Thursday was full of ups & downs with seizure activity:( When you live with Epilepsy, and especially when uncontrolled, you are told to...

Epilepsy Awareness Month comes to an end, but for our family, the battle is 12 months of the year. Our family journey we thought was...

How logo & title came about go my FB page & Blog page I get asked often by many why I just don't say "Marissa's Epilepsy story" or the...

September 5, 2022 19th Wedding Anniversary = Beyond blessed First off I cannot thank everyone enough that reached out in various ways to...

November is a month dedicated to raising Epilepsy Awareness across the globe. #Epilepsy according to the Mayo Clinic publication 2021 is...

Why not spread your family or friends #MyGlitch Awareness with a little fun in decorating and or painting your pumpkins purple. It's fun...

SUDEP is a very scary term to many individuals and families live with on a daily basis. Many times those that live with their own...

This may sound crazy to many of you, but today (October 14th) would have been my Nannie's 105th Birthday and she must of thought I needed...

Every person that is diagnosed with Epilepsy has their own "Glitch". I want people to understand just because some forms of Epilepsy can not be seen (it's known as an invisible disability), it does NOT make it any easier. It is extremely hard physically, emotionally and mentally. THERE IS NO CURE! There is only controlled or uncontrolled Epilepsy. This is why it is very hard on the the individual, but it's just as hard on the rest of the family/support system. It truly is