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Cystic Fibrosis Support: Better childhoods, happier families

We support children in North Carolina living with cystic fibrosis and the families who care for them.

About Friends Fighting Cystic Fibrosis (FFCF)

Friends Fighting Cystic Fibrosis is a nonprofit organization dedicated to supporting children living with cystic fibrosis and the families who care for them.

Founded by families and friends impacted by CF, FFCF exists to help when the weight of the disease becomes too heavy, offering practical assistance, compassion, and community to families during critical moments of care.

Our Mission

Friends Fighting Cystic Fibrosis provides direct support to children in North Carolina living with cystic fibrosis and their families, helping ease the medical, financial, and daily challenges of CF.

Our Vision

A future where every child with cystic fibrosis and their family has the support and resources they need to live fully, with stability, dignity, and hope.

What is cystic fibrosis?

Cystic fibrosis (CF) is a genetic disease that primarily affects the respiratory, digestive, and reproductive systems. It is caused by mutations in the CFTR gene, which leads to the production of thick, sticky mucus that clogs the airways and makes it difficult for the body to clear infections.

Our Partners

Atrium Health Logo - Teal sans-serif type with teal icon of a tree inside a circle to left
Duke Health Logo - Blue sans-serif type with shield icon to left
UNC Healthcare Logo - Cyan and dark blue sans-serif type with stylized letter N
Photo of a father holding daughter on his shoulders

Need Support?

If your child is living with cystic fibrosis and your family needs assistance, Friends Fighting Cystic Fibrosis is here to help.

Learn more about available support, eligibility requirements, and how to connect with FFCF.

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