Clinical Trials and Epilepsy: Innovation that Matters

As technology and the advancement of patient care continues to move forward, a greater need grows for Clinical Trials, participants, and staff. Could the stigmatization against the innovation of Clinical Trials be holding us back from a possible cure for epilepsy? Read More

7 Questions to Ask Your Doctor When Diagnosed with Epilepsy

I encourage you to be your own best advocate. Don’t be afraid to ask questions. Don’t wait until the appointment is over and wish you would have said something or got that burning question in. Read More

Build the Best Healthcare Team: For You

Living with Epilepsy, or any chronic illness, requires you to have the best healthcare team available. Finding these physicians are not always easy. Referrals, research, office visits, testing, its like an unending cycle just to find someone that suits you and your needs. Read More

How Television Portrays Epilepsy

This post is part of the Epilepsy Blog Relay™ which will run from June 1 through June 30. Follow along and add comments to posts that inspire you! Every time I hear the word “seizure” during a television show I automatically start to cringe. How will it be displayed this time? Will it be a Read More

Love Thy Neighbor #GivingTuesday

On one occasion an expert in the law stood up to test Jesus. “Teacher,” he asked, “what must I do to inherit eternal life?” “What is written in the Law?” he replied. “How do you read it?” He answered, “ ‘Love the Lord your God with all your heart and with all your soul and Read More

Advocate to Educate

Over the last few weeks countless tweets, Instagram comments and emails have been pouring in stating “I want to advocate more”, “Thank you for being such a great advocate” or “How do I become an advocate for epilepsy?”. I’ve even gotten a few text messages from a close friend with epilepsy stating she sucks at Read More