Cystic Fibrosis Links

Here are some links for CF if you are interested. Cindy Lynn is on the second one.

The CFF (Cystic Fibrosis Foundation) is a national organization. It seeks to raise funds for research into CF. It also has lots of good links to other CF resources and good descriptions of what CF is and what it entails.

The NCFAC (National Cystic Fibrosis Awareness Committee) is a group of people either with CF, a parent of a child with CF, or a concerned person that is striving to get a national CF day. Check out their site for more info and ways of getting awareness of CF national.

CF101 for a crash course in CF.

More info available at this CF link

You can also get a lot more info at the Cystic Fibrosis Index of On-Line Resources

Another fabulous place for info on CF is the Cystic-L email list. You can join this list and talk with lots of CF patients and parents. They have helped us a lot. For more info, look at the Cystic-L homepage.