Our Mission
To enhance the quality of life for rare/undiagnosed children.
To enhance the quality of life for rare/undiagnosed children.
Any child, anywhere, without answers to their illness, will have a community to turn to for resources and support to heal.
We enhance the quality of life for rare/undiagnosed children by building support teams for them and their families.
In 2006 my daughter, Cheyanna, was very sick and not a single specialist could diagnose her disorder. The fear of the unknown made me want to run away. Instead of running away, I just ran and ran and I kept running for an answer for my Cheyanna. During the time she was undiagnosed, I felt isolated, desperate and afraid, yet there was no community support for us. Not a single doctor, family member or friend could understand our situation. Eventually, when we did find an answer, it was a RARE condition without a treatment or a cure. However, we continued to seek therapies and treatments and received a miracle healing. Because she was healed, I felt compelled to start CC4C in 2012 in hopes more children with undiagnosed or rare conditions would have opportunity to heal. There are countless children like Cheyanna who need a Champion to fight for them. CC4C keeps these children emotionally uplifted, so they have the physical fight to continue while we support them to physical wellness. Together we can Champion these children and their families out of the darkness of isolation and into the light of love, hope and community support.
Talaya Frazier, founder