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Cystic Fibrosis Charities & Support |
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A-Z by country or region
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Austria Belgium
Association Belge de Lutte contre la Mucovisidose Belgian Cystic Fibrosis Association (Flemish & French) 
Bermuda Brazil
Canada Adult CF Committee of Quebec (French) Association Quebecoise de Fibrose Kystique, Canada, (French)
Canadian Cystic Fibrosis Foundation - information for people with CF, parents and caregivers Canadian Cystic Fibrosis Foundation local chapters China Croatia Czech Republic Denmark Landsforeningen til Bekæmpelse af Cystisk Fibrose, Danish CF Association Eastern Europe Eire Cystic Fibrosis Association of Ireland Europe Finland France
Mucone Xion - French website where you can share information about living with Cystic Fibrosis S.O.S. Mucoviscidose - French CF National Association
Germany
German CF Foundation - CF-Selbsthilfe Bundesverband e.V. (German) 
German Cystic Fibrosis Association (Mukoviszidose e.V.) Mukoviszidose e.V. - German CF Association
Mukoland - my life with CF, treatment, family, sports, and German mailing list
Greece
Hong Kong
Iceland
India
Ireland Cystic Fibrosis Association of Ireland Israel
Italy
Japan
Korea, South
Luxembourg
Mexico Middle East Netherlands
Cystic Fibrosis Worldwide, Netherlands
Nederlandse Cystic Fibrosis Stichting - Dutch CF Foundation (English & Dutch) New Zealand
Cystic Fibrosis Association of New Zealand - Support for people with CF with information about the disease Norway The Cystic Fibrosis Trust Pakistan
Poland
Portugal
Russia
Saudi Arabia
Singapore
South Africa
South & Central America
South Korea
Spain Cystic Fibrosis Spanish Federation - Federacion Española contra la Fibrosis Quistica (English, Spanish, & German) la Fibrosis Quistica - Asociación Madrileña Contra la Fibrosis Quística Sweden RFCF, Riksförbundet Cystisk Fibros Switzerland
Taiwan
Thailand
Turkey
Ukraine
United Kingdom
CaFamily, UK 
Cystic Fibrosis Holiday Fund for children - NR
Cystic Fibrosis Trust, UK - research, fundraising, medical explanations and more CF sponsored walk through Snowdonia - Please sponsor Ross Kempson and his brother as they climb their way through Snowdonia for CF CF Dream Holidays - charity providing respite holidays for CF Children and families Salvay Healthcare UK CysticFibrosis.co.uk - excellent support site with useful source of information for cystic fibrosis patients, parents, doctors and carers 
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 CysticFibrosis.com - an internet community and unparalleled CF information resource
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 Lungs for Brooke - Friends and family of Brooke Butner are asking for your help in raising money with useful information 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 The National Information Center for Children and Youth with Disabilities The National Women's Health Information Center
Alabama
Alaska
Iditarod 2003, Mush On For Cystic Fibrosis - Tim and Lori Layne are running their dog sled team 1,150 miles from Anchorage to Nome to raise money for CF Arizona
Arkansas California
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 Milan Foundation - created in the name of Milan Brown. Calendar, stories, poems, and donations, Beverley Hills Special Child: For Parents and Caregivers of Children with Special Needs, Santa Clarita Colorado
Connecticut
Delaware
Florida 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 Georgia Camp Wak-n-Hak - week's overnight camping for children with CF with programming and medical care included, Camp Twin Lakes, Rutledge
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 Hawaii
Idaho
Illinois
Indiana A Message from above - dedicated to the memory of Heather Kay Mattke and Holly Kay (Mattke) Wheelock Iowa
Kansas Richard Shannon Lung Transplant Fund - a fund raiser is ongoing to pay for expenses beyond insurance provision Kentucky
Louisiana
Maine
Maryland Cystic Fibrosis Research Center - news, events, chat rooms, support, information and question & answers about this disease IRRI SHARK's Page - The "65 roses" story Massachusetts
Federation for Children with Special Needs NR
Michigan Michigan Pulmonary Disease Inc - organization dedicated to enhancing lives of children and adults with Cystic Fibrosis Minnesota
Mississippi
Missouri 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 Montana
Nebraska
Nevada
New Hampshire
New Jersey The New Jersey Organization of Cystic Fibrosis - New Jersey State charitable organization devoted to the battle against Cystic Fibrosis New Mexico
New York Corrine's Pride a 5K run for Cystic Fibrosis - annual 5K race inspired by Corrine who was diagnosed with CF, Staten Island Lungs for Life - providing financial assistance to cystic fibrosis and lung transplant patients, Rochester North Carolina
North Dakota
Ohio
Oklahoma The Spirit of Lo - engaging account about CF & the effects on an ordinary family Oregon
Pennsylvania Living with Cystic Fibrosis - quality community site by computer specialist with CF, with advice on hospitalizations, relationships, and growing up with CF Pennsylvania Cystic Fibrosis. Inc. - funding for Pennsylvania families affected by CF and for most promising US CF research projects (restricted) Rhode Island
South Carolina
South Dakota
Tennessee Cindy's Friends - Walking for Cystic Fibrosis, Working for Cure Found - Information, progress, and fundraising effort, Nashville Sevier County Team CF - formed in 2000 by Jim Deanda and Barbara Gray, CF parents, who last year raised over $40,000 for CF research Texas Camp Funshine Home Page - free one-week summer camp for CF kids, seven or older, San Antonio Utah Utah Valley Institute of Cystic Fibrosis - promoting independent research to ameliorate cystic fibrosis Vermont
Virginia
Washington University Place Professional Firefighters Union Local 2105 Fund-Raiser - sponsor and active fund-raiser for the Cystic Fibrosis Foundation with two annual events Washington, D.C.
The National Information Center for Children and Youth with Disabilities West Virginia
Wisconsin How to handle living with Cystic Fibrosis - a personal community site of note with medical issues, tips and advice Wyoming
International