Epilepsy Blog Relay™: A letter of thanks to caregivers
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.… Read More
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.… Read More
Casey felt vulnerable as a teenager with a neurological disorder, but now she is open about her epilepsy and raises awareness.… Read More
Epilepsy Education and Support is a dynamic Facebook page created to provide information and support for all those affected by epilepsy.… Read More
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!”… Read More
I started reading about diets and chronic illnesses but was skeptical of it all. I decided to change my relationship with food to better control my seizures.… Read More
Today’s post comes Audra Sisak who has recently learned she has aspergers. She’s changed her site from “his life with autism” to “our life with autism”.… Read More
Having both epilepsy and cerebral palsy, Colleen’s life began with so much uncertainty. As she’s gotten older, tech has played a key role in our life.… Read More
I turned to writing and learned to speak openly about epilepsy. Now, I have become someone who is much more confident. … Read More