National Cleft and Craniofacial Awareness and Prevention Month
United States
About
National Cleft and Craniofacial Awareness and Prevention Month is observed throughout July to raise understanding of cleft and craniofacial conditions—differences affecting the structure or development of the face, head, and related features. The month highlights the experiences of children, adults, and families while recognizing the specialists, support networks, and organizations that help individuals receive comprehensive care and encouragement.
Throughout July, the observance invites communities to learn more, challenge misconceptions, and promote compassion and inclusion. It also emphasizes the value of early evaluation, ongoing medical support, and access to trusted information, while encouraging conversations about prevention when possible. By sharing knowledge and uplifting personal stories, National Cleft and Craniofacial Awareness and Prevention Month helps build a more informed and supportive world for everyone affected.
History
National Cleft and Craniofacial Awareness and Prevention Month is observed throughout July to increase public understanding of cleft lip, cleft palate, and other craniofacial conditions. These conditions include differences affecting the face, skull, jaw, and related structures, many of which are present at birth. The observance also highlights the broad range of professionals involved in care, including surgeons, pediatricians, dentists, orthodontists, speech-language pathologists, audiologists, genetic counselors, nurses, and mental-health specialists.
Its history developed from decades of advocacy by families, medical professionals, and nonprofit organizations serving people with craniofacial differences. Organizations such as the American Cleft Palate-Craniofacial Association and the Children’s Craniofacial Association helped promote coordinated treatment, family support, research, and public education. As these efforts gained wider recognition, July became associated with a national campaign encouraging people to learn about craniofacial conditions and the specialized care they may require. Rather than focusing only on surgery, the observance reflects the modern understanding that treatment can extend across childhood and adolescence and may involve speech, hearing, dental development, breathing, nutrition, and social well-being.
The prevention component has also broadened over time. Public-health messages commonly address prenatal health, access to medical care, nutrition, genetic counseling when appropriate, and the importance of folic acid during the reproductive years. Cleft and craniofacial conditions have many causes, including genetic and environmental factors, so prevention messages are presented as risk-reduction efforts rather than guarantees. This distinction is important because many families cannot identify a single cause, and individuals with craniofacial differences should not be blamed for their condition.
Culturally, National Cleft and Craniofacial Awareness and Prevention Month has helped move discussion away from stigma and toward inclusion, informed care, and respect for individual identity. Awareness efforts encourage earlier referrals, better access to multidisciplinary treatment, and support for families navigating diagnosis and long-term care. They also give people with cleft and craniofacial differences a larger public voice, emphasizing that these conditions involve much more than appearance and that successful support includes confidence, communication, education, and participation in community life.