Epilepsy Blog Relay™: Jessica on ‘Wishes for Mercy’
When our daughter was first diagnosed we were told that epilepsy would be easy to manage. Two years later and that has not come true.
When our daughter was first diagnosed we were told that epilepsy would be easy to manage. Two years later and that has not come true.
Exploring Hawaii, and the Kaumana Caves, reminded me how many new experiences can seem overwhelming yet are worth it in the end.
As a mom to a child with epilepsy, I want to hold him in my arms and make it all go away. This is when my pharmacist hat comes off.
Soo writes the blog Soo’s Epilepsy Corner. Her site has been growing steadily for the past three years.
Danielle’s letter of thanks: When I was diagnosed with Epilepsy 6 yrs ago, a lot changed. I’m glad I had all of you there for me every step of the way.
Casey felt vulnerable as a teenager with a neurological disorder, but now she is open about her epilepsy and raises awareness.
Epilepsy Education and Support is a dynamic Facebook page created to provide information and support for all those affected by epilepsy.
Gail’s Story: I’ve had epilepsy for over 45 years. I have grand mals and petit mals. I asked if seizures change over your lifetime and my doctor said “Yes!”