The FamilieSCN2A Foundation

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Our vision is to find effective treatments and a cure for SCN2A disorders. Our vision is a world with effective treatments and cures for ALL SCN2A-related disorders. "Families" is part of our name for a reason. Rare and devastating, SCN2A-related disorders affect the entire family. Our team of leaders strive every day and in every way to improve the lives of not only the patients, but the entire family. Our MISSION is to accelerate research, build community and advocate to improve the lives of those affected by SCN2A-related disorders around the world. Our VISION is a world with effective treatments and cures for all SCN2A-related disorders. Our Values are URGENCY, INTEGRITY, COLLABORATION, and INCLUSION.

Founded

2015

Facebook

6300

X (Twitter)

1599

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4412245

Address: PO Box 4260, GettysburgWeb: Sign in to see organisation websiteFacebook: FamilieSCN2aFoundationX (Twitter): familiescn2aEmployees: 3Volunteers: 20Revenue: 1860699ICO: 473169795

FamilieSCN2A Foundation The SCN2A gene is located on the long q arm of chromosome 2 at position 24. 3. SCN2A encodes instructions to make a protein in the brain called a sodium channel which plays a key role in a cells ability to generate and transmit electrical signals. Pathogenic variants that affect the SCN2A sodium channel impair the flow of sodium ions in the brain.

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The FamilieSCN2A Foundation

3 Days to Go 💙💜💚 “This is for Griffyn-and for every Warrior still fighting in silence. " Not attending a Warrior Challenge in person. You can still make a difference from afar.

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Janet

This foundation is doing such important work! Together, we can support families and advocate for a brighter future for those affected by SCN2A-related disorders. 💪❤️ #FamilieSCN2A

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The FamilieSCN2A Foundation

Today is SUDEP Action Day. 💜 More than 1 in 1,000 people with epilepsy die each year from SUDEP (Sudden Unexpected Death in Epilepsy) — the leading cause of death among those with uncontrolled seizures. Awareness saves lives.

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Stacy

1. What strategies can the FamilieSCN2A Foundation implement to raise awareness about the importance of genetic research in understanding and treating SCN2A-related disorders?

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Paul

2. How can we collaborate with other organizations and researchers to accelerate the development of effective treatments for individuals affected by SCN2A-related conditions?

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Michelle

Every step towards understanding SCN2A disorders is a step towards hope for families! Let’s stand together and push for more research and awareness! 🌟 #CureSCN2A

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