Living With Lennox-Gastaut Syndrome (LGS): Appreciating Every Moment Together
Rachel shares the story of her family’s efforts to find quality time despite challenges of LGS Epilepsy.
Living Well With Epilepsy’s, Epilepsy Blog Relay™ is an epilepsy awareness movement to designed to maximize collaboration and eliminate stigma. The theme is: “EPILEPSY AWARENESS: Stronger Together”
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Rachel shares the story of her family’s efforts to find quality time despite challenges of LGS Epilepsy.
Comedian and actor, Bob Dibuono, shares his family’s experience with SUDEP and New-Onset Refractory Status Epilepticus (NORSE).
Jewel shares a few tips on how to keep track of your seizures. We hope this helps as you move through your own epilepsy journey.
At #WHA73, Member States endorsed a resolution calling for global action plan on epilepsy and other neurological disorders. Learn more.
Amanda encourages readers to remember we are resilient, as we manage the pandemic, seasonal changes and a chronic condition.
For the researcher interested in developing Neurotherapeutics who is looking for ways to network with experts in academia, industry, advocacy, and government here are three great opportunities.
Lauren shares her experinence of “showing up for yourself” after her diagnosis of epilepsy.
Recently Colleen was sick and hadn’t eaten in days. Jenny shares her experience with practicing gratitude during this difficult time.