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Your CF doctor may prescribe many medications to help keep your lungs clear, prevent or fight infections and, for some people, help correct the underlying cause of the disease. Medications that people need to fight infections for a long time may require additional devices, such as PICCs and ports.
Many people with cystic fibrosis face the possibility of a lung transplant. Lung transplantation can extend and improve your quality of life, but it involves an extensive evaluation process and a commitment to living the lifestyle required to keep your new lungs healthy.
For many people with cystic fibrosis, dealing with insurance is as much a part of living with the disease as are nebulizers and vests. Learning more about insurance can help make sure you can get the care you need.
Each year, hundreds of volunteers from across the country participate in advocacy events that help state and federal policymakers and decision-makers understand the complexities of living with cystic fibrosis and the importance of having access to affordable, adequate care and supporting research and drug development.
The latest news from the Cystic Fibrosis Foundation.
BreatheCon is a unique event to virtually gather with other adults with CF in a welcoming, inclusive space where you can be your authentic self.
Virtual
Virtual
BreatheCon is a unique event to virtually gather with other adults with CF in a welcoming, inclusive space where you can be your authentic self.
Virtual
Virtual
ResearchCon is for everyone with a personal or professional connection to cystic fibrosis to learn and discuss CF-related science and care alongside others living with and studying the disease.
Virtual
Virtual
ResearchCon is for everyone with a personal or professional connection to cystic fibrosis to learn and discuss CF-related science and care alongside others living with and studying the disease.
Virtual
Virtual