Our Mission

To enhance the quality of life for rare/undiagnosed children. 

Our Vision

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.

  • Each child is placed on a high school “Dream Team.” The team dedicates their season to bringing joy and inspiration to the child. The team makes their child an honorary teammate for the school year, providing unique opportunities for the child to feel a part of a team. In turn, the program inspires the student-athletes to be role models to younger children, and to live and train with care and concern for others.
  • Each CC4C family has funding available to them through CC4C’s Financial Assistance Program. This program helps cover medical expenses insurances deny. Expenses include homeopathic, eastern and western medical treatments/therapies as well as travel to specialists that may not otherwise occur without the financial assistance from CC4C.
  • Each CC4C Family has the opportunity to participate in our new Mental Health and Wellness Program. The Mental Health and Wellness program was created in efforts to support the CC4C children and their entire family.
  • We host inspirational events for families to create lifetime memories and unforgettable family bonding. We organize campaigns, and fundraisers to provide families a community of support through our CC4C programs, to bring awareness to the needs of this population.


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