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Connorman developed epilepsy in 2010, 5 months after birth. It changed our lives and our sense of security immediately and forever. Connorman has never had full seizure control, but with the help of medications, a fantastic neurologist at UVA, and the support of groups like the Epilepsy Foundation of Virginia we are not just surviving, but thriving!

Help us raise funds for the EFVA to support those who need prescriptions, advice, legal council and other resources that an organization like EFVA can provide! As always, GO TEAM CONNORMAN!

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