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Epilepsy Blog Relay: Diminishing the Burden

This post is part of the Epilepsy Blog Relay™ which will run from March 1 to March 31, 2018. Follow along!

Jade’s Story

I was diagnosed with Epilepsy 30 years ago at the age of eight. The word burden was not part of my vocabulary all those years ago when this journey with Epilepsy began. Yet by the time I entered my twenties burden was all I felt. This was never a feeling my family put upon me and nothing I felt as a child. As I grew up and learned firsthand about medication costs, insurance struggles and personal sacrifice. I could see what my family had to deal with. With age brought a different understand of my diagnosis and it shifted everything for me. I had always been determined to be independent and self-sufficient but I felt even more so with age.

Read Jade’s Post


NEXT UP: Be sure to check out the next post by Allison at http://www.shedlightonepilepsy.org/. For the full schedule of bloggers visit livingwellwithepilepsy.com.

TWITTER CHAT: And don’t miss your chance to connect with bloggers on the #LivingWellChat on April 2 at 7PM ET.

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