Counseling and Support
All caregivers want their children to develop a positive self-image, to have the same opportunities as other children, and to mature into well-adjusted, productive adults. Caregivers of children with cleft lip and/or palate share these same hopes and dreams, but they often wonder whether their child's cleft may keep them from reaching these goals. It is essential that these children receive support from their families, friends, and trained providers as needed, to ensure that their self-esteem and confidence develop as they should. It is also important for caregivers to have a community of support as they bring their children through medical appointments and treatments.
Around the world there are groups dedicated to supporting children and their families affected by cleft lip and palate. Some are led by specialists and specific organizations, while others are spearheaded by families affected by clefts themselves. Some offer in-person activities such as cleft camps, while others are focused on online communication such as closed Facebook groups. They each have their own personality and strengths, so it is important for families to explore options to see which is best for their needs.
In addition to these resources, support can be found through CLEFTLINE, a toll-free number for information about cleft lip and/or palate. They can be reached at 1-800-24-CLEFT (1-800-242-5338) or 919-933-9044.
Caregiver and Family Resources
RESOURCES FOR THOSE AFFECTED BY CLEFT
DISCLAIMER: The information provided here is meant to be helpful to you for informational purposes only. The information contained here should not be used as a substitute for medical advice. Please consult a medical professional with any questions you might have. Although we attempt to provide accurate and up-to-date information, we make no guarantee to that effect and are not responsible for the content of these resources.