the local public school at the age of 3. She remained in speech until 5th grade. As a 3 and 4 yr old it was noticable, but as she grew it has not been noticable to any one else. I remember wishing she would begin putting words together. She developed her own sign language, but of course I was the only one that knew what she was saying. Then over time as her chatter was increasing I remember reminding myself that there was a time I wanted to her talk. So occasionally we would play the "quiet game". Surround Kaylee with loving people and try not to speak for her. Sometimes they use us as a crutch. Keep a record of her progress, and I bet you will see that over time, she is making leaps of progress. Just sometimes hard to see in the moment or as compared to others her age. ** I wanted to add something.... find other ways for her to communicate her feelings. Rebecca's was through dance. She excelled at it at a very young age. Art is another great place for them to find a "voice". Music too.
__________________ Robin Neurofeedback - Rebecca's Story Feedback Matters- blog Knowledge is power and knowledge shared is power multiplied. -- Bob Noyce Last edited by RobinN; 08-16-2009 at 11:40 AM. |
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#6
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| Thank you for all your personal stories and tips. Kaylee is in speech therapy, and deep down I know she will catch up. As you all know, it's just hard sometimes. We are going to the neurologist tomorrow, and I am going to see if he suggests anything else we might do. Thank you all again. Leslie G. |
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#7
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I wouldn't suppose that the neurologist would not know of many options in age appropriate learning. Find wonderful people to surround Kaylee. Opportunities where she can excel, and the confidence that she can overcome obstacles. She will be an exceptional child, because she will "know". Hugs to her.
__________________ Robin Neurofeedback - Rebecca's Story Feedback Matters- blog Knowledge is power and knowledge shared is power multiplied. -- Bob Noyce |
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