Epilepsy Talk

Kid’s Medical Alert Jewelry That’s Functional And Fun

July 25, 2012
11 Comments

Just as grown-ups are reluctant to wear Epilepsy ID bracelets – even though they know they’re important, if not essential – kids are even more resistant. They’re “ugly, they’re dorky, they single me out” and they sure aren’t exactly something they’re crazy about wearing.

Well, we’re about to shatter that myth. Because there’s plenty of kids medical alert jewelry that’s not only functional, it’s stylish and fun!


Top-Rated Seizure Monitors

July 17, 2012
82 Comments

Peace of mind. A good night’s sleep. Safety and assurance.

Although these seizure monitors can’t make any guarantees, they can go a long way towards detecting danger. And maybe even saving a life.

Here are the most prominent models…


Charlie Rose: The Brain Series

July 9, 2012
4 Comments

Presented here is a roundtable of the finest minds in science, co-hosted by Nobel Prize winner Eric Kandel. Together, Charlie Rose and Eric Kandel interview brain researchers, scientists and doctors, talking about different subjects of the brain. Among them are scientific discoveries, advances in technology and cutting-edge treatments.

However, these thirteen episodes, also go much deeper. They discuss perception, consciousness, free will, decision-making, cognition, creativity, morality, emotion and memory.


2012 Most Recent Epilepsy Statistics

June 27, 2012
19 Comments

These numbers may scare you, depress you, or stir you into action. Whatever your reaction, they’re inconvertibility true. From the Institute of Medicine, via the Epilepsy Therapy Project itself…


Driving Laws by State

June 20, 2012
7 Comments

Every state regulates driver’s license eligibility of persons with certain medical conditions.

The most common requirement for people with epilepsy is that they be seizure free for a specific period of time and submit a physician’s evaluation of their ability to drive safely.

Another common requirement is the periodic submission of medical reports, in some states for a specified period of time and in others for as long as the person remains licensed…


Epilepsy in Twitter Times

June 4, 2012
10 Comments

Twitter is not our friend.

And the misconceptions and stigma of epilepsy live on.

A revealing study published in Epilepsy & Behavior provides evidence that the perception of epilepsy is not faring well in social media. Kate McNeil and colleagues from Dalhousie University in Canada analyzed data collected from Twitter to provide a snapshot of how epilepsy is portrayed within the twitter community…


Groundbreaking Report: A Giant Step for Epilepsy

May 16, 2012
6 Comments

In a special presentation from the Institute of Medicine (IOM), a groundbreaking report was released with 13 recommendations that the IOM designed to help improve care for all people with epilepsy…


Teen Epilepsy Support Groups

May 7, 2012
13 Comments

In recent years, support groups that cater specifically to teens with epilepsy have emerged, started by hospitals, religious groups, and affiliates of the Epilepsy Foundation. The number of support groups for teens with epilepsy is growing, but it is still small when compared to the many for adults with epilepsy and parents of children with epilepsy…


Children’s Brain Surgery…Preparing YOUR Child…

April 22, 2012
2 Comments

There is no “welcome” sign to the world of childhood brain surgery. And the resulting combination of fear, shock, and pain is almost too much to bear.

No amount of preparation or knowledge can help to ease or minimize the situation.

But preparing a child for surgery emotionally, is one of the most important things you can do. Surgery, without proper explanations and preparation, can traumatize a child…


Hugh Laurie Talks About It!

March 29, 2012
2 Comments

Hugh Laurie, star of the famous TV series “House”, talks about epilepsy awareness on You Tube, with honesty and candor…


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    About the author

    Phylis Feiner Johnson

    Phylis Feiner Johnson

    I've been a professional copywriter for over 35 years. I also had epilepsy for decades. My mission is advocacy; to increase education, awareness and funding for epilepsy research. Together, we can make a huge difference. If not changing the world, at least helping each other, with wisdom, compassion and sharing.

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