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Lafora Body Disease Day ’24 English

October 1, 2024/by Christine Kelly

#LaforaBodyDiseaseDay Fight Lafora #FightLafora Help us reach a cure!

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https://chelseashope.org/wp-content/uploads/2022/02/ChelseasHope1.png 0 0 Christine Kelly https://chelseashope.org/wp-content/uploads/2022/02/ChelseasHope1.png Christine Kelly2024-10-01 20:25:242024-10-01 20:25:47Lafora Body Disease Day ’24 English

About Chelsea’s Hope

Chelsea’s Hope began as a website in the fall of 2007 to share Chelsea Gerber’s story with family and friends. A 501(c)(3) organization since 2009, we have made an impact by raising awareness, connecting families worldwide, funding research, and maintaining hope. Our mission is to improve the lives of those affected by Lafora disease and help accelerate the development of treatments. [Read More]

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  • Chelsea’s Hope Earns Platinum Seal of Transparency for 2025

  • Chelsea’s Hope Welcomes 2025-2026 Board of Directors

  • In Memory of Dr. Joan Guinovart

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The mission of Chelsea’s Hope is to improve the lives of those affected by Lafora Disease and help accelerate the development of treatments.

Chelsea’s Hope Lafora Children Research Fund is an IRS 501(c)3 non-profit organization. EIN: 27-1008382

Location imageChelsea’s Hope, Post Office Box 348626, Sacramento, CA 95834

info@chelseashope.org

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