logo
OUR MISSION

OUR WORK

APPROACH TO
TREATMENT

PATIENT
PROTOCOL

HISTORY OF
RESEARCH

PRAGUE CONFERENCE PRESENTATION

PAPERS & JOURNAL ARTICLES

BOOKS

ONGOING & EXPANSION PROGRAMS

FAVORITE LINKS

ABOUT OUR STAFF
Donna J. Andrews, Ph.D.

Joel M. Reiter, MD

CONTACT FORM

 

 Visit Our New Favorite Links Page Below!

OUR WORK

Conservative estimates place the number of Americans with epilepsy at two percent of the population-at least four million people.  Of these, a minimum of one million have seizures which are not controlled with standard medical approaches.  Presently epilepsy is viewed as a functional disorder over which the sufferer has no control.  It is generally held that medications and surgical removal of damaged tissues are the only means of control and when these fail the individual becomes a member of the "hopeless" class, experiencing side effects of medications and difficulty in social and psychological adjustment.

This work began as a private investigation of the potential for a behavioral approach to the treatment of epilepsy.  Several disciplines were used for this investigation: neurology, psychiatry, psychology and biofeedback.  This first exploration in 1980 involved five patients with an average history of 15 years of uncontrolled seizures. Since then approximately 2573 people have been treated and the success rate for complete control is over 80%.

The Andrews/Reiter approach sees epilepsy as a behavioral disorder with functional symptoms.  The seizures are triggered by emotional reactions and stressful situations.  The seizures are not caused by damage to the brain.  Rather the damage has lowered the threshold at which the brain can no longer handle or recover from an Overload on its circuitry.  When the overload threshold is passed, a seizure occurs.  In some cases it may take weeks or even months to reach the threshold, in others as little as 30 seconds.  Instead of shutting down brain functioning through drug therapy to prevent seizures, a self-discovery process is implemented relating the personal responsibility of the individual to the occurrence of their seizures.  It minimizes or eliminates drug therapy, and reestablishes personal dignity by allowing the individual to achieve a normal and productive life.

Now our task is to make this information available to health professionals and people with epilepsy on a larger scale.  We are actively seeking community support and funding sources to continue and expand the work.

Previous page | Next page