I was contacted a couple of weeks ago by a writer for aolhealth.com. As I always say…any and all times we have the opportunity to talk about Epilepsy, it’s a good thing!

This is an open question for all of you with college-aged kids, or kids who are approaching college-age. What are your options? Have you consulted with your neurologist(s) regarding this question? Do you know of any universities or small private colleges with programs?

You can live a ‘normal’ life with Epilepsy.

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?

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

Once you get the ‘NO’ on surgery and you’ve experimented with multiple meds, is there anything left that will help you take back your life from a life of seizures?

How can you help those who will be diagnosed with Epilepsy just this year? Statistics show 200,000 people will be diagnosed in 2010. Those of us who live with the disease each day know what we are dealing with…but how about those ‘newbies’ to this life?

Switching doctors…or even getting a second opinion shouldn’t be something you fear. It’s a necessary part of your care.

Why won’t people talk about Epilepsy? Once they hear about the diagnosis, if they find out you might be on course for a major brain surgery…why do they all of a sudden tune you out?