I met with Nathan's occupational therapist yesterday afternoon about The Listening Program. Here's how it works. It is 10 cds that the patient (child or adult) listens to 1 time a day for 15 or 30 minutes during the 5 week days. Weekends are 'off.' Each cd contains... I think 4 segments. With the OT group we're working with, it generally takes 20 weeks to go through the cds from 1 to 10. Then, they go back through the cds from 10 to 1. So, overall, the program takes 40 weeks the first time through.
The cds contain 3 different 'zones' of acoustically altered music. The first zone is lower frequency sounds intended to target sensory integration overall. The music is special - I can't give enough info about it - check out The Tomatis Method for info on it. The second zone contains only music in the frequencies of conversation. So, very low and very high frequencies have been removed. This section of the cd's is intended to help with language. The third zone contains only high frequencies. This set is intended to help with energy.
I called our developmental pediatrician about this program before meeting with the OT. He has seen both great and non-existent results with the program. He said that he would absolutely go for it if we'd seen Nathan react the way that he did on Monday.
Okay, here is my very nominally informed theory (very dangerous ground). There are so many ways to have sensory integration issues - audio, visual, tactile, vestibular (movement and balance), propreceptive (sense of where you are in space and where your limbs are in relation to your body), smell, taste and more. Because there are so many different areas of sensory input and senses to have integration issues with, it seems to follow in my nominally informed thinking that the same solution wouldn't work for every sensory system. So, the same thing might work great for one person and have no effect on another person. The brain is a very complicated organ! And, the brain is where all this integration of sensory input occurs.
So, if Nathan responded well (I still haven't seen it - we couldn't get the headphones on him yesterday afternoon - uuuurrrrgh!) to the auditory therapy that The Listening Program is, then maybe his biggest issue at the moment is auditory. Who knows. We're certainly willing to try it.
I'm painfully aware of the fact that I'm constantly searching for a silver bullet and that there may not be one. I can't stop myself. It's like my brain knows it isn't helpful, and my heart just can't seem to stop.
Okay - very quickly (because I totally forgot that I have sensory integration learning to share - I'll do that next time), the meeting with DeKalb County Public Schools for Nathan's evaluation was interesting. They were extremely accommodating to us - I suppose because Nathan is so young. The 'test' was LONG. 2 hours. Ridiculously long for a 2-3 year old. We had two people testing Nathan at the same time - a developmental specialist and a speech/language pathologist. I think they wore him out. We were sitting at the end of the table with the developmental tester on our left and the speech/language tester on our right - they were sitting around the corners of the table from us. So, we everyone was quite close. The developmental tester would be doing something with Nathan, and the speech/language lady would get her stuff set up - right in his line of vision and distract him. I don't know, maybe that is part of the test, but it didn't seem like it.
Nathan behaved fabulously. He is such a great kid. We went an hour past his snack time, and, thank the heavenly father above, he did not melt down. WOW.
At the end of the test, I asked them what their initial thoughts were. And, of course, they didn't tell me a thing - really, because they can't. But, it was still hard to hear!
What they did tell me was that Nathan's eligibility for special education wouldn't be up for negotiation - that he had to score some number (can't remember - 1 or 2?) standard deviations below the mean score in at least two areas in order for him to be eligible. They also told me that if he's eligible, they will make a recommendation about how they think they can best serve Nathan, but parents have a BIG say in that. So, while I can't beg for him to be eligible if he isn't, I can say exactly how I want it to go if he is. I think I can live with that -- well, I might have a different attitude if he isn't eligible!
Deep Pressure and Joint Compression update - we have stopped doing the 'brushing' or deep pressure program with Nathan for now. He was taking longer and longer to fall asleep at night. I think it was just a LOT of input for him. I can say that we've noticed him being more interactive and responding more to our questions and requests of him. I don't know for sure if it has been that program that has caused these changes - we have a new nanny who talks to Nathan a LOT more in addition to adding in the DP and JC program (too much typing!). I talked to the OT about stopping. She was fine with it because we'd been doing it for 2 weeks (the minimum that the developers of the program say it should be used). I told her I'm not against trying again, but I really think that Nathan needs a break.
Okay - I can't wait to share with you what I learned from Christy Kennedy about Sensory Integration yesterday. But, it's too much to write now; this is too long already, and it's getting late...
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