DISCLAIMER:
The information contained herein is intended for
educational purposes only.
BE AWARE: The electrodermal testing devices have not been approved by
the Food and Drug Administration ("FDA") for assessment of nutritional
deficiencies, food allergies, the presence of toxins, Candida, Epstein Barr
virus, or the weakness of organs and glands. Use of the device for these
purposes is inconsistent with FDA approval. The galvanic skin response
device is a Class II device that may be used for
lie detection and for biofeedback.
There are no generally accepted completed
clinical studies which demonstrate that the electrodermal testing devices
are effective when used to assess for nutritional deficiencies, the presence
of toxins, food allergies, Candida, Epstein Barr virus, and the strength or
weakness of organs and glands.
Your child's exposure to lead or heavy metals cannot be determined
solely through electrodermal testing.
You should not make decisions about your or your child's health and
nutritional needs from information obtained solely through electrodermal
testing.
You are
to discuss all CEDS recommendations with your health care provider before implementing
any of them.
There are medical tests for many, if not all of the issues that
respondents use electrodermal testing to assess, and you
are strongly encouraged to confirm the exposures identified through standard
medical testing if you or your family physician feel that it is
necessary.
Laws regarding this equipment vary from country to
country.
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