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A cystic fibrosis information site. A guide to living with your sick or disabled child.
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Single mothers fight with Cystic Fibrosis and Marfans syndrome, affecting one lung.
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About a boy who has CF. A parent's personal weblog about the experiences of dealing with this chronic illness, and in depth information about CF.
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Billy Cook battled cystic fibrosis and died. The site generates funding for patients of this deadly disease.
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Site for boy with CF. Includes fund-raising items.
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Mother of a girl with CF has published a book which describes the story of her daughter's life with Cystic Fibrosis.
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Page by a woman with CF. Features links to various information on cystic fibrosis.
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This site is for children with cystic fibrosis designed by a man from the Netherlands with CF.
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Celine Dion lost her niece to CF and has supported the cause since.
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Site by a man with CF. Includes a list of symptoms and other information.
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site for boy with CF
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Site by girl with CF. Includes her hobbies, favorite music, favorite books and diagnosis story.
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Site by a Dutch woman with Cystic Fibrosis.
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Personal page by an aunt for her neice with CF.
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These pages are intended for world wide web as a resource of information on Cystic Fibrosis in English and Dutch they also link to other resources on Cystic Fibrosis.
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Site about a boy with CF.
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About a personal journey living with this disease, and alternative therapies used, besides antibiotics.
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The author son's journey of life with Cystic Fibrosis, with links to C/F information. Also original poem written to him.
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The personal website of a 31 year old man with CF. It provides current information about Cystic Fibrosis and links to other helpful sites.
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Cystic Fibrosis Page with the CFAM newsletter.
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Site by a woman waiting for a lung transplant.
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Site by Kathy known as "the Little Greek Girl" in some CF circles.
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Site about Shawn Hunter a 27 year-old man with CF who is waiting for a double lung transplant. Includes a journal of what is happening with Shawn.
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Personal page by a man with CF. Includes links to shop at various stores with a percent of the proceeds of sales going to the CFF.
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Page by a woman for her granddaughter who has cystic fibrosis.
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Site by a woman with CF - includes information on the disease.
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Patient with CF in Memphis, Tennessee.
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Site for a boy with Cystic Fibrosis.
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Site for a set of triplets one has CF.
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Site by a family from Belgum with a son with CF. Information on support from their community and fund-raising efforts. In English.
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About a little boy with CF.
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Site by a young man with CF.
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A girl who has Asthma, Diabetes, and Cystic Fibrosis, the number one genetic disease among Caucasians.
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Site for those wanting to learn about end stage. Not for someone whose child has been recently diagnosed. By a woman waiting for a lung transplant.
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Site by an English man with CF.
