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Peninsula Cystic Fibrosis Network - External Web Sites
           
    The web sites below will provide you with additional information to that which is contained within the Peninsula Cystic Fibrosis Network web site.
           
    The Cystic Fibrosis Trust - (http://www.cftrust.org.uk)
       
    The Cystic Fibrosis Trust is the charity promoting the interests of those with the UK's most common life-threatening inherited disease.
Their website includes information about living with CF day to day, CF forums and expert patients, fund-raising and CF Trust guidelines.
           
    The UK Cystic Fibrosis Microbiology Consortium - (http://www.cfmicrobiology.org.uk)  
         
    The UK Cystic Fibrosis Microbiology Consortium brings together scientists and clinicians with internationally recognised experience of CF
lung disease and complementary expertise.
           
    The Cystic Fibrosis Foundation - (http://cff.org)
     
    The mission of the Cystic Fibrosis Foundation, a nonprofit donor-supported organization in the USA, is to assure the development of the
means to cure and control cystic fibrosis and to improve the quality of life for those with the disease.
           
    The Royal Brompton & Harefield Hospital - (http://www.rbht.nhs.uk)
     
    The purpose of this document is to set out guidelines to ensure standardised care for children with cystic fibrosis looked after at the
Royal Brompton & Harefield NHS Trust and District General Hospitals on a shared care basis. They should be used as a guide only.
The Royal Brompton Hospital is a Specialist CF Centre as defined by the CF Trust Clinical Standards & Accreditation Group.
           
    Cystic Fibrosis Medicine - (http://www.cysticfibrosismedicine.com)
     
    Cystic Fibrosis Medicine has been set up with the aim of providing free information to professionals involved with the treatment of cystic
fibrosis. An open access (PUBLIC) section is also available to both patients and family. Cystic Fibrosis Medicine hopes to contribute to
individual unit protocols by bringing together medical and non-medical staff from around the world who wish to advance cystic fibrosis
care and contribute creatively to the long term development of this dedicated site.
           
           
           
Disclaimer: While efforts have been made to ensure that all the information published on this web site is correct, the authors take no responsibility for the accuracy of information, or for harm arising as a consequence of errors contained within this web site. If you have concerns regarding treatment, drugs or doses then consult your local CF consultant.