Our mission is to empower, support, and unite individuals affected by craniofacial anomalies through a nurturing community.
Our Founder went to a routine anatomy scan and learned that her baby (Liam) would be born with a cleft lip and other special needs. She experienced the isolation and financial strain of accessing the necessary resources and support for her child's care and survival. She founded Cleft Lip Warriors to be a beacon of hope for families facing the challenges of craniofacial anomalies.
Our team is a diverse group of passionate individuals, many of whom have had personal experiences with the challenges our families face. From our founder, a medical mom, to our volunteers, every member of our team is committed to providing unwavering advocacy for the children and families we serve.
Cleft Lip Warriors is dedicated to improving the lives of babies, children and adults who have craniofacial anomalies.
Warrior spotlight is a carousel of stories on the Cleft Lip Warriors website that discusses real life accounts of what families experienced finding out that their child and/or loved one was going to be born with cleft lip, cleft palate or both. The spotlight is a way for viewers to learn more about what could happen during a pregnancy and how families navigated through the diagnosis.
Cleft Lip Warriors will be releasing new information over the next few months about sponsorship programs where funds will go to sponsoring a family who is in financial crisis and needs assistance in paying their loved ones medical bills who have craniofacial anomalies. Medical bills could also include awake night care. For more information, please send an email to cleftlipwarriors@gmail.com
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