Epilepsy Blog Relay™: A lifetime of epilepsy challenges
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
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
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
This post is part of the Epilepsy Blog Relay™, which will run from Nov. 1 to Nov. 30, 2017. Follow along! Hadley Jo’s Story Hadley Jo (4) was diagnosed at age 2 with cryptogenic localization related epilepsy. According to the journal, Epilepsy & Behavior, up to one-third of children with epilepsy are diagnosed with … Read More
Nicholas was diagnosed with infantile spasms at 6 months of age. Doctors were able to control his seizures but recently they have started back up.… Read More
Emily has a positive outlook regarding epilepsy and despite living with absence seizures she has become an outspoken advocate sharing hope with others.… Read More
When I was diagnosed with Epilepsy at the age of six, my life transformed into a monsoon. I started having trouble socially, academically, and physically. It seemed as if my world was in a downward spiral until I was introduced to softball. That is where I learned that giving up was never an option.… Read More
This post is part of the Epilepsy Blog Relay™ which will run from June 1 to June 30, 2017. Follow along! For the blog relay this month, I wanted to provide another perspective. By now, you know mine. Epilepsy sucks. It’s a challenge… all. the. time. But, I always try to remember … Read More