Cardio-Facio-Cutaneous (CFC) International

CFC International was founded as a nonprofit patient support and advocacy group in 1999. Developed in the hearts of dedicated parents more than 2 decades ago, the organization has provided support to more than 900 families, over 36 countries, and dedicated more than $150,000 USD to research. We are driven to improve the quality of life for individuals with CFC Syndrome and their families through family support, research, and education.