CF Websites

[anonymous]

Hi, There was recently a post that showed the CF Ireland site and I found it interesting to read information from other parts of the world. I am from Canada and our site is www.cysticfibrosis.ca. I thought it would be interesting if other people posted the sites from various places. In Quebec we also have (in French) http://www.aqfk.qc.ca/ or http://pages.infinit.net/aqfkmtl/Heather - Mom to Ashley

 

[anonymous]

one really useful one is www.cfww.org when i went to italy recently i found the page with all the italian info on it so i at least had some sort of contact details should problems arise over there!when it looked like i would be moving to france for the year (was studying french at uni but now cant do it coz of health probs) i contacted a doctor in france via the site and she was really helpful <img src="i/expressions/face-icon-small-smile.gif" border="0">the UK website is www.cftrust.org.ukand my personal website is www.pwcf.net (had to slip that in! <img src="i/expressions/face-icon-small-wink.gif" border="0">)

 

[anonymous]

sorry should have said that cfww stands for cf world wide. <img src="i/expressions/face-icon-small-happy.gif" border="0">

 

[oliver68]

for those who speak french, my web site is : http://oliver68.free.fr
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