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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CFsational: Women of WNY Celebration
12:00 PM, April 29, 2021
Western New York
With the health and well-being of the CF Community being the CF Foundation's top priority, the decision has been made to host the 2021 CFSational: Women of WNY Luncheon as a virtual celebration on Thursday, April 29th, 2021. This signature event recognizes women in our community who inspire others through their dedication and commitment to the CF Foundation.
Crawin' for the Cure
June 1, 2021
Texas Gulf Coast
As many of you are aware, the very successful “Cast for the Cure” and “Crawin' for the Cure” fundraisers in support of the Cystic Fibrosis Foundation (CFF) have been cancelled for this year due to the pandemic. While we're hopeful that we can resume our live crawfish cook-off in 2022, the ”Cast for the Cure” event has, unfortunately, been permanently ended.
Pipeline to a Cure
7:00 PM, August 7, 2021
Carolinas - Raleigh
We invite you to be a part of the virtual 10th Anniversary of Pipeline to a Cure. Please join us in celebrating the history of the Cystic Fibrosis Foundation while helping us accomplish all that we still need to do.
Grapes and Grain South Jersey
7:00 PM, September 2, 2021
Delaware Valley - Philadelphia
Join us for the 11th Annual Grapes and Grain South Jersey-A Virtual Tasting Experience! On Thursday, September 2, 2021 at 7:00 pm, from the comfort of your home, we will celebrate 11 years of finding a cure for CF, one sip at a time!
Red UN-Tie Ball
September 13, 2021
The Red UN-Tie Ball will take place over the span of one week. During that week, participants will receive many of the components of our traditional Red Tie Ball via e-mails and social media. The week-long virtual experience will include messages from our emcee, videos of our event chair and board chair and the powerful story of our Bid for a Cure speaker.
TBD, October 9, 2021
Date is subject to change. The Passion continues this year with an afternoon worth savoring. Join fellow foodies at the Sandlot Baltimore for an extraordinary culinary experience. Guests will feast on delectable bites by Baltimore's hottest chef talent and sip stylish cocktails and craft brews. With refreshing sights and sounds, relish in this epicurean adventure.
Cystic Fibrosis Foundation
4550 Montgomery Ave.
Suite 1100 N
Bethesda, MD 20814
800-344-4823 (toll free)
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