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 / Tayla Shoultz

Tayla Shoultz

Central Region

Tayla Shoultz lives in southern Indiana with her son Brian and their 2 dogs. Brian is a wind-n-crazy full of life 17 year old, who loves girls, dogs, and playing outside. Brian does not let the daily seizures hold him back. Tayla met Brian while she was teaching, and she has since taken on a less stressful career to provide the flexibility and level of care that Brian needs. The thing she missed the most about leaving the classroom beside her students, was helping families have their needs met and having someone who understands their daily struggles. Tayla became involved with the LGS Foundation shortly after meeting Brian and had used the support group and meeting with local families to fulfill her desire to help others.