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No Family Journeys
Rare & Undiagnosed Alone—
Guided by Hope, Faith,
Love, and Gratitude.

No Family Journeys
Rare & Undiagnosed Alone—
Guided by Hope, Faith,
Love, and Gratitude.

Welcome to CC4C

CC4C is a 501(c)(3) nonprofit organization dedicated to improving the quality of life for Texas children living with rare and undiagnosed medical conditions. Founded in 2012 by Talaya Frazier during her daughter Cheyanna’s journey, CC4C walks with families from diagnosis through long-term care—transforming isolation into community.

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Our Impact

A CC4C CHILD'S JOURNEY

An Average of

7.6 years

Of Testing
 

8-12 Physicians

2-3
Misdiagnoses

30 Million
Americans with Rare Diseases
 

80% Genetic

 

Most
Are Children

See how
we impact
these numbers!

Every year, CC4C:

  • Funds critical care—covering therapies, adaptive equipment, and travel to specialists denied by insurance.
     

  • Strengthens families—through TRIBE gatherings, sibling adventures, and well-being resources that nurture every member of the household.
     

  • Creates belonging—by matching children with Dream Teams who celebrate them as valued teammates and friends, creating a true sense of belonging.
     

  • Uplifts with joy—through adaptive adventures and events that turn medical journeys into cherished memories.

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“CC4C gave us strength when we felt alone. They reminded us we’re part of a bigger family." 

– CC4C Parent

Get Involved

Together, we can prove that rare and undiagnosed doesn’t mean alone.

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Your Gift, Their Lifeline

Join the CC4C movement and be the lifeline families are praying for. Every gift—whether one-time or monthly—removes barriers to critical care and fills homes with hope, joy, and confidence. Parents tell us that your generosity gives them strength to keep going, reminding them they are not alone. By giving, you build stability, spark joy, and create lasting impact for children and families across Texas. Choose the way that’s right for you, and know that every dollar brings love and healing closer to home—one family, one moment at a time. Discover all of the many ways you can contribute. 

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“We truly appreciate all the hard work and effort put in by the CC4C team to bring joy and happinessto our lives. The memories that we created will always hold a special place in our hearts."

– CC4C Mom

Why Our Programs Matter

Families facing rare and undiagnosed conditions often feel isolated, overwhelmed, and without answers. CC4C surrounds them with faith, hope, and community through programs that address the whole journey—removing barriers to care, nurturing emotional health, and creating lasting joy.

Financial Assistance

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Why it matters: Insurance doesn’t cover everything families need. From genetic testing to therapies and travel to distant specialists, medical costs create impossible choices for parents already stretched thin.

 

What we do: CC4C removes financial barriers by covering critical care and therapies often denied by insurance—restoring hope, stability, and gratitude in the midst of hardship.

Subscribe to our CC4C Quarterly Newsletter

Welcome to the CC4C quarterly newsletter! Your email information will be added to our database. CC4C does not sell your information to any third parties. Find us on Facebook, Instagram, Twitter, and YouTube too!

Rare Family Newsletter
Highlighting all CC4C Family Programs

The Founding Story

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CC4C began with the journey of one mother and her daughter. In 2012, Talaya Frazier founded Cheyanna’s Champions 4 Children (CC4C) after walking through the difficult and lonely path of her daughter Cheyanna’s rare diagnosis. She dreamed of creating the support and community she wished her family had—one where no parent feels isolated and every child is celebrated beyond their condition.

 

What started as one family’s need has grown into a statewide movement of hope, faith, love, and gratitude. Today, CC4C surrounds children and families across Texas with financial assistance, whole-family wellness programs, Dream Teams, and uplifting events that prove: rare and undiagnosed doesn’t mean alone.

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