Epilepsy Blog Relay: Michael takes a positive approach to an epilepsy diagnosis
After years of mental and physical trauma from seizures, Michael discovered what he wanted to acomplish as a person, and as someone diagnosed with epilepsy.… Read More
After years of mental and physical trauma from seizures, Michael discovered what he wanted to acomplish as a person, and as someone diagnosed with epilepsy.… Read More
Leila attended her first PAME conference and found it was a meaningful way to connect with others in the epilepsy community to discuss SUDEP.… Read More
Allison is shedding light on epilepsy one aura at a time. … Read More
Like many people diagnosed later in life, Jewel had little knowledge of what Epilepsy was, and what life would be like living with it.… Read More
On 6/30 at 7pm ET, we will host our next #LIVINGWELLCHAT. We will hear from the community on what the new marijuana-based epilepsy drug could mean for families affected by LGS and Dravet Syndrome.… Read More
I suffered a series of tonic clonic seizures on the day my daughter graduated from college, which also happened to be my birthday. … Read More
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.… Read More
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.… Read More