Keeping it All Together: Life as a Caregiver

Caregivers of people with epilepsy are the unsung heroes at the heart of a successful treatment plan. Read about three different caregivers and learn strategies for survival in managing the stressful but fulfilling job of a caregiver.

Lisa Loiodice: In My Own Words

The In My Own Words
column gives people whose lives are affected by epilepsy the chance to share experiences and solutions to their problems. This is Lisa's story. Our hope is that it will inspire others.

^{By Lisa Loiodice, Special to EPILEPSYUSA}

Dylan’s Journal: Life with epilepsy in the words of an 8-year-old

Dylan Loiodice writes in his journal to express his frustrations and victories in dealing with epilepsy day to day.

^{By Dylan Loiodice, Special to EPILEPSYUSA}

Coffee Break

How one Starbucks barista with epilepsy found support and encouragement on the job.

^{By Morgan Murphy, Special to EPILEPSYUSA}

How to Talk to Your Family About Your Epilepsy Diagnosis

Taking the stigma out of epilepsy is the first step in helping a loved one understand your condition.


^{By Anne L. Fritz, Special to EPILEPSYUSA}

Summer Camp

An awesome adventure for the kids and well-deserved respite for parents.