Epilepsy Talk

Epilepsy — Top Financial and Medical Assistance Programs

March 19, 2019
1 Comment

With so many people at the end of their resources, we could all use a helping hand.

Below is my attempt to research viable resources for financial and medication aid.


Epilepsy, Anxiety and Depression

April 17, 2018
33 Comments

One study stated that 80% of the patients with epilepsy were also diagnosed as having a depressive disorder.

Upwards of 60% of these individuals had a history of significant episodes of depression.

And 10-32% experience symptoms of anxiety.


Autism — Who Has It?

August 29, 2015
15 Comments

The autism rate has increased — 1 in 68 kids are now identified with the disorder. 20-30% of children with Autism Spectrum Disorder (ASD) develop epilepsy. And children whose language skills regress before they turn 3 have been found to have a higher risk of developing epilepsy.


Wrong Diagnosis?

March 2, 2014
9 Comments

There are many ways that your medical care can go wrong. All of the phases from diagnosis to treatment can have some type of error.

Studies of error types: An Institute of Medical Report attempted to quantify the types of medical errors that occur in healthcare settings.

One cited study lists causes of errors as follows:


Epilepsy: Meditation vs. Medication

December 21, 2013
29 Comments

You can have medication without meditation. Most of us do.

You can do meditation without medication. Most of us wouldn’t and shouldn’t take that risk.

But together, they can enhance one another.


Where to Go When You Need Help — Directory of Epilepsy Resources

November 21, 2013
6 Comments

Here are some wonderfully useful links I’ve found along the way. Some may be familiar and some may be new to you. If you have any additions or suggestions, please, speak out…


Epilepsy and Anesthesia

August 4, 2013
20 Comments

Anti-epileptic drugs (AEDs) cause unique considerations for patients with epilepsy because skipping, or even delaying a single dose, can result in seizures.

Strategies for avoiding or minimizing skipped doses are paramount in the care of patients with epilepsy.


No-Cost or Low-Cost Drugs and Patient Assistance Programs

May 23, 2012
9 Comments

Today, things are constantly changing. Especially when it comes to epilepsy medications and resources.

Some companies have expanded their programs or even offer new ones. Others have cut their funds, and sadly others have ceased to exist.

Here’s a new and comprehensive list…


    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 →

    Enter your email address to follow this blog and receive free notifications of new posts by email.

    Join 2,593 other followers

    Follow Epilepsy Talk on WordPress.com