ENHANCING THE QUALITY OF LIFE FOR RARE AND UNDIAGNOSED CHILDREN IN TEXAS

TEAMS

Child gets placed on their dream team as an 

honorary teammate 

MENTORS

Children participate in mentor relationships 

and inspirational events 

WELLNESS

Children & families get access to mental health 

& wellness programs

ASSISTANCE

Families get financial assistance for medical 

& other expenses

A CC4C CHILD'S JOURNEY

7.6 Years

Of Testing

8-12 

Physicians

Misdiagnoses

2-3

Americans with Rare Diseases

30 Million

Genetic

80%

Are Children

Most

An Incoming

Child Often Feels

  • Socially Isolated

  • Depressed

  • Hopeless

An Outgoing

Child Often Feels

  • Supported

  • Joy

  • Hope

WAYS TO GET INVOLVED

Donate Airline Miles

One-time or Monthly Donation

Become a VIP Advocate 

 CC4C Child Spotlight 

 Hi, My Name is Sophia 

I was born in 2010 and have been diagnosed with chromosome duplication 1Q21.1

At 6 months old, Sophia’s pediatrician had a feeling that she may have a genetic disorder, based on her facial features. He referred us to a genetic doctor as well as a cardiologist, due to the sound of her heart. Sophia was diagnosed with an extra valve on her heart as well as a very rare chromosome duplication 1Q21.1. No medical knowledge of her chromosome duplication exists. Sophia is currently in two different studies on her specific duplication and is the lead patient for their medical research.

One year later when she was 16 months old, she had surgery to correct the valve on her heart. Less than 6 weeks later our lives changed dramatically. Sophia went completely non-verbal and was experiencing severe migraines that caused her to be on a liquid diet for the next 2 1⁄2 years. Within 4 weeks we would begin our journey.

From January 2012 to December 2012 we had a team of 12 doctors monitoring and giving us a list of diagnosis. Chiari Malformation, Cranial Stenosis, severe sleep apnea, failure to thrive. On December 12, 2012 she had an extensive surgery on her head and neck to relieve pressure on her brain and neck.

Sophia has a “multiple complicated medical diagnosis”, a combination of 8 as of today. Sophia has the most beautiful outlook on life. She loves people, nature, and animals. She would love to ride a horse one day. She is so expressive in how she describes beauty. I tell people all the time, “Everyone needs a Sophia in their car.”

Read More 

JOIN OUR CC4C COMMUNITY

INSPIRED... BE INSPIRED

You can be a part of the community that is bringing inspiration to children, families and others in Texas and around the world. Through our monthly giving program, 100% of your recurring gift will go towards the children that we serve!

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11701 Bee Caves Rd Suite 200
Austin, TX 78738

info@cc4c.org

512-777-1065

CONTACT US

THANK YOU SPONSORS

MISSION

To enhance the quality of life for children with rare & undiagnosed conditions. 

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CC4C is a 501c3 nonprofit foundation. Tax ID 45-3772547