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Personal Pages (30)
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A cystic fibrosis information site. A guide to living with your sick or disabled child.
http://www.specialchild.co.uk/
Single mothers fight with Cystic Fibrosis and Marfans syndrome, affecting one lung.
http://www.angelfire.com/ms2/CysticFibrosisMarfan/index.html
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.
http://www.azerscfwebsite.com/
Billy Cook battled cystic fibrosis and died. The site generates funding for patients of this deadly disease.
http://www.billycook.com
Pat Cuckney has published a book which describes the story of her daughter's life with cystic fibrosis.
http://www.cuckney.pwp.blueyonder.co.uk/home/cfhome.htm
Page by a woman with CF. Features links to various information on cystic fibrosis.
http://www3.nbnet.nb.ca/normap/CF.htm
This site is for children with cystic fibrosis designed by a man from the Netherlands with CF.
http://members.tripod.com/~jtatton/index.html
Site by a man with CF. Includes a list of symptoms and other information.
http://www.members.tripod.com/chuckmayer/cf.html
Site by girl with CF. Includes her hobbies, favorite music, favorite books and diagnosis story.
http://crayzray.tripod.com/clpage/cl.htm
Site by a Dutch woman with Cystic Fibrosis.
http://www.lintje.com/cfeng.htm
Personal page by an aunt for her niece with CF.
http://members.tripod.com/~blackwolf54/index.html
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.
http://cfinformer.tripod.com/
Site about a boy with CF.
http://personalpages.tds.net/~dhargrov/
About a personal journey living with this disease, and alternative therapies used, besides antibiotics.
http://www.angelfire.com/ok4/cfgen/
Cystic Fibrosis Page with the CFAM newsletter.
http://www.angelfire.com/mo2/cf/index.html
A personal look at the disease cystic fibrosis from a bloggers perspective.
http://pegsoninthepresent.com
Sally describes the need for children to be given more information on genetic disorders affecting family members.
http://www.tellingstories.nhs.uk/transcript.asp?id=51
Site by a family from Belgium with a son with CF. Information on support from their community and fund-raising efforts. In English.
http://users.skynet.be/tildonk_tegen_muco/tildonk1.htm
Dedicated to Grace Beshore and her battle with cystic fibrosis.
http://www.dayspainsurance.com/wpwfg/
Rachel describes the difficulties she has experienced as a mother of two children with cystic fibrosis and the need for families to receive accurate and useful information from healthcare professionals.
http://www.tellingstories.nhs.uk/transcript.asp?id=20
Last Updated: 2007-09-06 08:42:39
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The content of this directory is based on the Open Directory and has been modified by AllMusicSearch.com editors
