Epilepsy Blog Relay™: Bailey on exercise and epilepsy
Day 3 of the Epilepsy Blog Relay focuses on exercise and epilepsy as a means to gaining independence while maintaining your safety.
Day 3 of the Epilepsy Blog Relay focuses on exercise and epilepsy as a means to gaining independence while maintaining your safety.
It’s time to shed the stigma of a disease that affects one in 26 people. Epilepsy is unbelievably common, yet few people know anything about it.
When I was first diagnosed I was in my early 20’s and didn’t really take my epilepsy too seriously. But two years ago I felt it was time for a change. I took better care of myself and became seizure free. That is until yesterday.
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.
Dana’s Post Epilepsy is a cause that is near and dear to my heart. For over 100 years, Epilepsy has affected our family in some way. It is a generational link that connects us daily into our past, present and future. Our familial Epilepsy has been passed down from my Great Grandfather … 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.
Soo writes the blog Soo’s Epilepsy Corner. Soo is living with epilepsy and has dedicated her efforts to raising epilepsy awareness.
Kathryn writes the blog, Kat’s Temporal Lobe Diaries. She writes, “I have seizures. It’s simply a part of my life, as much as every other thing.