The AGS Awareness Organization is dedicated to increasing public knowledge of Aicardi-Goutières Syndrome (AGS) while fundraising for research to develop novel treatments and a cure. Our mission is to improve the quality of life for those affected by this rare genetic disorder.
Headquarters:
United States of America
Company Type:
SME
Company size:
1-10 Employees
Year Founded:
2020 (6 years)
Address:
ATLANTA, US
LOW
spending power
