Learn about cystic fibrosis, a genetic disorder that affects the lungs, pancreas, and other organs, and how to treat and live with this chronic disease.
CF is a rare genetic disease found in about 30,000 people in the U.S. If you have CF or are considering testing for it, knowing about the role of genetics in CF can help you make informed decisions about your health care.
If you or your child has just been diagnosed with cystic fibrosis, or your doctor has recommended testing for CF, you may have many questions.
Diagnosing CF is a multistep process. A complete diagnostic evaluation should include a newborn screening, a sweat chloride test, a genetic or carrier test, and a clinical evaluation at a CF Foundation-accredited care center.
Raising a child with cystic fibrosis can bring up many questions because CF affects many aspects of your child’s life. Here you’ll find resources to help you manage your child’s daily needs and find the best possible CF care.
Living with cystic fibrosis comes with many challenges, including medical, social, and financial. By learning more about how you can manage your disease every day, you can ultimately help find a balance between your busy lifestyle and your CF care.
People with CF are living longer, healthier lives than ever before. As an adult with CF, you may reach key milestones you might not have considered. Planning for these life events requires careful thought as you make decisions that may impact your life.
People with cystic fibrosis are living longer and more fulfilling lives, thanks in part to specialized CF care and a range of treatment options.
Cystic Fibrosis Foundation-accredited care centers provide expert care and specialized disease management to people living with cystic fibrosis.
We provide funding for and accredit more than 120 care centers and 53 affiliate programs nationwide. The high quality of specialized care available throughout the care center network has led to the improved length and quality of life for people with CF.
The Cystic Fibrosis Foundation provides standard care guidelines based on the latest research, medical evidence, and consultation with experts on best practices.
As a clinician, you’re critical in helping people with CF maintain their quality of life. We’re committed to helping you partner with patients and their families by providing resources you can use to improve and continue to provide high-quality care.
As part of the Cystic Fibrosis Foundation's mission to help improve the lives of people living with cystic fibrosis, the PSDC initiative taps the CF community to inform key efforts to support the management of daily care.
Your cystic fibrosis care team includes a group of CF health care professionals who partner with you to provide specialized, comprehensive CF care.
Many people living with cystic fibrosis and their families face complicated issues related to getting the care they need. Cystic Fibrosis Foundation Compass makes sure that no one has to do it alone.
CF Foundation Compass is a service that helps people with CF and their families with navigating insurance options, connecting to legal information and experts, finding available financial resources, and tackling other life issues.
CF care team members are paramount in providing highly specialized care to people living with CF. CF Foundation Compass can help by serving as a strategic ally for care teams, so team members can focus on their patients’ care.
CF Foundation Compass can help you navigate insurance, financial, legal, and other issues you are facing. Use this online form to start your conversation with a Compass case manager today.
The Cystic Fibrosis Foundation is the world’s leader in the search for a cure for CF and supports a broad range of research initiatives to tackle the disease from all angles.
The CF Foundation offers a number of resources for learning about clinical trials and treatments that are being developed to improve the treatment of cystic fibrosis.
Our understanding of CF continues to evolve as scientists study what causes the disease and how it affects the body. These insights drive the development of new and better treatments and bring us one step closer to a cure.
Researchers, supported by the CF Foundation, have made tremendous advances to improve the health and quality of life of people with CF. We are committed to providing the tools and resources you need to continuously build upon this work.
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Columbus' Brewers Ball Virtual Event
August 19, 2021
The Central Ohio Chapter of the Cystic Fibrosis Foundation is excited to begin accepting applications for our 2021 Columbus' Finest Professionals Campaign. Each year the CF Foundation honors a select group of men and women from around Central Ohio, who are committed to professional growth through a guided fundraising and awareness campaign.
Cleveland/Akron CF Cycle for Life - Virtual
August 21, 2021
Northern Ohio - Cleveland
CF Cycle for Life is a premier cycling series featuring bicycle rides across the country. These daylong events showcase scenic routes and multiple distances to raise funds and awareness for cystic fibrosis. Put your wheels in motion and help us get one step closer to making CF stand for Cure Found.
Central NY Xtreme Hike - Virtual
5:00 AM, August 21, 2021
Central New York
Xtreme Hike events take you through some of the most scenic trails in the nation. It's a journey of passion, determination and personal triumph, and an opportunity to make a difference in the lives of people with cystic fibrosis. Hikers participate in a training program to prepare them for this ultimate endurance challenge.
Rocky Mountain's Finest All Stars
August 21, 2021
From June-August, this group will compete for All-Star Status through an elevated fundraising campaign and unique engagement experiences. Participants will deepen their connection to the chapter and national organization and will have the opportunity to meet and network with other Rocky Mountain's Finest All-Stars.
Coach Randy & Laura Rahe Golf Classic
9:00 AM, August 27, 2021
Ogden Golf and Country Club
It's the 3rd annual Randy and Laura Rahe Golf Classic! Join Weber State Men's Basketball Coach Randy Rahe and his wife, Laura Rahe, for an unforgettable day of golf. This tournament is sure to sell out while helping the Cystic Fibrosis Foundation add tomorrows to the lives of those with cystic fibrosis.
Chicago CF Cycle for Life - Virtual
August 28, 2021
Greater Illinois - Chicago
Cystic Fibrosis Foundation
4550 Montgomery Ave.
Suite 1100 N
Bethesda, MD 20814
800-344-4823 (toll free)
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