List of cystic fibrosis organizations
From Wikipedia, the free encyclopedia
The following organizations assist people with or conduct research on cystic fibrosis, a hereditary disease that affects the lungs and digestive system, causing progressive disability and often premature death.
- Cystic Fibrosis Australia (CFA),[1] an Australian national organization aimed at raising awareness and education of cystic fibrosis through advocacy and research
- CF Together (formerly Cystic Fibrosis Community Care),[2] the largest Australian organisation dedicated to raising awareness of CF, providing support services and advocacy to people living with CF, and funding research into CF. CF Together supports over 1,300 members and represents over 3,800 people living with CF in Australia.
- Cystic Fibrosis Western Australia (CFWA),[3] a Western Australian based organization that funds critical research and essential support services to improve the lives of children and adults afflicted by cystic fibrosis.
Europe
- Vaincre la Mucoviscidose,[4] a French based organization founded in 1965, providing research, health collaboration, social support and informations.
- Association Grégory Lemarchal,[5] a French organization dedicated to information outreach and research for cystic fibrosis, named after the French singer and Star Academy winner Grégory Lemarchal
- Build4Life,[6] a voluntary Irish Cystic Fibrosis charity that raises funds to develop CF facilities.
- Cystic Fibrosis Ireland (CFI),[7] a voluntary Irish organization set up in 1963 by parents, to aid patients with CF by improving facilities and treatments,[8]
- Child Health International (CHI),[9] a UK-based organization providing help especially in Eastern Europe, concentrating on low-cost, sustainable solutions based on teamwork and family involvement.
- Chloe Cotton Trust Fund,[10] a UK-based foundation to help support families and their children with cystic fibrosis.
- Cystic Fibrosis Foundation Slovenia, a Slovenian association providing information and care for CF patients and their families
- Nederlandse Cystic Fibrosis Stichting,[11] a Dutch organization providing research, information, and care for people and families with cystic fibrosis
- Cystic Fibrosis Trust,[12] a UK charity providing research, information and care for people with cystic fibrosis
- DCFH - Deutsche CF-Hilfe - Unterstützung für Menschen mit Mukoviszidose e.V.,[13] a German-based patient organization to support people with cystic fibrosis
- European Cystic Fibrosis Society (ECFS),[14] a Denmark-based organization of clinicians and scientists actively engaged in CF research, care and collaboration
- Mukolife.com is[15] a German social network for the CF community where members can post blogs, ask questions, chat, maintain a profile, contact others and search members. It is created by the CF community for the CF community.
- Cisztás Fibrózis Betegek Egyesülete (CFBE),[16] Association of cystic fibrosis patients organization to support people and family with cystic fibrosis.