Epilepsy Blog Relay™: Abby and That Terrible Reminder
Abby’s Story: I was doing great. I hadn’t had a seizure in almost two years. But recently, I’ve changed my medicine.
Abby’s Story: I was doing great. I hadn’t had a seizure in almost two years. But recently, I’ve changed my medicine.
Maureen’s Story: I wanted to highlight a few epilepsy advancements I witnessed on my travels in Mahenge, Tanzania.
This post is part of the Epilepsy Blog Relay™ which will run from November 1 through November 30. Follow along and add comments to posts that inspire you! Health Insurance and Epilepsy Shopping for insurance can be overwhelming. There are so many things to think about: drug formularies, whether a plan covers … Read More
Tell the world about SUDEP Many people are unaware they are at risk of SUDEP or Sudden Unexpected Death in Epilepsy. That’s why SUDEP Aware, Living Well With Epilepsy and Lundbeck have joined forces to shine a spotlight on SUDEP Awareness Day, October 23. In fact, each year an estimated 1 in … Read More
For a grieving parent who has lost a child, the thoughts of an upcoming graduation day (and the day itself) – there are no words to express the pain.
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.
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?