Vaso-Vagal Discussion

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Re: Vagas Nerve Stimulator

From: George Perricone Jr.
Date: 12/13/00
Time: 12:39:33 PM
Remote Name: 198.26.132.99

Comments

Dear Sissy, My name is George Perricone Jr. I was hoping you might have learned something about the vagas nerve stimulator. The reason I ask is that my older sister suffers from cerebral palsy for the last 23 years of her life. She has gone from one medication to the next and now her body has seemed to have built up a resistance to the drugs. My family and I are trying to see what other measures that we can take and the stimulator was one option. If you could please send me an e-mail back at

perriconeg@mcrdpi.usmc.mil

The e-mail address might seem strange only due to the fact it is my work e-mail and i am a Marine. I appreciarte the time you have taken in reading this Respectfully, George Perricone Jr.

This web site is not a substitute for a thorough medical evaluation and diagnosis of your vaso-vagal type symptoms.  Medical treatment and diagnosis is the only acceptable initial response to these serious symptoms since they might present from any number of life threatening and treatable illnesses. It is for you and your physician to rule out more serious illnesses; Please don't use this online forum as an alternative to getting responsible medical attention and being under the care of a physician for the duration of any unknown, suspected or dangerous vaso-vagal syndrome symptoms.

Last changed: June 22, 2007