Arlo Dennis is a local 2.5 year old who has suffered seizures since birth. After extensive testing it was found that Arlo has a rare genetic mutation called STXBP1. It is estimated that only 1 in 91,000 children are affected by this mutation. It's symptoms include seizures, developmental delay, intellectual disabilities, hypotonia, among others. Arlo has a lifetime of challenges ahead. As of now, Arlo has uncontrollable epilepsy and developmental delay but thanks to 5 hours of weekly therapy and numerous specialists at CHOP and A.I. duPont as well as chiropractic care, he is making slow but steady progress. Arlo's medical challenges come with continuing expenses and needs for special equipment and have become a financial burden for his family. Help support Arlo and his family on their journey.