Cure GM1 Foundation

Cure GM1 Foundation

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The Cure GM1 Foundation is dedicated to directly funding research for a cure for GM1 Gangliosidosis.

Photos from Armand's Hope's post 07/16/2026

Remembering Armand

Photos from Cure GM1 Foundation's post 07/13/2026

“I was preparing myself to receive bad news, but my lack of awareness on metabolic conditions kept me hopeful that I would see her grow up, possibly with few limitations."
READ: .curegm1.org/batuls-story

07/10/2026

Warning sign of GM1 gangliosidosis: clumsiness.
Children may tumble off chairs or trip when there is no obvious reason, even on flat surfaces. Frequent, unexplained falls can be one of the earliest signals of underlying neurological change in GM1.
Citation: Brigerom A, et al. GM1 gangliosidosis: the caregivers’ assessments of symptom impact and most important symptoms to treat. American Journal of Medical Genetics Part A, 2023.
Learn more: curegm1.org/about-gm1

07/09/2026

There are so many ways to Do It For GM1. Move, bake, bike, swim, dine, or build a fundraiser around something you love. Every action helps raise awareness and support research for possible treatments for this devastating and fatal disease.

https://www.curegm1.org/do-it-for-gm1/

07/08/2026

Build water into the day, every day.

Children with GM1 often cannot ask for a drink. Hydration cannot wait for thirst.

For tube-fed kiddos, talk with your care team about adjusting free-water flushes in the heat.

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PO Box 6890
Albany, CA
94706