Epilepsy Blog Relay: Maureen vacations where epilepsy is considered a curse
Counting pills a gazillion times before a vacation might seem over the top, but if Maureen doesn’t have her epilepsy medication she will have seizures.
Epilepsy Blog Relay: Tips on creating 504 and IEP plans to safeguard your child with epilepsy
Audra offers some tips on creating a 504 and an IEP plan to safeguard your child with epilepsy at school.
Epilepsy Awareness Month 2018: What you need to know
November is Epilepsy Awareness Month and it’s a great opportunity to get people talking about a disease that affects between 1-3% of the world’s population.
Living Well Outside: July will be all about getting outside
Throughout the month of July, we’ll be making time to get outside. All month we will be celebrating the ways you are #livingwelloutside.
LIVINGWELLCHAT on CBD, Medical Marijuana and Epilepsy: June 30 at 7pm ET
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.
FDA approves Epidiolex, first medication derived from marijuana
FDA has approved Epidiolex for the treatment of seizures associated with two rare and severe forms of epilepsy, Lennox-Gastaut syndrome and Dravet Syndrome.
Epilepsy Blog Relay: Clair and daughter Riley give tips on epilepsy first aid
Five yr. old Riley has an amazing understanding of epilepsy and epilepsy first aid. Don’t miss this video where Riley explains epilepsy first aid. Claire has shared her top 5 tips for explaining epilepsy with kids.
Epilepsy Blog Relay: Dana is loving life as an epilepsy mom
I never expected to be on this journey as an Epilepsy Mom but here I am.