Hope for PDCD Foundation

Global Genes Global Advocacy Alliance member focused on rare disease support, education, advocacy, or research. Our mission is simple: to find a cure for PDCD. 1 in 40,000 children is born with PDCD; genetic medicine, combined with standards of care, small molecule therapy, and early diagnosis, will give them a fighting chance1. Our work will help advance research for AAV9 genetic medicine, which is currently the best hope for PDCD and other neurodegenerative diseases. Directory information only; not medical advice, legal advice, or endorsement. Services and eligibility should be confirmed with the organization.