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.
Guests of Gateway Chapter's Reach for the Stars Gala Raise $308,000 to Help Support the Search for a Cure
December 12, 2014
When guests of the Cystic Fibrosis Foundation Gateway Chapter’s 23rd annual Express Scripts Reach for the Stars Gala arrived at the Ritz Carlton Hotel in downtown St. Louis, they were whisked away to the whimsical world of The Big Easy. The event raised more than $308,000 to help support the Foundation’s lifesaving mission.
New York Giants' Josh Brown Invites Fans to 'help kick CF'
October 14, 2014
The Cystic Fibrosis Foundation would like to thank New York Giants placekicker Josh Brown and the island-style clothier, Tommy Bahama, who are teaming up to raise awareness and funds to support the mission of the CF Foundation through their campaign, the Goodfor3 Club.
Georgia Wine and Roses Gala Raises more than $347,000 to Support CF Foundation’s Mission
June 16, 2014
Touches of The Big Apple were seen throughout the Cystic Fibrosis Foundation Georgia Chapter’s New York City-themed Wine and Roses Gala, which raised more than $347,000 to help support the search for a cure in April.
Party City to Host Nationwide Campaign to Help Support the Search for a Cure
May 28, 2014
The Cystic Fibrosis Foundation thanks Party City for collecting donations from customers to help support the search for a cure at many of their party supply retail stores, now through June 23.
San Diego Women Raise $105,000 to Support Foundation’s Mission
May 20, 2014
Guests at the San Diego and Imperial County Chapter's 65 Roses Ladies Luncheon enjoyed the latest in art and fashion, raising $105,000 to help support the search for a cure for CF.
Lewis Black and Friends Host an Unforgettable Night to Help Power the Search for a Cure
May 16, 2014
Comedian and longtime friend of the Cystic Fibrosis Foundation, Lewis Black, brought together some of the biggest names in the entertainment business for a variety show that benefited the Cystic Fibrosis Foundation on May 5.
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Cystic Fibrosis Foundation
4550 Montgomery Ave.
Suite 1100 N
Bethesda, MD 20814
800-344-4823 (toll free)
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