List of cystic fibrosis organizations

The following organizations assist people with or do research into cystic fibrosis, a hereditary disease affecting the lungs and digestive system, causing progressive disability and sometimes early death.

• Cystic Fibrosis Australia^[1] (CFA), an Australian national organization aimed at raising awareness and education of cystic fibrosis through advocacy and research

• Cystic Fibrosis Trust, a UK charity providing research, information and care for people with cystic fibrosis
• European Cystic Fibrosis Society^[2] (ECFS), a Denmark-based organization of clinicians and scientists actively engaged in CF research, care and collaboration
• Association Grégory Lemarchal, a French organization dedicated to information outreach and research for cystic fibrosis, named after the French singer and Star Academy winner Grégory Lemarchal

• Canadian Cystic Fibrosis Foundation (CCFF), a Canada health organization funding cystic fibrosis research and care
• Cystic Fibrosis Foundation (CFF), a US non-profit providing the means to cure and control cystic fibrosis
• Cystic Fibrosis-Reaching Out Foundation^[3], a US-based network of information and support for people with CF and their families
• Boomer Esiason Foundation, a US-based organization supporting research aimed at finding a cure for cystic fibrosis as well providing education and raising quality of life for people with cystic fibrosis, named after Boomer Esiason, a former NFL quarterback, whose son Gunnar has cystic fibrosis.
• Lungs for Life Foundation^[4], a US-based organization focused on improving quality of life for people with CF through assistive services, education and research
• Elizabeth Nash Foundation^[5], a US-based organization focused on research, education and patient support, named after scientist Elizabeth Nash
• National Cystic Fibrosis Awareness Committee^[6] (NCFAC), a US-based group focused on increased public CF awareness through an annual national Cystic Fibrosis Awareness observance
• Rock CF Foundation^[7], a US-based non profit organization that uses the arts, entertainment, fashion and fitness to increase awareness and raise funds for cystic fibrosis. Founded by Emily Schaller.
• Liv for a Cure^[8], a US-based foundation dedicated to raising money for fight against Cystic Fibrosis.

• Cystic Fibrosis Worldwide^[9] (CFW), an international network concentrated on increasing quality of life and life expectancy for people with cystic fibrosis
• CysticFibrosis.com^[10], an internet information hub with support forums

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