Epilepsy Blog Relay: On Recovery Days
I’m still struggling to deal with the concept that living with epilepsy means there are going need to be recovery days.
Epilepsy Blog Relay: Epilepsy and Brain Training
Similar to nutrition and religion, I am not necessarily a model to follow when it comes to making great life choices. I mean, I’m getting better at the whole adulting thing for sure, but it’s taken me longer than I’d like to admit to get to this point. So bear that in … Read More
Epilepsy Blog Relay: On the importance of questioning side effects
I now know I need to question all the potential side effects a medication causes, even the rare ones.
4 Common Epilepsy Side Effects and Tips on How to Deal with Them
Rachel on epilepsy side effects I thought I might cover a few specific epilepsy side effects that I have suffered and how I have learned to cope. I have to state here, this is how I have dealt with these side effects, and my solutions may not work for you. Also, some … Read More
Epilepsy Blog Relay: Dave shares his story as a father of a child with a disability
Dave shares his story as the father of a child with a disability in hopes that his words help other people who are on a similar journey.
Epilepsy Blog Relay: Seizures, pregnancy and epilepsy in real life
Jamie shares a story about her experience with seizures, pregnancy and epilepsy.
Epilepsy Blog Relay: Tips to feel less isolated and alone after an epilepsy diagnosis
Michael shares how he feels isolated and alone since his diagnosis of epilepsy. He doesn’t know anyone else living with epilepsy.
Epilepsy Blog Relay: A system of support
This post is part of the Epilepsy Blog Relay™ which will run from March 1 through March 31. Follow along! Soo Ihm has lived with epilepsy since childhood. Now in southern California, she writes the blog Soo’s Epilepsy Corner and is an advocate for epilepsy awareness. She enjoys playing the piano, going to art museums, … Read More