Cystic Fibrosis is
New Zealand's most common life-threatening inherited condition and the
CF Association is the only national organisation
dedicated to all aspects
of the condition.

Social Networks

The advent of social networking sites has been a great boon for people with Cystic Fibrosis, as it means that they can maintain their connectivity with their peers, and not have to worry about cross-infection issues.

The Cystic Fibrosis Association of New Zealand supports social networking by maintaining four facebook pages, each aimed a different sector of our community, producing an informative and newsy magazine, CF News four times per year, issuing CF Talk, a news magazine for CF Adults, and Kids Club News.

 

An open page where you can be kept up-to-date with the goings on of the Association can be found at

 

 

http://www.facebook.com/pages/Cystic-Fibrosis-NZ/171499682890863

 

 

   Adults of the CF Community

There are two pages for Adults in the CF Community:  CF Adults - Closed Group, and CF Carers & Supporters.  For more information on these groups, please go to Adult Networks 

  

       CF Teen Talk

A group for young people with Cystic Fibrosis 13-18 years old, to share experiences and support for hte journey with CF (and everything else that life throws at you).  This site is moderated by Cystic Fibrosis NZ.

To join please contact Kate Russell

  
 

 http://www.facebook.com/#!/groups/168692363161069/

 

 

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