CurePDE Foundation

CurePDE.org is a patient advocacy organization that provides essential resources, education, and community support for those affected by Pyridoxine-Dependent Epilepsy (PDE), a rare genetic disorder responsive to vitamin B6. We collaborate with researchers, clinicians, and advocacy groups worldwide to support scientific discovery, enhance treatment options, and raise awareness about PDE. Our programs include patient education, family support networks, and funding initiatives to advance PDE research. By empowering patients and caregivers with information and access to the latest developments, CurePDE.org aims to create a brighter future for everyone impacted by this rare condition.