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Cystic Fibrosis Charities & Support |
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A-Z by country or region
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Adult CF Committee of Quebec (French)
Canadian Cystic Fibrosis Foundation - information for people with CF, parents and caregivers ( English & French)
Canadian Cystic Fibrosis Foundation local chapters
Cystic Fibrosis Association of Ireland
Mucone Xion - French website where you can share information about living with Cystic Fibrosis
German Cystic Fibrosis Association (Mukoviszidose e.V.)
Mukoland - my life with CF, treatment, family, sports, and German mailing list
Cystic Fibrosis Association of Ireland
Nederlandse Cystic Fibrosis Stichting - Dutch CF Foundation (Dutch)
Cystic Fibrosis Association of New Zealand - Support for people with CF with information about the disease
The Cystic Fibrosis Trust
Cystic Fibrosis Spanish Federation - Federacion Española contra la Fibrosis Quistica (English, Spanish, & German)
la Fibrosis Quistica - Asociación Madrileña Contra la Fibrosis Quística
RFCF, Riksförbundet Cystisk Fibros
CaFamily, UK
Cystic Fibrosis Trust, UK - research, fundraising, medical explanations and more
CF Dream Holidays - charity providing respite holidays for CF Children and families
United States
Charlotte's Angels - monthly events to raise money for the Cystic Fibrosis Foundation
Cystic Fibrosis Foundation - extensive information and resources including clinical trials, publications and low cost medication
Cystic Fibrosis Medicine - free information to patients & professionals concerned with the treatment of cystic fibrosis
CF Parents - Useful network for those US parents newly initiated into the world of Cystic Fibrosis
Cystic Fibrosis Research Center - news, events, chat rooms, support, information and question & answers about this disease
Cystic Fibrosis Resource Center - support community with books, medical news, articles and information, links, message boards
Health Boards Cystic Fibrosis - Forum for support, and for discussion of information, concerns, and treatment options
MyCysticFibrosis - Log on for Living With Cystic Fibrosis: personal management tools, health updates, articles, & personal support from on-site specialists
National Cystic Fibrosis Awareness Committee - serving to advance the public's awareness of Cystic Fibrosis
Cystic Fibrosis Medicine - free information to patients & professionals concerned with the treatment of cystic fibrosis
Cystic Fibrosis Research Inc - mission is to fund Cystic Fibrosis research and to offer educational and support programs
Reach For The Stars Foundation helping to aid and educate all those affected by Cystic Fibrosis, Bay Harbor Islands
Second Wind Lung Transplant Association - providing support, love, advocacy, education, information and guidance, Clearwater
Sunny Shores Sea Camp - summer camp for kids with Cystic Fibrosis in the Florida Keys staffed by volunteers
Reaching Out Foundation - programs, a personal story, general information, and how to donate
Wish for Wendy 2002 - softball tournament benefiting CF in honor of Wendy Carol Lipman, Atlanta
Cystic Fibrosis Research Center - news, events, chat rooms, support, information and question & answers about this disease
IRRI SHARK's Page - The "65 roses" story
Michigan Pulmonary Disease Inc - organization dedicated to enhancing lives of children and adults with Cystic Fibrosis
Family Relief Fund - provides financial assistance to families which have children with CF, Lebanon
Jake's Cystic Fibrosis Page - a personal web site with newsletter and chat
Official Site for CFF Jack Buck Book Event - Jack Buck, A Collection of Poems and Stories, with all proceeds going directly to Cystic Fibrosis Foundation
The New Jersey Organization of Cystic Fibrosis - New Jersey State charitable organization devoted to the battle against Cystic Fibrosis
Lungs for Life - providing financial assistance to cystic fibrosis and lung transplant patients, Rochester
The Spirit of Lo - engaging account about CF & the effects on an ordinary family
Living with Cystic Fibrosis - quality community site by computer specialist with CF, with advice on hospitalizations, relationships, and growing up with CF
Camp Funshine Home Page - free one-week summer camp for CF kids, seven or older, San Antonio
Utah Valley Institute of Cystic Fibrosis - promoting independent research to ameliorate cystic fibrosis
University Place Professional Firefighters Union Local 2105 Fund-Raiser - sponsor and active fund-raiser for the Cystic Fibrosis Foundation with two annual events