We need your help
Families of children and adults with AGS have the odds stacked against them. Since AGS is incredibly rare and has no government funding, the responsibility is on families to find a cure for our loved ones.
We need YOU to help make this happen. All of our members are always willing to discuss and help facilitate ideas that will result in raising awareness and/or funds for AGS research. Contact info@agsaa.org.
The AGSAA is a 501c3 nonprofit foundation (tax ID 81-2738041).
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