07/10/2026
"I always had this moment of every surgery, every recovery is temporary. I know that I'm going to be able to go back to the things that I really love doing day in and day out."
For children growing up with a cleft lip and palate, it can be hard to imagine that the challenges they're facing today won't last forever.
As we continue recognizing National Cleft & Craniofacial Awareness and Prevention Month, we're honored to share the stories of the Austin Smiles community. Throughout July, you'll hear from individuals born with a cleft, parents, healthcare providers, volunteers, and advocates whose experiences highlight the power of hope, resilience, and compassionate care.
Today, Kendall Burton reflects on what it was like growing up with a cleft, shares the advice she wishes every child could hear—that the difficult moments won't last forever—and explains why she's grateful for organizations like Austin Smiles, whose life-changing care and support help children and families in Central Texas and Latin America face the future with confidence.
💙 Watch her story.
💙 Share this post to help educate others about cleft lip and palate.
💙 Help us create a more informed, compassionate world for every child and family affected by a cleft.
Every story creates understanding. Every share creates awareness. Every child deserves to know they're not alone.
