CC4C is a 501c3 non-profit organization dedicated to enhancing the quality of life for rare/undiagnosed children. CC4C stands for Cheyanna’s Champions for Children. Cheyanna suffered from a rare disorder and is CC4C Founder, Talaya Frazier’s daughter.

We match each Champion Child with a “dream team," composed of businesses or high school teams, who dedicate their season to the child. We also provide financial assistance to help pay for medical expenses insurance may not cover or deny. We hold inspirational fundraising events for the children, host events for CC4C parents, siblings and families that promote Family Well-Being, as well as offer resources for our Rare network.

CC4C has a large and growing community. CC4C programs reach more than 100+ children and continues to increase. Our reach includes children in over 43 cities across the state of Texas.

CC4C focuses on building a strong interactive community around each child in the Austin and surrounding areas. However, CC4C helps children all over the state of Texas. The purpose of the organization is to inspire each child to believe in their future and hope for what good tomorrow will bring. Our intention is to implement chapters in other cities once we are certain we can reproduce the community support for the children.

All families who are looking for help must apply through our website or call us directly as well as meet eligibility requirements. Application submissions are available online from Aug. 1st – July 31st each year. CC4C also helps other non-CC4C children with rare/undiagnosed conditions by providing grants throughout the state of Texas through our Statewide Medical Financial Assistance (SMFA) program.

All funds are determined by our annual budget approved by our board of directors. Each family is offered the same financial assistance opportunities. We also provide the families with benefits that aren’t attributed to costs, such as donated counseling, events and support through our different programs.

Please visit our website CC4C.org, call 512.777.1065 or email info@cc4c.org

Your primary care physician should be able identify your child’s condition. The National Organization for Rare Diseases website offers a search engine for rare diseases.

A certified physician must verify your child is undiagnosed and medically complex.

Yes, more than one child in a family can be a part of CC4C, but there are guidelines that must be followed for families with multiple children suffering from rare or undiagnosed diseases. Call 512.777.1065 or email info@cc4c.org for more information.

Visit us at cc4c.org, call 512.777.1065 or email info@cc4c.org for more information on how to volunteer.

You may check with your employers HR department or check on match capable businesses

Government assistance does not exclude your family from being a part of CC4C. Please apply online at CC4C.org for your child to be a part of CC4C.

The application forms for CC4C are located on our Financial Assistance page here: https://www.cc4c.org/financial-assistance