Epilepsy Blog Relay: New epilepsy diagnosis after seven years
After seven years of struggling to get a proper epilepsy diagnosis, Laura found a neurologist who would listen. She’s now a year seizure free!
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!
After seven years of struggling to get a proper epilepsy diagnosis, Laura found a neurologist who would listen. She’s now a year seizure free!
Caroline has found that managing her epilepsy has allowed her to be true to herself and focus on the creative work she is passionate about.
Amanda’s passion has always been to be a writer, and more specifically a journalist. She shares her adventures and stressors when dealing with her epilepsy as this soon to be graduate searches for hope.
5 things my cancer diagnosis taught me about how to live better with epilepsy.
If Epilepsy has taught me anything, it’s that changing my goals is not failing. I had an absence seizure while driving on the freeway. I am more hopeful because my best friend Emily loves me despite the accident.
Early on, Soo’s family would not use the word epilepsy in their home. Now, she is an advocate and makes the most of her local epilepsy support group.
Amber shares her story of brain surgery and brain tumor related epilepsy. She shares her struggle to find hope and create a life despite her challenges.
Chantal has been battling epilepsy for 19 years with the help of VNS. She shares a recent letter to her epilepsy.