Welcome to CFFC!
The Cystic Fibrosis Family Connection (CFFC) is a charitable, not-for-profit corporation established to assist cystic fibrosis patients and their families.

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CFFC:
Dedicated to supporting CF patients and families in their daily struggle with cystic fibrosis.

Learn more about CFFC
Our Lung Transplant Story
Personal insights on the lung transplantation journey.

Read the story
Help Us Help Others
Your contributions lend a hand to the CF community through Hospital Help Packets, information sharing events, emergency grants, and more.

Support CFFC

Supporting Our Rochester/Finger Lakes CF Community

Name: BreatheCon 2020
Start: 2020-09-25T00:00:00-04:00
End: 2020-09-26T23:59:59-04:00
Location: On-line Community

CFFC is dedicated to supporting CF patients and families in their daily struggle with cystic fibrosis.

Easing the financial burden of hospitalization. Click the link above to learn more.

Hospitalizations can be a very stressful time for CF patients and their families. Click the link above for facts and tips to ease this experience.

Publications from Cystic Fibrosis Australia

Cystic Fibrosis Australia has produced a wide range of brochures Read more →
Resources for Supporting Families Coping with Chronic Illness

While cystic fibrosis presents many unique challenges, people living with Read more →
A Daughter’s Perspective on Transplant

We have added a new page to the Our Lung Read more →
A Guide for CF at School

Cystic Fibrosis Ireland has published a guide intended to help Read more →
Breathe for Bea Foundation Scholarship

The Breathe for Bea Foundation recently opened their cystic fibrosis Read more →