The method is discussed in the 2008 conference videos on cff.org. It is interesting but I still don't like the idea of the hospital, especially when they have never been hospitalized.
The method is discussed in the 2008 conference videos on cff.org. It is interesting but I still don't like the idea of the hospital, especially when they have never been hospitalized.
The method is discussed in the 2008 conference videos on cff.org. It is interesting but I still don't like the idea of the hospital, especially when they have never been hospitalized.
The method is discussed in the 2008 conference videos on cff.org. It is interesting but I still don't like the idea of the hospital, especially when they have never been hospitalized.
The method is discussed in the 2008 conference videos on cff.org. It is interesting but I still don't like the idea of the hospital, especially when they have never been hospitalized.
Obviously this is an emotional time for you as you sort through all of this new info. Once you are ready to learn more about CF, there is a LOT of info on the Cystic Fibrosis Foundation website: www.cff.org you will find info on the latest research (which is very exciting and encouraging) and...
Obviously this is an emotional time for you as you sort through all of this new info. Once you are ready to learn more about CF, there is a LOT of info on the Cystic Fibrosis Foundation website: www.cff.org you will find info on the latest research (which is very exciting and encouraging) and...
Obviously this is an emotional time for you as you sort through all of this new info. Once you are ready to learn more about CF, there is a LOT of info on the Cystic Fibrosis Foundation website: www.cff.org you will find info on the latest research (which is very exciting and encouraging) and...
Obviously this is an emotional time for you as you sort through all of this new info. Once you are ready to learn more about CF, there is a LOT of info on the Cystic Fibrosis Foundation website: www.cff.org you will find info on the latest research (which is very exciting and encouraging) and...
Obviously this is an emotional time for you as you sort through all of this new info. Once you are ready to learn more about CF, there is a LOT of info on the Cystic Fibrosis Foundation website: www.cff.org you will find info on the latest research (which is very exciting and encouraging) and...
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