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Epilepsy Blog Relay™: Megan’s Story

Day 19 of the Epilepsy Blog Relay™

Today’s post comes from Megan Davis who writes In Megan’s Shoes, which is an honest and personal look at this young wife and mother’s epilepsy. One reader commented recently on a recent post, “Thank you for letting us in!”

 

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Jessica K. Smith Founder and CEO; Executive Director
Jessica Keenan Smith is a patient advocate and epilepsy community leader with more than 15 years of experience. As Founder and CEO of Living Well With Epilepsy and Executive Director of ASENT she bridges the gap between the scientific and patient communities, with a particular focus on the needs of the epilepsies. Jessica Keenan Smith is Founder and CEO of Living Well With Epilepsy, an award winning online resource for people affected by epilepsy to share stories and access in-depth information on the disease. Since 2009, Living Well With Epilepsy (https://livingwellwithepilepsy.com) has been featured in Forbes, Wired, NBC, NPR and the cover story of Epilepsy Advocate Magazine and has partnered with companies such as UCB, Lundbeck, Sunovion, Eisai, and more. Ms. Smith is also the Executive Director of the American Society for Experimental Neurotherapeutics (ASENT) (https://asent.org), an organization that brings together leaders from industry, academia, government and advocacy who are engaged in bringing drugs and devices to market across all neurologic disease states. In this role she is responsible for leading a successful scientific journal and annual scientific conference with speakers from all over the world.

  1. Beverly Partain
    | Reply

    My daughter was diagnosed with epilepsy at age 14. She’s had about 9 grand-mal seizures , some peti- mals and one I have no name for. I am frantic every time she drives. I worry when she leaves the house. She starts off with the peti-mals then the grand-mal seizure happens. I pray for a cure. She’s 19 now and wants to go to college and be normal like her friends

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