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 cystic fibrosis patients and families face complicated issues related to getting the care they need. But CF Foundation Compass makes sure that no one has to do it alone.
For many people with cystic fibrosis, dealing with insurance is as much a part of living with the disease as nebulizers and vests. Many people with CF and their families face issues related to getting the care they need, but no one has to do it alone.
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.
1850 Lee Rd. Suite 111
Executive Director: Paul Gloersen
The Florida Chapter - Central Florida Office - Orlando of the Cystic Fibrosis Foundation welcomes you! Volunteers are the key to our success and the lifeblood of our organization. We have many opportunities for you to get involved. Your participation in any way will help us achieve our mission – finding a cure for all people with CF. Take a moment to check out our upcoming events and learn more.
Orlando 2019 Great Strides
8:00 AM, April 27, 2019
Bill Frederick Park at Turkey Lake
Florida - Central Florida
Lake Nona 2019 Great Strides
9:00 AM, May 4, 2019
Brevard County 2019 Great Strides
8:00 AM, May 18, 2019
6:30 PM, August 15, 2019
Orlando's Finest 2019 event celebrates top young business professionals and emerging leaders in the forefront of their industries within the greater Orlando community. Criteria is based on excellence in their chosen profession and interest in contributing to our community.
Orlando CF Climb 2019
10 AM, September 28, 2019
Orlando World Center Marriott
Florida - Orlando
CF Climb is a challenging and unique fitness event where participants climb the flights of stairs in a tall building or around stadiums in a test of endurance and time. Whether climbing to improve timing or to simply cross the finish line, this event is a great way to spend the day with co-workers, friends or family while “Adding Tomorrows” for people with cystic fibrosis. At the end of the climb, participants celebrate at the survival party with delicious food and great entertainment.
Central Florida CF Cycle for Life 2019
8:00 AM, November 10, 2019
Georgia Avenue DeLand
Greg Warmoth Holiday Classic
8:00 AM, December 16, 2019
Heathrow Country Club
The Cystic Fibrosis Foundation's Greg Warmoth Holiday Classic will make it's return to Heathrow Country Club. This year's golf outing promises to be a great event, filled with good friends and great golf!
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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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