Epilepsy Blog Relay: On Epilepsy and Stigma
Okay so I’ll be honest the topic of epilepsy and stigma is a bit of a bugaboo of mine. But I promise to spare you the soapbox today and make it interactive.… 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.… Read More
Epilepsy Blog Relay: How is epilepsy diagnosed?
The process of getting an epilepsy diagnosis can be slow. So dealing with this process requires patience, but here are a few things to expect.… Read More
Epilepsy Blog Relay: Does having one seizure mean you have epilepsy?
Does having a seizure have to mean you have epilepsy? Learn more about how the ILAE and doctors define epilepsy.… Read More
Epilepsy Blog Relay: Pushing the limits of my epilepsy
A few years ago, my family took a vacation that was not only relaxing, but gave me the chance to push the limits of my epilepsy in ways that surprised me.… Read More
Epilepsy Blog Relay: Ken’s Epilepsy Journey
With a traumatic childhood and multiple disabilities, Ken still fights for a better life and to help those around him.… Read More
Epilepsy Blog Relay: Handwritten note launches one family into the world of special needs
In searching through my son’s medical files I found a handwritten note written years ago. The note included tips for finding services our special needs son.… Read More
Epilepsy Blog Relay: Discovering My Epilepsy
Things are definitely still bumpy and new to me but I have found that the more educated I get and the more I indulge in the epilepsy community the better and more stable I feel. I have my own YouTube channel that until now didn’t feature much about my epilepsy but I’m not afraid to be a voice for others I have a passion to inspire! I know I looked and looked for youtube videos like the ones I make and am going to make for people just like me!… Read More