You are invited to join the Congenital Heart Public Health Consortium (CHPHC). The CHPHC represents various individuals and organizations across federal, state and local communities. Members represent the voice of providers, patents, families, clinicians and researchers. The CHPHC was formed in an effort to utilize public health principles to affect change for those whose lives are impacted by Congenital Heart Defects (CHD).

The mission of the Congenital Heart Public Health Consortium is to prevent congenital heart defects and improve outcomes for affected children and adults. The Consortium achieves its mission by:

  • Providing leadership and a unified voice for public health priorities
  • Expanding opportunities for surveillance and public health research
  • Informing public policy priorities that benefit public health and affected persons

CHPHC members have access to reliable information through regular members only communication as well as via online informational sessions. As needed, individuals are able to volunteer their time, talent and expertise through participation in consortium workgroups and committees. Most of all members join to participate and add their voice to awareness building activities that enhance the public health outcomes for persons living with CHD.

Are you interested in learning more about the CHPHC and its activities? Would you like to become a more active member of the CHD community? If so, please fill out the form below.

The Congenital Health Public Health Consortium (CHPHC); it is supported by the Centers for Disease Control and Prevention of the U.S. Department of Health and Human Services (HHS). The outputs of the CHPHC are solely the responsibility of the CHPHC and do not necessarily represent the official views of, nor an endorsement by the member organizations of the CHPHC, CDC/HHS, or the U.S. Government. 

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