Epilepsy Blog Relay: Whitney asks the hard questions about epilepsy clinical trials

by Whitney Petit | 0

This post is part of the Epilepsy Blog Relay™, which will run from June 1 to June 30, 2018. Follow along!

Whitney’s Story

My blog, Changing Focus: Epilepsy, is all about taking control of your life with epilepsy. I openly share my personal struggles and triumphs while providing tools to help you become your own best advocate for your health. Through this blog I want to show others that you can still live your best life, and how, despite the diagnosis.

Excerpt from Whitney’s blog

As technology and the advancement of patient care continues to move forward, a greater need grows for clinical trial participants and staff. Could the stigmatization against Clinical Trials innovation, be holding us back from a possible cure for Epilepsy? I want to breakthrough the stigmas so that we can get more patients involved, move forward to better quality care and get the meds or technology needed to successfully diagnose and treat epilepsy.

Don’t miss her latest post!

NEXT UP: Be sure to check out the next post by Emily at livingwellwithepilepsy.com.

TWITTER CHAT: Save the date for the #LivingWellChat on June 30 at 7PM ET.

Living Well With Epilepsy’s Epilepsy Blog Relay™ is an epilepsy awareness movement to designed to maximize collaboration and eliminate stigma. Thank you to our generous sponsors and partners!