Epilepsy Talk

Epilepsy Abuse and Civil Rights

November 3, 2015
4 Comments

The following letter was written to local Legislators, Health & Human Service Agencies, The Office for Civil Rights and selected members of the President’s Cabinet…

Dear President Obama:

Re: Epilepsy Abuse and Civil Rights


There’s a hidden artist inside you!

August 15, 2015
7 Comments

Maybe you’re an artist…actor…architect…painter…poet…philosopher…singer…or someone you just don’t know.

Because, quite simply, there’s another side to that electrical mischief that epilepsy produces.

Some types of epilepsy can spark inspiration, enhance creativity and bring out the latent artist in you.

It’s just waiting to be discovered…


VNS…Exciting News!

June 20, 2015
36 Comments

The Food and Drug Administration (FDA) has approved a new generator for the VNS Therapy® System.

The new generator, called AspireSR®, offers the ability to provide automatic stimulation in response to increased heart rate, in addition to its other stimulation timing.


I’m sorry I’ve been MIA

June 11, 2015
27 Comments

I had a concussion on Tuesday (my birthday!) and haven’t been very functional.

I’ll be back as soon as my eyeballs stop zooming. ☹

Thanks for being so wonderful and understanding. I appreciate it — and you — a lot.


Posted in Epilepsy

Celebrities Supporting Epilepsy

May 9, 2015
47 Comments

The names are probably familiar to you. But the fact that all of these people have epilepsy may surprise you. Despite that fact, they have lived their lives, becoming prominent in their fields, an inspiration to us all.


Famous Athletes with Epilepsy

May 2, 2015
10 Comments

There are many athletes who have overcome or gone on to surpass their epilepsy condition. They have strived, succeeded and provide an inspiration to us all. Along with some athletes’ outstanding commitment to epilepsy — advocating, teaching and supporting epilepsy.


On vacation until 4/6/15

March 21, 2015
8 Comments

My lap top connector broke, leaving me out of business.

See you on Sunday, April 6th…  😦


Posted in Epilepsy

Epilepsy: Art Therapy

March 14, 2015
11 Comments

A paintbrush is a powerful communication tool for experiences that are hard to explain in words.

It helps and allows your mind to wander without any restriction. The mixture of colors and the strokes define the inner feeling you want to express.

Your art is the extension of who you are, what you want and where you want to be. Your masterpiece, no matter how you made it, is priceless…


New! Helmets for Your Health

February 28, 2015
6 Comments

A pair of Swedish women have developed a remarkable solution for safety helmets: The Invisible Bike Helmet.

Tired of strapping ugly, uncomfortable styrofoam-and-plastic turtle shells to their heads, the pair came up with a revolutionary solution that does manage to give you full head protection without, remarkably, wearing anything on your head.

There’s also a new Inflatable Helmet. The airbag helmet is worn around the neck like a scarf or collar. The collar contains a folded up airbag that inflates in the event of an accident.

Sensors within the collar pick up strange or sudden movements. The airbag is shaped like a hood. It surrounds and protects the user’s head. (Natalie Portman wore one because of her character’s epilepsy in the movie Garden State!)

Then, of course, there’s lots more out there to choose from. And you can create your own personalized design…


Epilepsy Summer Camps

February 19, 2015
Leave a Comment

Below you’ll find a compilation of EFA summer camps and those supported by other organizations.
Ages range from 6 – 26, depending upon the camp and its activities.

Applications for this year’s summer camps are beginning. (Or starting very soon.) Dates and ages vary, depending upon the camp. So, it’s best you get the necessary info now, to avoid disappointment.

Camps should be contacted early for dates and applications.


« Previous PageNext Page »

    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.

    View Full Profile →

    To receive Epilepsy Talk articles FREE, simply go to the bottom of the right column, enter your email address and click on "Follow"

    Join 3,109 other subscribers
    Follow Epilepsy Talk on WordPress.com