It’s back to school time…When it comes to sending your child with Epilepsy to school, you shouldn’t feel alone. There are many resources that can help.

Tucket was Andrew’s dog, through and through, but in January 2003, when I became sick and began this journey called Epilepsy, Tucket really became ‘my’ dog. We always marveled at how he could sense seizures. He was not trained to be a seizure alert dog, but he has this amazing quality. He climbs into my lap when my auras begin, sometimes even tugging at my clothes so I know to sit down on a piece of furniture if I’m standing.

As for my child, I pride myself on the fact that she has just as normal a life as her friends and classmates, and I work very hard at this. Does her mother have seizures? Yes, but she is cognizant of that and she knows how to react. I surround myself with people who understand and care, from my husband to my very, very close friends. So, I never worry that she is deprived of love and attention.

A neurologist in Detroit is accused of misdiagnosing hundreds of children…telling them they had Epilepsy. It turns out, they don’t. He prescribed medication for virtually all of them, brutal and terrifying anti-seizure medications.

Regarding the aolhealth.com post last week, I heard from SO many readers, both new and old…and your compliments were very encouraging, not to mention, welcome! I also received lots of advice, questions and words of encouragement. It’s why I’m doing what I’m doing with this blog!

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!

In a new study, researchers found an increased risk of suicide, attempted suicide or “self-harm” only among current users of certain newer medications that had previously been linked to a risk of depression.

Why don’t more people ‘Talk about It’? In other words, why is it so difficult to speak freely and honestly about Epilepsy and seizures?

Epilepsy Advocate and Healthy Women have launched a new campaign to focus on women living with Epilepsy.

Epilepsy advocates come in many different varieties. They can be those of us who live with Epilepsy, family members or good friends of those with Epilepsy, doctors and others in the medical field who deal each day with Epilepsy…or simply people who understand this complex world, and care.