Cystic Fibrosis is a genetic disease that mainly impacts the lung and digestive system. Those affected produce thick sticky mucus that can clog the lungs, stomach, intestines, liver, pancreas, and reproductive organs.
- Cystic Fibrosis Canada
My Health Alberta
My Health Alberta has detailed peer reviewed information that you can access by searching Cystic Fibrosis.
About Kids Health
This overview from the Sick Kids Hospital provides the basic information you should know about CF.
- Kids Health
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This all-encompassing guide provides practical advice for managing cystic fibrosis.
Cline and Greene have created this guide to help parents through the struggles of raising a child with a chronic condition.
Written for teens with input from real teens this book mixes research and personal experience to give teens all the information they need and more to manage a life with CF.
In her memoir, Cariou shares the experiences she had growing up with her sister, who had cystic fibrosis.
Twins Isabel and Anabel were both diagnosed with cystic fibrosis. Their story and the impact on themselves and loved ones is portrayed in this book.
Frank Deford shares his daughter Alex's story of cystic fibrosis from a father's perspective.
Lux gives readers an inside look at what life is like with cystic fibrosis.
Kory is a normal kid who loves to do kid things. He also has cystic fibrosis - but he knows how to take care of himself and have fun every day!
Written for pre-school aged children, Cadberry's Letters introduces children to life with cystic fibrosis.
Thank you to our friends from the Pediatric Cystic Fibrosis Clinic at the Alberta Children's Hospital.
This material is designed for information purposes only. It should not be used in place of medical advice, instruction and/or treatment. If you have specific questions, please contact your doctor or appropriate health care professional.
For more information contact the Child Health Information Specialist at 403-955-7745 or firstname.lastname@example.org