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The STXBP1 Foundation supports families affected by STXBP1-related disorder while advancing research toward better treatments and a cure. Created by parents, the organisation connects families, clinicians, scientists, and other partners around a rare neurodevelopmental condition often associated with epilepsy. Its work includes educational resources, research funding, advocacy, family connections, and opportunities to participate in studies. By bringing lived experience into scientific collaboration, the foundation helps researchers understand needs that matter to patients and caregivers. Donations sustain both community support and research progress, giving families information and relationships today while investing in discoveries that may improve care in the future.
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