CGD Association of America

Global Genes Global Advocacy Alliance member focused on rare disease support, education, advocacy, or research. The CGD Association of America (CGDAA) was founded in 2019 to advocate for patients and X-linked female CGD carriers with Chronic Granulomatous Disease (CGD). Felicia formed the CGDAA, a Sec.501c3 non-profit organization with the mission to advocate for the CGD community by providing clear, accurate, and independent news and information about CGD, advancing CGD research, and providing webinars. Directory information only; not medical advice, legal advice, or endorsement. Services and eligibility should be confirmed with the organization.