Epilepsy Advocates Category

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.

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.

For those of you around the world, if you’ve never participated in a gathering or fundraiser for your local Epilepsy Foundation, I highly suggest it! It’s very easy to do, and not only will your Epilepsy Foundation benefit, but you stand to gain so much!

A film done to honor Evan Moss and his life with Epilepsy, just won the top prize at the Neuro Film fest and the Fan Favorite Award.

Meet an incredible Epilepsy advocate…a Mom who lost a child to Epilepsy.

So often, we all get wrapped up in communicating through social media outlets and spreading the word about Epilepsy via chatrooms. Are we caught up on the news about the disease?


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