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Jaxson's Genetics

Jaxson's Genetics

Jaxson was officially diagnosed with infantile spasms, a form of epilepsy, at 7 weeks old. After testing, we found the root of his epilepsy stems from a rare genetic mutation in his DNA called STXBP1. When he was diagnosed there were less than 200 cases in the world. Today, there are approximately 300 patients diagnosed with this condition. We not only are walking to help find a cure to Epilepsy, we're walking to bring awareness to our community. Thank you for supporting our cause!! -Jaxson's Genetics

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1. Sherry Chapman
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