When my daughter Avery joined the youth cheer team this year, I wasn’t sure what to expect. Because of her developmental disability, speech delay, and the many seizure triggers brought on by Dravet syndrome, her participation in youth sports has been almost nonexistent. When we walked into the cheerleading…
Embracing Life with Dravet
— Sarah Lango
Sarah Lango is a small town girl from rural Missouri whose greatest joy is being a wife and mother to three. Her full-time gig is college and career adviser at the local high school. After her youngest daughter, Avery, was diagnosed with Dravet syndrome nearly 10 years ago, Sarah made it her mission to share their journey, both the good and bad, so other families would feel less alone.
Fourteen months, or 425 days. That’s how long my daughter was free from status and tonic-clonic seizures. For most people, that doesn’t mean anything, but for someone with Dravet syndrome, seizure freedom of that length means everything. For over a year, my 10-year-old, Avery, didn’t experience any seizure…

Note: This column describes the author’s own thoughts about various seizure medications and therapies. Not everyone will have the same response to treatment. Consult your doctor before starting or stopping a therapy. Early on, when Avery, my daughter with Dravet syndrome, started having seizures, I was scared of…
A couple years ago, I was talking with several other parents when the topic of parenting “sweet spots” came up. They all had kids similar in age to mine, with one difference: My youngest daughter, Avery, has Dravet syndrome. These parents talked about entering the season when their kids…
When my daughter began having seizures at 3 months old, I immediately went into fight mode. At that time, Avery was a perfectly healthy and typically developing baby. I thought there had to be a reason these seizures were happening, and once we figured that out, we could find…
My 10-year-old daughter had an absolute meltdown when it came time to leave a family birthday party the other day. I tried to bribe her. I got down on the floor beside her to reason with her. I reminded her that there could be consequences if she didn’t listen to…
My 10-year-old daughter, Avery, has a rare, catastrophic, and lifelong form of epilepsy called Dravet syndrome. Recently, I have expressed the difficult emotions and experiences that accompany this reality. These hard things are all true, but there is another truth, too: She makes me smile every single day. Some…
When we’re at home, Avery is just Avery. But when we enter the world, go to school, or attend organized activities where age-appropriate social interactions and behaviors are the norm, Avery becomes someone who exists outside the norm. Avery is my 10-year-old daughter who has Dravet syndrome. Because of…
School started this week for my 10-year-old daughter, Avery. In many ways, Avery is like most kids — she is social, values friendship, and wants to be accepted by her peers. But in other ways, she is very much unlike her peers. Avery has Dravet syndrome, a rare, severe,…
Earlier today, I sat on the empty bleachers at our elementary school, where my daughter was participating in a youth cheerleading camp. The rest of the parents had left, but I remained because Avery has Dravet syndrome, which means she is prone to having seizures, and I wanted…
Recent Posts
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- A caregiver’s evolving perspective on seizure-control medications
- Leaving my daughter with Dravet syndrome in the care of her teen sister
- Accepting Dravet syndrome took me from fighting reality to finding peace
- Too many questions, too few answers about my daughter’s outbursts