Cure GM1 Foundation
Awareness -> Funding -> Hope The only 501(c)(3) entirely dedicated to GM1, Founded by families impacted by GM1 gangliosidosis, a fatal disease that primarily impacts children. The Cure GM1 Foundation is dedicated to hope and to directly funding research for a cure or treatment for GM1 gangliosidosis/GM1-gangliosidosis, a lysosomal storage disease that attacks the brain and spinal cord and is always fatal in children. GM1 is a progressive and degenerative condition with an extremely broad and debilitating array of symptoms and complications. This nonprofit organization was founded by parents of children who suffer from GM1 who seek to save the lives of all those who suffer from this wretched condition. Cure GM1 is in contact with the largest number of families impacted by GM1 of any advocacy group globally.
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2014
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Brain Disorders Category
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19. THE JORDAN ELIZABETH HARRIS FOUNDATION
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Awareness -> Funding -> Hope The only 501(c)(3) entirely dedicated to GM1, Founded by families impacted by GM1 gangliosidosis, a fatal disease that primarily impacts children.
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Awareness -> Funding -> Hope The only 501(c)(3) entirely dedicated to GM1, Founded by families impacted by GM1 gangliosidosis, a fatal disease that primarily impacts children.
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Awareness -> Funding -> Hope The only 501(c)(3) entirely dedicated to GM1, Founded by families impacted by GM1 gangliosidosis, a fatal disease that primarily impacts children.
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The SMDM works with patients, clinicians, policy makers and the public to improve medical decisions.
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For more information, visit our website: www.
Awareness -> Funding -> Hope The only 501(c)(3) entirely dedicated to GM1, Founded by families impacted by GM1 gangliosidosis, a fatal disease that primarily impacts children.
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Join us and make a difference for the future!
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