Epilepsy Advocates Category
Get in the Game…to promote Epilepsy Advocacy
Epilepsy and SUDEP has become their mission with the Danny Did Foundation. And, they are doing a fantastic job. Their spirit and their drive to raise awareness and try to teach more people about Epilepsy and SUDEP in particular has truly inspired thousands of us!
Let Story of Accused Doctor be a Lesson for all of us with Epilepsy
An Oakwood Hospital (Michigan) pediatric neurologist has allegedly been diagnosing children, hundreds of them, with Epilepsy…FOR CASH. And these kids do not have Epilepsy.
More Epilepsy Advocacy…
Living with Epilepsy is featured in an upcoming episode of Health Corner on Lifetime.
Strolling for a Cure!
The Epilepsy Foundation of Michigan held their annual Detroit Summer Stroll for Epilepsy on Saturday, June 12, 2010 at the Detroit Zoo…what a day to reflect on those living with Epilepsy!
Stay Informed on how Health Care Reform will Affect you!
It’s time to discover how Health Care Reform will affect those who live with Epilepsy.
We all Must do our Part to Bring Epilepsy “Out of the Shadows”
The Epilepsy Community must united and help bring Epilepsy “out of the shadows.”
‘The Doctors’…and the Vagus Nerve Stimulator
‘The Doctors’ gave us a great opportunity to explore the option of the Vagus Nerve Stimulator (VNS).
What Exactly is a ‘Normal’ Life with Epilepsy? It’s a Matter of Opinion…
You can live a ‘normal’ life with Epilepsy.
Air Date for ‘The Doctors’ is set!
I’m speaking about the Vagus Nerve Stimulator (VNS) on the TV show, The Doctors, on May 19, 2010.
Sharing our Seizure Experiences to Boost Knowledge…
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.
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