I’m speaking about the Vagus Nerve Stimulator (VNS) on the TV show, The Doctors, on May 19, 2010.

The more conversations we have about Epilepsy and seizures and the more realities we share, the more we raise awareness. If you’re like me and have seizures, I learned so much from others and their seizures.

The overall goal of tracking seizures is to find a pattern, the seizure triggers and the length and severity of seizures to make sure you are being treated properly.

Now that my daughter is 4 1/2 years old, I’ve begun to feel that sense of guilt. Does my epilepsy affect her life?

The more we talk, the more people will learn. Advocacy and support is so crucial if we want to erase the stigma and inform those who don’t know a thing about Epilepsy.

Medication Switching…in other words, you take your prescription to the pharmacy and the pharmacist fills it with a generic anti-epileptic medication instead of the name brand, has become such a crucial issue for the Epilepsy Community.

An interview with Dr Brien Smith of Henry Ford Hospital and Greg Grunberg, Epilepsy Advocate…on what’s new and important in the Epilepsy world

It’s Friday…time for some updates and new information!

A new study released by doctors at the Mayo Clinic says newspaper coverage of accidents involving people with Epilepsy is biased.

A film aired last evening on PBS, Through the a Dog’s Eyes, which profiles Canine Assistants. They provide service dogs to those in need, including some people with Epilepsy.