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.
I’m still struggling to deal with the concept that living with epilepsy means there are going need to be recovery days.
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
I now know I need to question all the potential side effects a medication causes, even the rare ones.
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
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.
Jamie shares a story about her experience with seizures, pregnancy and epilepsy.
Michael shares how he feels isolated and alone since his diagnosis of epilepsy. He doesn’t know anyone else living with epilepsy.
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