Where to Find Treatment for GM1 Gangliosidosis?
Medically reviewed by David Weinstein, M.D., M.M.Sc. Where to Find Treatment for GM1 Gangliosidosis Background…
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Sweet Iris Featured on KRON 4 News: Raising Hope for GM1 on Rare Disease Day
Sweet Iris Featured on KRON 4 News: Raising Hope for GM1 on Rare Disease Day…
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Happy 18th Birthday, Sweet Iris
Happy 18th Birthday, Sweet Iris An update on Sweet Iris as she heads into adulthood,…
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Daxton’s Story
Daxton’s Story, By His Mother A GM1 Infantile (Type 1) Story(Published Feb. 20, 2026) “GM1…
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A Quickstart For GM1 Gangliosidosis
A Quickstart for GM1 Gangliosidosis What Is GM1 Gangliosidosis? GM1 gangliosidosis is a rare, inherited…
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February 2026 Cure GM1 Catalyst
As the year comes to an end, we remain focused on creating connection by keeping our rare disease community informed of advocacy opportunities, research news and community updates. Join us in learning more about our efforts to push for a cure for GM1 gangliosidosis.
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2025 Cure GM1 Impact Report
All we’ve Achieved in 2025 THANK YOU. With your help, the Cure GM1 Foundation had…
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January 2026 Cure GM1 Catalyst
As the year comes to an end, we remain focused on creating connection by keeping our rare disease community informed of advocacy opportunities, research news and community updates. Join us in learning more about our efforts to push for a cure for GM1 gangliosidosis.
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Nate’s Story
Nate’s Story, By His Mother A GM1 Late-infantile, Type 2A Story(Dec. 26, 2025) “I didn’t…