Mission and Vision


Our Mission

To improve the quality of life for individuals with Cardio Facio Cutaneous Syndrome and their families through support, research, awareness and education.

Our Vision

To advance understanding and treatment of CFC syndrome.

Our core methods:

  • To provide support as needed by people affected by CFC syndrome through outreach, education and information sharing.

  • To ensure that physicians have ready access to the latest information to enable accurate diagnosis and proper symptom treatment.

  • To maintain and expand a registry of individuals with CFC syndrome.

  • To foster and facilitate medical research on CFC syndrome including development of appropriate treatments.

  • To maintain and grow a broad base of funds needed to expand our mission and goals.

  • To provide sustainability of the organization through continuity and growth.

  • To support a collaborative relationship among the conditions of the RAS pathway.

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