Epilepsy Talk

Antidepressants — Improving Mood AND Seizure Frequency

May 19, 2013
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Epilepsy and depression often go hand-in-hand. Up to 50% of people who have epilepsy also experience depression at some point in their lives, and this greatly impacts upon their quality of life.

The highest frequency rate occurs in those patients with seizure disorders arising in the temporal or frontal lobes or who have poorly controlled epilepsy. And among TLE patients, those with a left temporal focus had higher depression severity than those with a right focus. A more recent study confirmed these findings and found that patients suffering from a complex partial seizure disorder were much more inclined to have depression, compared to those with generalized tonic-clonic seizures.

However, concern for the potential of certain antidepressants to induce seizures has led to under-treating depression and anxiety disorders in epilepsy patients.


From AEDs to Surgery and Beyond…Some Options Explained

May 12, 2013
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The saying “there’s something for everyone” may be true. But with epilepsy, it’s often a dicey proposition — not to mention frustrating — to determine what that “something” is for you.

Anti-Epilepsy Drugs

No, they’re not for everyone, and sometimes it’s like going on a non-stop merry-go-round (dizziness and all), but when you’re lucky enough, you can find your “magical medicine mix”.

Here are some interesting facts…


Responsive Neurostimulation (RNS) Shown to Reduce “Untreatable” Seizures

May 5, 2013
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The idea that we can implant a Star Trek-type device that will detect seizures and interrupt them without causing injury is entirely new. And exciting. And scary.

Especially for those people with epilepsy that have seizures that begin at one focal point in the brain, but aren’t appropriate for epilepsy surgery.


Epilepsy and Neuroengineering — A Brave New World of Possibilities

April 28, 2013
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Traditionally, the mainstay of epilepsy therapy has been treatment with antiepileptic drugs (AEDs).

But for 30% of those affected, no combination of standard therapy — medications and/or surgery — can control their seizures.

Although more new AEDs have come to the market over the past 10 years than during any other time in history, their primary contribution has been to improve adverse effects of medication, rather than to make more people seizure-free.

The proportion of people with epilepsy worldwide — whose seizures cannot be controlled by medical therapy — has remained unchanged, despite all these new pharmaceutical interventions…


What were your most formative moments?

April 21, 2013
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For me, it was three different stages, ages and issues…


Gratitude is the Attitude — Part 6

April 16, 2013
40 Comments

A wise woman once told me: “When you wake up in the morning — before you get out of bed — think of 5 (or 10!) things that you’re really grateful for.” (I think 10 is a bit of a stretch.)

That simple advice, changed my attitude. And my life…


What’s been your greatest success?

April 15, 2013
25 Comments

For me, it’s living…


“Pseudo Seizures” AND Epilepsy – Yes You CAN have BOTH!

April 8, 2013
9 Comments

Some know it as non-epileptic seizures (NES), psychogenic non-epileptic seizures (PNES), or pseudoseizures. And then there’s epilepsy. Which is what?


Attractive Epilepsy Alert Jewelry

April 8, 2013
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Here are some great resources for Medical Alert jewelry that’s both functional and fun…


TNS vs. VNS – NO SURGERY!

April 1, 2013
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The first Vagus Nerve Stimulator (VNS) was implanted in 1988, as a therapeutic option for medically intractable epilepsy, when elective epilepsy surgery was not appropriate.

As the number of implanted vagus nerve stimulators grows, so does the need to remove or revise the devices.


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    About the author

    Phylis Feiner Johnson has been a professional copywriter for 30 years. She also spent 20 years with epilepsy. She writes from the heart to increase education, awareness and funding for epilepsy research. For further information, contact The Epilepsy Foundation of Eastern Pennsylvania at http://www.efepa.org/ and please make a contribution to become an advocate, too.

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