Epilepsy Talk

Coronavirus (COVID-19) — How To Get Instant Care

March 30, 2020
27 Comments

You wake up and you’re feeling crummy. You have a fever. You may be coughing. But because of the Coronavirus, your physician isn’t available. You panic. In most states, you cannot even be tested for COVID-19.

It takes between 2 and 14 days for a newly infected person to start showing symptoms.

After symptoms begin to show, it can take more than a week for them to be eligible for testing (many people are not eligible at all).

And then, thanks to backlogs in testing availability, it can take days for them to learn they tested positive.

Maybe you should go to Urgent Care. But they’re so overloaded, they might turn you away.

Emergency rooms won’t accept you unless you’re have a very high temperature and having trouble breathing.

That’s when they will take you and put you on a ventilator. But what happens in between? Panic or medical care from an unexpected source?


Epilepsy & Migraines — Kissing Cousins

March 18, 2019
17 Comments

A strong relationship between migraines and epilepsy has long been suspected.

But now it is fact, according to extensive research cited by Steven Karceski, MD in Practical Neurology Magazine.

The International Headache Society (IHS) criteria divides headache disorders into two main groups, with similarities to groups of epilepsies:


Have You Had A Concussion?

March 30, 2014
34 Comments

In a fraction of a second, head trauma can dramatically change your life.

It can be a boink on the head, a fall, sports activities, or a car accident — among many other possibilities.


Epilepsy and Encephalitis

September 18, 2013
39 Comments

Imagine an inflammation so powerful that it can play havoc with your brainstem, cerebrum, cerebellum, spinal cord, and peripheral nerves.

That’s the neurological damage that can happen as a result of encephalitis.


    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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