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Official Merchandise

Official Merchandise

We Are STXBP1 Strong

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We Are STXBP1 Strong, a Black Crewneck Sweatshirt
We Are STXBP1 Strong, a Black Crewneck Sweatshirt (back-view)

Crewneck Sweatshirt

$36.99
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We Are STXBP1 Strong, a Solid Black Blend Premium Long Sleeve Tee
We Are STXBP1 Strong, a Solid Black Blend Premium Long Sleeve Tee (back-view)

Premium Long Sleeve Tee

$31.99
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We Are STXBP1 Strong, a Solid Black Blend Premium Unisex Tee
We Are STXBP1 Strong, a Solid Black Blend Premium Unisex Tee (back-view)

Premium Unisex Tee

$27.99
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We Are STXBP1 Strong, a Black Pullover Hoodie
We Are STXBP1 Strong, a Black Pullover Hoodie (back-view)

Pullover Hoodie

$38.99
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We Are STXBP1 Strong, a Space Black Allmade Eco Triblend Long Sleeve Tee
We Are STXBP1 Strong, a Space Black Allmade Eco Triblend Long Sleeve Tee (back-view)

Allmade Eco Triblend Long Sleeve Tee

$33.99
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We Are STXBP1 Strong, a Black Youth Long Sleeve Tee
We Are STXBP1 Strong, a Black Youth Long Sleeve Tee (back-view)

Youth Long Sleeve Tee

$24.99
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We Are STXBP1 Strong, a Black Softstyle Youth Pullover Hoodie
We Are STXBP1 Strong, a Black Softstyle Youth Pullover Hoodie (back-view)

Youth Softstyle Pullover Hoodie

$33.99
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We Are STXBP1 Strong, a Black Youth Unisex Tee
We Are STXBP1 Strong, a Black Youth Unisex Tee (back-view)

Youth Unisex Tee

$22.99
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We Are STXBP1 Strong, a Dark Grey Heather Premium Youth Tee
We Are STXBP1 Strong, a Dark Grey Heather Premium Youth Tee (back-view)

Premium Youth Tee

$23.99

Our Mission

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STXBP1 Foundation is a 501(c)3 dedicated to raising awareness and finding a cure for STXBP1 Encephalopathy, a rare neurodevelopmental condition and genetic epilepsy. We work with families, physicians, scientists, and pharmaceutical innovators. The STXBP1 Foundation was created by a group of dedicated parents. Our Non-Profit is focused on advocacy, driving research, and providing our families and their physicians with information and resources.

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STXBP1 Foundation
Verified Nonprofit
About
Non-profit dedicated to ending STXBP1 Disorders and educating others about this rare disease.