Every July, we observe National Cleft & Craniofacial Awareness and Prevention Month—a time to shine a light on conditions that affect thousands of children and families across the country.
With that in mind, we are sharing helpful information to support the individuals and families navigating the challenges of cleft lip, cleft palate and other conditions every day.
Key Takeaways:
What Are Cleft and Craniofacial Conditions?
These are birth conditions that affect the structure of the head and face. The most common include:
These conditions can impact a child’s ability to eat, speak, hear, and breathe, and often require long-term care.
Who Is Affected?
Cleft lip and cleft palate affect thousands of newborns and their families each year. Here are some key stats to be aware of:
How to Reduce the Risk
Clefts form early in pregnancy and are believed to be caused by a mix of genetic and environmental factors. While not all cases are preventable, parents can reduce risk by:
Treatment options for craniofacial differences
Cleft Care Costs and Insurance Tips
Cleft and craniofacial care can be expensive. For example:
Most employer-based and military (Tricare) insurance plans cover cleft care, but families may still face copays or limits on services like speech therapy or orthodontics. Always check with your provider and care team to understand what’s covered and what documentation is needed.
Where to Find Help for Cleft and Craniofacial Care
Support is available is available for cleft and craniofacial conditions. Many hospitals offer financial assistance, especially those funded through the Hill-Burton Act. There are also organizations that provide year-round support, education, and advocacy for families, including:
Why Awareness Matters
National Cleft & Craniofacial Awareness and Prevention Month is more than just a time to share facts—it’s a chance to uplift families, celebrate progress, and advocate for better care and understanding. Whether you're a parent, provider, or supporter, your voice matters. By spreading awareness, supporting early treatment, and connecting families with resources, we can help ensure that every child born with a cleft or craniofacial condition can thrive.
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