Cystic Fibrosis: A Guide for Patient and Family by Dr. David Orenstein is very informative. It puts everything in laymans terms, and is easy to understand. My Daughters CF Clinic actually loans this book out to new patients.
Good luck!
Bubba, visit this website <a target=new class=ftalternatingbarlinklarge href="http://www.mycysticfibrosis.com/growing_older.asp">http://www.mycysticfibrosis.com/growing_older.asp</a> If you register as a user of mycysitfibrosis.com you can recieve this book for free. It is a great resource. Also, ask ask ask questions on this website. There is a whole lot to learn about CF and most questions are best answered by speaking with others. Way to be proactive!!
Breathing For a Living by Laura ROthenburg gives a really good look at transplant. I wouldn't recommmend it for someone who just got diagnosed or whose child just got diagnosed though, learn a little more about CF first.
The one that Reilly bug mentioned is brilliant. It goes through everything assosicated with cf, an excellent guide. Just check the year of publishing if you get it, because they update them, what with advancing treatments and everything.
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