~Epilepsy in Real Life~
My life revolves around it. Me- singularly. If I close my eyes… No husband, no child, no job, no… whatever. Music. Any of you relate? There’s a song always for my mood. And I’ll play it- OVER and OVER- til my husband’s shaking his head and pleeeeeading for the repeat button to break. lol It’s... Continue Reading →
So this weekend, in fact today, Friday, October 6, my husband and I were supposed to attend The RiSE festival outside of Las Vegas… Something I had been looking forward to for months and months since I purchased our tickets. It's supposed to be a time to come together with music, but most importantly, a message...
Maybe you’re new to Epilepsy and in that case, one of my usual posts depicting daily life or the continual struggles/side effects would be most helpful. However, today is short and sweet for once. I welcome the newbies but I’m talking to the “old timers,” whether Epileptic yourself or a caregiver...
You know that song… the one you put on repeat for hours, days, months straight. Yep, this is one of mine. I literally get sad when it ends. Partly because I remember the story behind it from a particular movie’s soundtrack and also just because I feel like running, jumping, laughing and spinning all at... Continue Reading →
In Megan's Shoes 