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In order to be able to function normally, our bodies must maintain a number of different systems in a state of balance, called homeostasis. This internal regulation affects body temperature, blood pressure, heart rate, respiration, and internal levels of stimulation. With an SPD child or adult, if stimulation is too great, it results in stress to the body. If too low, the child or adult falls into a state of sensory deprivation. There is scientific evidence suggesting that in order to function at an optimum level, we all need a certain level of stimulation that is neither too high nor too low. With an SPD child or adult, their nervous system seems unable to easily and automatically regulate and manage these levels. When not working properly, the individual feels compelled, not even being aware of it, to seek sensory input. In seeking sensory
stimulation, people tend to go to the sites where there are many nerve
endings. Hands, feet, mouth and the scalp are common places. Many different
behaviors could be used to perform this balancing function externally.
Hair pulling, skin picking, nail biting, cheek biting, nose picking,
*grin* are only a few of many that I have seen. While any or all humans
may engage in these behaviors sometimes, the difference with SPD kids and
adults, (whose behaviors have become extreme versus those who are doing
them on occasion) are that they have considerable difficulty regulating their internal levels
of stimulation, and are utilizing these methods for self-stimulation or
self-soothing. Why this could be helpful to an internal state of regulation to satisfy both, or either, under- and over- stimulation comes with the understanding that each type of stimulation is the polar opposite of the other on a continuum of sensory stimulation levels. It can be either soothing... or stimulating, and bring about changes and more balance to internal regulation. What to do? Is it becoming too much, destructive even? If this person has already been diagnosed as an SPD child or adult, I would recommend speaking to their therapist. Ask him/her about better ways to learn to self-regulate. Find other, less destructive sources of stimulation. There are medications that have been used to help in severe cases. Consult with a physician concerning that. There are also emotional, and even environmental reasons a person may be hair pulling. If this person is not already under the care of an Occupational Therapist, I would suggest beginning with Michele Mitchell's comprehensive SPD Checklist for Children, or Adult and Adolescent Checklist to determine if an evaluation is needed. One of the methods I like to
see, is when we teach our SPD kids and adults to discover and identify how
they are feeling. To recognize when they are over or under stimulated.
Then work together to find activities, with each of the senses, to "feel
better". The program How Does Your Engine Run?: Leader's Guide to the Alert Program for Self Regulation, Revised Edition Providing preventive methods, such as decreasing sensory overload, as needed, to balance internal regulation when feeling the need for less stimulation, or as when overwhelmed and stressed, by providing calming activities to soothe. Conversely, adding more sensory stimulation when seeking, or craving more. The hair pulling habit itself can be difficult to overcome, but I have seen great improvements, by offering different choices of stimulation. This is the most common method I have seen utilized - substituting other forms of stimulation to replace unhealthy, destructive or unsafe activities.
Copyright © 2007 Michelle Morris. Reprinted with permission. _____________________________________________________________
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