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.