About LGS
- Like many rare conditions, Lennox-Gastaut Syndrome can be a complete mystery when you first hear about it. Explore this section to get a thorough understanding of LGS—including its causes, symptoms, diagnosis and treatment.
New to LGS
- A diagnosis of LGS is deeply unsettling and can leave you at a loss as to where to turn for help and guidance. We’re here for you. In this section you will find information, resources, and communities of support for the challenging road ahead.
For Families
- If a loved one is living with LGS, the entire family shares in the difficult journey. How can you keep them safe? Find appropriate medical care? Get the support you need? This section gives answers to these and other critical questions.
About Research
- Even as our understanding of LGS grows, there is so much more to learn. From research grants to conferences, from publications to voice of the patient family, this section provides avenues for furthering your knowledge and impact.
Get Involved
- Host a fundraiser. Volunteer at an event. Shop our LGS store. These are just some of the ways you can lend your personal support to our mission. Check out this section to get started.
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Home / Team / Deena Andreola

Deena Andreola

Board Member

Deena Andreola is a Director of Advocacy in the pharmaceutical industry. She strives to forge collaborative relationships with patient organizations, elevate the voices of patients and caregivers, and foster community connections with her internal colleagues. Before this, Deena spent several years working in pharmaceutical sales within the neuroscience space. Deena began her career in direct patient support, working as a mental health worker and case manager.

Deena lives in New Jersey with her husband, Tom, their two children, Dominick and Julianna, and their fabulous pets, Buddy the dog and Taoski the cat. In her free time, she enjoys reading, cooking, spending time outdoors, and attending Broadway shows.

Learn More About Our Board of Directors here.