With the holidays coming, and school soon being done until next year, we won't have another visit from Early On until January. That visit, however, is going to be both nerve-wracking and exciting. We're going to learn about Lyric's IEP (Individual Education Plan).
By agreeing to do Project ImPACT, we will be able to get one on one therapy for Lyric for two hours each week. She will work with Melissa on her speech, and we will have an Occupational Therapist coming to show us what sorts of things we can do to help facilitate a structured "sensory diet" for her. (A sensory diet is a series of structured play activities for Lyric to take part in each day that will help continuously satisfy her sensory needs.) In addition to the therapies, we will be receiving training on how we can supplement and continue all of this learning by ourselves.
The training lasts for 12 weeks, and includes the following topics:
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Set up your home for
success
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Follow your child’s lead
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Imitate your child
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Animation
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Modeling and expanding
language
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Playful obstruction
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Balanced turns
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Communicative temptations
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Prompting and
reinforcement
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Teaching your child
expressive language
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Teaching your child
receptive language
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Teaching your child
social imitation
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Teaching your child play
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Putting it all togetherThe great thing about all of this is that if she doesn't make enough improvements by the time she turns 3, she will qualify for a special preschool that will continue the teachings, at no cost to us.
For the past few weeks we have been going through the process of re-evaluating her skills to get a baseline of where they need to start with the program. It has been somewhat exciting, but it is stressful at the same time. In order to begin the program, we had to "sign her up" for special education. There's a lot of stigma attached to "special ed." in America, so it has been something that is difficult to accept for us as parents. However, as I continually say, this is all for Lyric.
By getting Early Intervention, there is a much better chance that she will be able to make improvements, learn, and grow to the point where none of this will be an issue for her by the time she starts school. It sort of helps "reverse" the effects and take her to the point of being a typical kid. Even if this doesn't happen, we will be able to learn things for ourselves to help ensure that she has a successful future, no matter what. This is why I would encourage anyone who thinks that something may be delayed in their child to contact Early Intervention specialists as soon as possible. Denial isn't going to do anything for your child, and the sooner you call - the sooner your child can receive vital help they may need. Early assistance can help make a world of difference.
I read all your posts, and I love how you write!
ReplyDeleteOn a sort of related side note, I hate the judgment that parents make against each other. I know I have done it and I am ashamed of myself. Strangers and sometimes even loved ones don't know the whole story of your family, so I personally resent smart ass comments people make or the well-meaning but ill-informed ones.
Yes, I'm going to give my kid oreos for breakfast from time to time.
No, I don't spank my kids.
No, I did not successfully breastfeed.
Yes, my kid takes a pacifier.
Yes, sometimes they sleep in my bed.
Suck on it, bitches.
I mean, ya know? lol
I wouldn't worry much about the special ed thing. Kyle was in special ed for several years, ended up leaving it, going to normal classes, and graduating with a 3.9 or something like that.
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