Sleeping, Listening, and My Fourth OT Visit

Note: For posts about previous visits, including my sensory assessment, see the Occupational Therapy category, to the right of this post.

After receiving so many wonderful ideas from all of you about my sleep resistance dilemma, I went to see my OT on Monday. The first thing she had me do was to write out a list of objectives for the therapy. A list! I was so happy.

Objectives

  • To stop resisting sleep by eating and watching TV.
  • To reduce auditory overload. (Auditory overload seems to be the most intense for me, followed very closely by visual and vestibular overload.)
  • To do the grocery shopping one day per week, every week. (My husband does most of the grocery shopping these days.)
  • To deal better with changes to my routine. (I don’t get upset with people anymore when plans change, but I still get very stuck and have difficulty adapting.)
  • To keep up with OT tasks, such as exercise, singing, and drumming.

We began working on the top two issues on the list: sleep resistance and auditory overload.

Sleep Resistance
We talked about my sleep issues from a sensory point of view. My OT feels very strongly that I need to reframe the way I see winding down, ending the day, going to bed, and sleeping. Right now, I resist all of those things. She said that I need to frame all of them as being very positive. Sleep is the time that our bodies regenerate cells. Sleep provides rest for the immune system and for the nervous system. Both systems are key to the health of the body and to the enjoyment of the daytime hours.

We then discussed ways to take care of my sensory needs so that I don’t try to calm myself by watching TV and eating too much. It’s clear to me that what calms my nervous system is a lot of physical, tactile pressure, like the pressure of a weighted blanket or the vibrations of the Thumper. On Passover, I fell asleep under two weighted blankets—30 pounds of pressure. Since I’d like to start going to sleep earlier, my OT suggested that in the evening, when I imagine the best possible place in the world to be, I imagine lying underneath 30 pounds of weighted blankets at 10:15 pm! Talk about reframing. Given that lying under weighted blankets feels a little bit like heaven, I think I can do it.

As we talked about the process of replacing one routine with another, my OT was very adamant that I not completely ditch the old way of doing things until I add something more powerful to it. My tendency is to try to jettison an entire routine before I’ve started on a new one. The results are usually not good. So this time, for example, I will not take away chocolate without giving myself something that works better. In other words, I need to respect that I am in a transition. Transitions are difficult, but I’m willing to put some energy into this one.

I’ve decided to make some changes. Over the past couple of days, I’ve taken a look at my daily list and given more attention to the times for my late afternoon and evening tasks. According to the list, I have different self-care tasks and chores to start by 4 pm, by 6 pm, and by 8 pm. Up to now, I’ve been getting the tasks done, somehow, but I’ve paid virtually no attention to the time at which I get started. For example, sometimes the dishes get done at midnight, even though according to the list, they should get done by around 8 o’clock.

In addition to keeping better track of my present tasks, I added a new task, which is to make myself a very weird but useful concoction of mashed bananas, soy powder, and tahini at 10 pm. I used to eat this little concoction when I was on an elimination diet to weed out food allergies and sensitivities. It always helped me to feel full so that I could fall asleep. So, on Monday night and Tuesday night, I had this lovely dish and also allowed myself a small piece of dark chocolate. On Monday night, I feel asleep at 10:30 pm, woke at 4:20 am, and then meditated myself back to sleep until 6 am, when my alarm went off. On Tuesday night, I fell asleep a bit later, around 11:15 pm, woke up again at 4:20 am (not sure why, except that perhaps the heating system was coming back on), and then fell back to sleep until about 7 am. Not too bad at all. I didn’t watch TV either night.

I can see that this whole transition is going to be a one-day-at-a-time proposition.

Therapeutic Listening
After our conversation about sleep, my OT and I went into the gym and began the Therapeutic Listening program. The goal of the program is to help me filter out sounds in my environment so that they don’t feel like they are all rushing in at one high volume. It involves using a special headset and a series of CDs.

While lying under a heavy weighted blanket, while standing up on a swing and rocking laterally, and while rocking laterally on a peanut-shaped physioball, I listened to part of a CD called Mozart for Modulation. The makers of the Therapeutic Listening program take pieces of music and change them in ways that work the muscles in your ears. The music is supposed to be in the “background” to make your ears reach for some of the sounds, so I heard it at a low volume (from 2-4 on a CD player, without any bass boost), and I could still talk to the OT without needing to speak loudly. I was supposed to listen to the music while not actually concentrating on it (not so easy for an Aspie), so my OT had me swinging and rocking while I talked to her about, well, whatever—my daughter as a baby, what her sleep patterns were like back then, and a lot of other stuff I don’t remember.

Listening, talking, and moving were a lot to do at once, and I felt pretty tired and disoriented by the end of the session. My system really resists that amount of multitasking. But the OT said that the point of the therapy is to ask my brain to attend to several things at once without getting overloaded. I overloaded this time, but the goal is to begin to reduce the overload, so I’m willing to commit to this program and see whether it helps.

I brought home the CD and special headphones. I don’t have a portable CD player, and my OT said it was okay to listen to the CD on my computer, as long as I wasn’t watching the screen. (She said that, under no circumstances, should I listen to the CD while driving or watching anything on a screen. I don’t know what happens exactly, but it doesn’t sound good.) I was supposed to combine movement with listening to the CD, but right now, the only way to move and listen at the same time is to put the computer at the foot of my bike while I’m working out. I really don’t want to do that, because I love the routine of biking and singing my favorite songs. My OT agrees that I shouldn’t interrupt that routine.

So yesterday, after work, I came home, got myself organized, lay down under my weighted blanket, and listened to 20-30 minutes of Mozart for Modulation until I fell asleep! I really enjoyed lying under my weighted blanket in the late afternoon and listening to the CD. It was the first time that resting felt like a good thing, because my mind was occupied with something other than my own constant thinking. Since it feels so nice to me, my OT said that once a day, I should listen to the whole CD while resting, and then listen to it again at some other point, while I’m moving around. Moving around can include walking, eating a meal, knitting, making mobiles, or doing the dishes. The goal is to activate and integrate the visual, auditory, and vestibular systems. The CD is nearly 75 minutes long, so I’ll need to work up to listening to the full CD twice a day.

[Correction: I just heard from my OT, who reads my blog. She said that I only need to listen to the CD for 30 minutes, twice a day, with at least three hours between listening sessions. She said that the beginner CDs are 30 minutes long, and that she had forgotten how much more music was on the one she gave me.]

Of course, I finished off the OT visit with the Thumper, and this time, I could feel the vibrations in my teeth! Very cool.

© 2009 by Rachel Cohen-Rottenberg

8 comments

  1. Quirky Mom says:

    Every time you mention the Thumper I cringe, and this time I want to run away screaming! I am so overly sensitive to vibrations it isn’t funny… the idea of my teeth vibrating. ***shudder***

    BUT I’m glad it’s working for you. ;) I’m interested to follow your sleep progress, but so far so good!

  2. I so badly want to see an OT after having read of your very positive experience. Does insurance help with this at all? If so, do you have to have an official diagnosis for insurance to help out? My therapist back in the states is brilliant, and treats me as someone who has asperger’s, even though it is a self-diagnosis. She agrees that my diagnosis is most likely accurate, but will not give me a diagnosis as she feels someone with more experience in that specialty would be needed (and I greatly appreciate this). Before this point we never felt an official diagnosis was necessary, but if it would help pay for things like this, than it would definitely be worth it!

  3. Rachel says:

    Our health insurance should help pay for the OT, but we’re having a hard time of it. My primary care provider made a request for referral authorization in March, but we haven’t heard yet. Partly, the issue is that my OT is in MA and I’m in VT, so she’s not a network provider. It shouldn’t be an issue, though, because she’s the only one I could find within an hour in any direction who would see an adult for sensory integration issues. Most OTs will only see someone up to the age of 12, or sometimes 18, for sensory work.

    An AS diagnosis wouldn’t be enough for the insurance to cover it, because the current DSM-IV description of AS does not mention sensory issues at all. I have a motor dyspraxia diagnosis, and that’s one of three that the insurance company will accept. (I forget the other two.) Whenever SPD gets into the DSM-V, an SPD diagnosis will be sufficient, too.

  4. Kate says:

    I have an AS diagnosis and the insurance paid for me to see an OT when I was in Montana, but she wasn’t able to help me very much, or think of many things to do with me.
    Where in MA? Perhaps it’s near my grandparents. Man would I love to see her. What is the Thumper? It sounds fun.

  5. Rachel says:

    My OT is in Northampton, MA (which is in the western part of the state).

    The Thumper is a large massager that gives a very powerful “percussive” vibrational massage. It’s totally amazing and very grounding for me.

  6. Thanks so much for the information. I’ll have to find out what’s required of my insurance in the state of Indiana.

  7. Rachel says:

    An update on the insurance question: Hubby called the insurance company today on my behalf to ask about the progress of the referral authorization. He was told that we don’t necessarily need one. If we get the authorization, the insurance company will pay more, but the coverage is very good even without it. All we have to do is fill out a form and send in the bills. Since it’s much less of a hassle, we’re going to take the non-authorization route. We’re covered for 30 visits per year. Given that my OT’s recommendation was 12-16 visits, we’ll be fine.

  8. Stat Mama says:

    Rachel, your therapy sessions always sound so…pleasant! I’m glad you mentioned the therapeutic listening. My son’s Speech Therapist has recommended what I think might be the same program for us. The only problem is, they do not have a set to lend out, so we are trying to come up with the $500+ to purchase it. I’d be very interested to know how this is helping you, since I think auditory overload is definitely worst for everyone in our home.

    I really wish I could find somewhere that I could get OT. It’s great reading about your experiences with it, it really makes me feel hopeful.

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