Epilepsy Blog Relay: David on IEPs, 504 plans and the need for epilepsy awareness in education
When reviewing David’s son’s IEP, and earlier 504 plans the need for epilepsy awareness in education became painfully clear to this family.
When reviewing David’s son’s IEP, and earlier 504 plans the need for epilepsy awareness in education became painfully clear to this family.
Lili was diagnosed with Lennox-Gastaut syndrome (LGS), a rare and severe form of epilepsy, but therapeutic horseback riding was an activity she could enjoy.
Francesca’s Story: I have a type of epilepsy that was inherited from my mother’s mother. My grandmother was born with PCDH19 epilepsy.
Jes now writes Wishes for Mercy to inspire families battling epilepsy and to build supportive relationships within the special needs community.
Alison writes about stigma and epilepsy on her blog Shed Light on Epilepsy. In her recent post she encourages us to think about our epilepsy in a new way.
This post is part of the Epilepsy Blog Relay™, which will run from June 1 to June 30, 2018. Follow along! Andrea’s story When people see Andrea Menoudakis, whether it’s in a Youtube video or on stage with her rock band Motion Device, for the most part they will see one thing … Read More
This post is part of the Epilepsy Blog Relay™, which will run from June 1 to June 30, 2018. Follow along! Soo’s Story I live in Southern California and have had seizures all my life. I write Soo’s Epilepsy Corner to educate and tell my personal story. Excerpt from Soo’s blog We … Read More
This post is part of the Epilepsy Blog Relay™, which will run from June 1 to June 30, 2018. Follow along! Sharon’s Story Sharon Ross has a rare type of epilepsy. Though she has experienced seizures, the main impact the condition has on her life is her cognition. According to Sharon, her … Read More