Slide We are on a Journey to find a cure. Come with us. We do not have to become heroes overnight. Just a step at a time,
meeting each thing that comes up, seeing it is not as dreadful
as it appeared, discovering we have the strength to stare it down.
Our Journey

Where it Started

Taylen, born a bright-eyed bundle of joy to William and Jenece Horton, didn’t experience any issues in the few months of life. That is until her parents noticed at about three months old, that their baby girl was having some difficulty with her arm. Taylen’s arm started to jerk unexpectedly and the infant clinched her fist tightly, which was troubling enough for her parents to take notice. Read more…

About Dravet’s Syndrome


Dravet syndrome, previously known as severe myoclonic epilepsy of infancy (SMEI), is a type of epilepsy with seizures that are often triggered by hot temperatures or fever. It is treated with anticonvulsant medications. It often begins around six months of age.


Taylen was diagnosed with Dravet Syndrome at the age of one after a painful year for her parents trying to figure out what was wrong and an abundance of tests, misdiagnoses and ill health’.


Dravet syndrome has been characterized by prolonged febrile and non-febrile seizures within the first year of a child’s life. This disease progresses to other seizure types like myoclonic and partial seizures, psychomotor delay, and ataxia. It is characterized by cognitive impairment, behavioral disorders, and motor deficits.


It affects around one in 20,000 people worldwide.


With her strong will and EVERYONE’S prayers and support, we all believe we can help Taylen and so many more children affected by Dravet Syndrome. It’s time we come together and help Taylen and her family in this time of need!! Please help in any way you can!

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