Community Advocates

In order to stay up to date on latest treatments, drug discovery, clinical studies and how to cope with epilepsy disease every day, brings you frequent articles, points of view and advice from leading patient advocates and experts.

Current advocates

Hailey Adkisson

Hailey Adkisson is a community college professor, a stereotypical Oregonian, a wife, a mother of three, and in her "free time", an unofficial PT, OT, SLP, nurse, and pharmacist to her daughter, Juniper, who has intractable epilepsy.
Read more.

Gabrielle Foote

Gabrielle Foote is 33 years old, stay at home mom who is attending ASU for Biomedical Sciences. She has a supportive husband of four years and a 1-year-old daughter. Gabrielle was officially diagnosed with Epilepsy at age 16. However, it is believed she has had epilepsy her entire life. Read more.

Lorrie Forseth

Hi, my name is Lorrie, I am from Vancouver BC, Canada & I am a proud mom of 2 daughters. I am a post-secondary Early Child Education Assistant (also known as ECE-a). I am a sports fan of Canucks hockey, Vancouver Canadians baseball and BC lions’ football, I enjoy stuff like baking shows, talk shows & so much more. Read more.

Derra Howard

My battle with epilepsy began at 9 years old, I remember being at school. I was going to the snack line and it was like I was walking into a black tunnel. The next thing I remember is being in the hospital. Read more.

Stacia Kalinoski

Stacia Kalinoski’s first seizure surprised everyone. She was a healthy college runner, preparing for her junior cross country season at the University of Minnesota in 2005 when she had a seizure at her apartment. Read more.

Kathleen Lear

I am a stay-at-home mom to Matthew, born November 2002, diagnosed with intractable epilepsy in October 2008, who is currently treated by epileptologists at Children’s Hospital Orange County (CHOC), and Andrew, who was born February 2004 and is neurotypical. Read more.

Miles Levin

Miles Levin is an award-winning filmmaker, epilepsy advocate, and Board Member at Epilepsy Foundation of Northern California. He has lived with intractable epilepsy since age 4 and is passionate about awareness. Read more.

Anita Meeks

Anita Meeks was first diagnosed with Epilepsy at the age of 50. At the same time, even a bigger shocker came being told that she has had Epilepsy the majority of her life, possibly well into the early years of childhood. She is a single mother to two boys, ages 30 and 14. After this diagnosis, Anita’s life forever changed. Read more.

Megan Mejia

I've had epilepsy since 2013. I've failed 5 medications and had a VNS implant to try to control my seizures. I'm currently having between 4-7 seizures a week and am waiting for my medical alert service dog due to come home in February 2022. Read more.

Nisshaa Muniandy

Nisshaa was diagnosed with epilepsy when she was six and dystonia at 17. Nisshaa had dystonia when she was six years old but her doctors failed to identify at a young age. Dystonia is rare in Malaysia and it’s new to some doctors. Dystonia is a movement disorder that causes involuntary muscle contractions, while epilepsy is a neurological disorder in which brain activity becomes abnormal, causing seizures, among others. Read more.

Whitney Petit

Whitney Petit is an Epilepsy Blogger, Patient Leader & Advocate who shares her lifelong journey with epilepsy through her blog Changing Focus. Whitney was first diagnosed in 1986 at 3 weeks old and currently lives with Temporal Lobe Epilepsy. She works with patients to help them understand and take control of their lives with epilepsy, and companies to show that patients are more than their diagnosis.
Read more.

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