Epilepsy Talk

Clinical Trials. YES or NO?

February 10, 2011
6 Comments

If I was asked to take part in a clinical trial, I’m not sure what I’d say…

First there is the fear factor. Would I be a guinea pig for something dangerous? Would they take away my medicines? Would it hurt me? Would it change something in me?

I asked those very questions to Patient Advocate David Albaugh at Team Epilepsy. http://www.teamepilepsy.org/

Here’s what he had to say…


Your Child Has Just Been Diagnosed With Epilepsy…

January 23, 2011
8 Comments

The diagnosis comes in. It’s epilepsy.

Your heart drops to the bottom of your stomach. You may panic…or cry…or call in the troops for support.

Whether your child is an infant, toddler, grade schooler, adolescent or young adult, how you behave now will make a world of difference to their future.

Here are some resources to help you help your child…


Two Tests Could Aid in Risk Assessment and Early Diagnosis of Alzheimer’s

January 19, 2011
6 Comments

From “The New York Times”, published January 18, 2011…

“Researchers are reporting major advances toward resolving two underlying problems involving Alzheimer’s disease: How do you know if someone who is demented has it? And how can you screen the general population to see who is at risk?…”


The Sacred Disease. A Movie You Can Not Afford to Miss…

November 28, 2010
4 Comments

The Sacred Disease is a movie you can not afford to miss…

Motivated by lack of funding and awareness for epilepsy, this film covers the full spectrum of what it’s like to live with this neurological condition by following the lives of three individuals. The Sacred Disease displays an intimate portrayal of the complexities and daily difficulties faced by people with epilepsy.


There IS Hope!

November 15, 2010
7 Comments

There IS Hope!

Here is an encouraging letter I received from the Department of Health & Human Services:

Thank you for your personal message regarding the training of law enforcement officers and other public safety personnel who respond to people experiencing epileptic seizures…


Let’s Educate Candidates for Congress about Epilepsy!

October 7, 2010
5 Comments

Take Action: Let’s Make Epilepsy an Election-Year Issue!

Election Day is less than a month away and candidates are paying close attention to what voters have to say. This gives us a great chance to educate them about epilepsy, the need to find a cure, better treatments and stopping discrimination in schools and at work.

Click on this URL to take action now
http://capwiz.com/efa/utr/2/?a=18239501&i=94296635&c=
or copy the entire URL and paste it into your Web browser.


Increase in Seizures Seen in Kids With H1N1 Flu

September 23, 2010
10 Comments

MONDAY, Sept. 20 (HealthDay News) “Children made ill by the 2009 pandemic H1N1 swine flu virus suffered more seizures and other nervous system problems than those with seasonal flu, a new report reveals…”


UPDATE: AED Suicide Risk…

August 25, 2010
12 Comments

July 28, 2010 Medical News Today

“While the Food and Drug Administration (FDA) requires a warning of an increased risk of suicide for all epilepsy drugs, a new study shows that only certain drugs may increase the risk. The study is published in the July 27, 2010, issue of Neurology®, the medical journal of the American Academy of Neurology…


Brain Injured Solders Still at Risk for Epilepsy Years Later…

July 24, 2010
1 Comment

A new study, published in the medical journal of the American Academy of Neurology, highlights that soldiers who have suffered traumatic brain injuries associated with the wars in Iraq and Afghanistan are at a significantly high risk of developing epilepsy even decades after the brain injury occurred.


Vimpat For Uncontrolled Partial-Onset Seizures

July 20, 2010
8 Comments

A recent multi-center study has confirmed earlier study results that 400 mg/day of Lacosamide (Vimpat) provides a good balance of efficacy and tolerability for patients with uncontrolled partial-onset seizures (POS), and doses of 600mg/day may provide additional benefit for some patients.


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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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