Epilepsy Blog Relay™: A Day in the Life of an Epilepsy Blogger
People often ask what it is like to blog about epilepsy. Here is a day in the life of a PAME Conference blogger and attendee.
Living Well With Epilepsy’s, Epilepsy Blog Relay™ is an epilepsy awareness movement to designed to maximize collaboration and eliminate stigma. Thanks as always to our generous sponsors and partners!
People often ask what it is like to blog about epilepsy. Here is a day in the life of a PAME Conference blogger and attendee.
Happy Father’s Day to you Dave, and also to all the great dads like you who put their child with special needs first. You are all great dads.
The top of the waterfall in Iceland was just as beautiful and tranquil as described, perfectly reflecting this newfound sense of peace I had found.
Try not to give in to other people’s beliefs of you. You are in control. You are in charge of how you see yourself.
I used to have a block against connecting with people that had Epilepsy. These days I’m more accepting of my Epilepsy and I’ve found people who understand.
I love it when people say, just find the right balance. It sounds so simple. But, is it really?
Stigma can make you feel ashamed, embarrassed and it can make you lose your confidence. Try to remember that you are not your condition.
Epilepsy is one of the most common conditions affecting the brain yet there is still a stigma associated with epilepsy. Could sharing personal stories create a tipping point to change the dynamic?