Cystic Fibrosis Foundation
CFF is the world’s leader in the search for a cure for cystic fibrosis. Find information about CF, including treatment and research and how you can get involved.
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Showing 1 - 8 of 8 results
Cystic Fibrosis My Way: Managing Daily CF Care
In this series of videos, cystic fibrosis patients from The Children's Hospital of Philadelphia show how to properly perform some common CF therapies at home.
CureHHT
Cure HHT has consistently been at the center of the national and global effort to advocate for patients and families, raise awareness of HHT, guide and fund critical research, create lasting collaborations and encourage scientists to work on new treatments.
HHT Guidelines
From the Annals of Internal Medicine, the Second International Guidelines for the Diagnosis and Management of Hereditary Hemorrhagic Telangiectasia.
HHT Nosebleed Treatment Options
This resource provides a view of the many treatment options for nosebleeds cause by Pediatric Hereditary Hemorrhagic Telangiectasia (HHT).
Scholarship and Grant Programs for Cystic Fibrosis Patients
Cystic fibrosis patients should consider this list of scholarship opportunities and grants. Look for one that might be a fit for you.
Crisis Resources
View a variety of help hotlines, as well as websites available for families in need.
Virtual Cooking Classes for Children with Cystic Fibrosis and their Families
Sign up for virtual cooking classes on healthy eating for children with cystic fibrosis (CF) or watch previously recorded classes.